The interface between assisted reproductive technologies ( ART) and genetics comprises several sensitive and important issues that affect infertile couples, families with severe genetic diseases, potential children, professionals in ART and genetics, health care, researchers and the society in general. Genetic causes have a considerable involvement in infertility. Genetic conditions may also be transmitted to the offspring and hence create transgenerational infertility or other serious health problems. Several studies also suggest a slightly elevated risk of birth defects in children born following ART. Preimplantation genetic diagnosis (PGD) has become widely practiced throughout the world for various medical indications, but its limits are being debated. The attitudes towards ART and PGD vary substantially within Europe. The purpose of the present paper was to outline a framework for development of guidelines to be issued jointly by European Society of Human Genetics and European Society of Human Reproduction and Embryology for the interface between genetics and ART. Technical, social, ethical and legal issues of ART and genetics will be reviewed.
Handyside A. H., Kontogianni E. H., Hardy K., Winston R. M. L., Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification, 10.1038/344768a0
Boyle Karen Elizabeth, Vlahos Nikos, Jarow Jonathan P, Assisted reproductive technology in the new millennium: part II, 10.1016/j.urology.2003.07.015
Knoppers Bartha M., Isasi Rosario M., Regulatory approaches to reproductive genetic testing, 10.1093/humrep/deh505
Sermon K., Moutou C., Harper J., Geraedts J., Scriven P., Wilton L., Magli M.C., Michiels A., Viville S., De Die C., ESHRE PGD Consortium data collection IV: May–December 2001, 10.1093/humrep/deh552
Wilton Leeanda, Preimplantation genetic diagnosis for aneuploidy screening in early human embryos: a review, 10.1002/pd.388
Adashi EY, RBM (online), 7, 515 (2003)
Bonduelle M., Wennerholm U.-B., Loft A., Tarlatzis B.C., Peters C., Henriet S., Mau C., Victorin-Cederquist A., Van Steirteghem A., Balaska A., Emberson J.R., Sutcliffe A.G., A multi-centre cohort study of the physical health of 5-year-old children conceived after intracytoplasmic sperm injection, in vitro fertilization and natural conception, 10.1093/humrep/deh592
Hansen Michèle, Bower Carol, Milne Elizabeth, de Klerk Nicholas, J.Kurinczuk Jennifer, Assisted reproductive technologies and the risk of birth defects—a systematic review, 10.1093/humrep/deh593
Klemetti Reija, Gissler Mika, Sevón Tiina, Koivurova Sari, Ritvanen Annukka, Hemminki Elina, Children born after assisted fertilization have an increased rate of major congenital anomalies, 10.1016/j.fertnstert.2005.03.085
Ludwig M, Increased prevalence of imprinting defects in patients with Angelman syndrome born to subfertile couples, 10.1136/jmg.2004.026930
Min J. K., What is the most relevant standard of success in assisted reproduction? The singleton, term gestation, live birth rate per cycle initiated: the BESST endpoint for assisted reproduction, 10.1093/humrep/deh028
Aittomaki K., Safety issues in assisted reproduction technology: Should ICSI patients have genetic testing before treatment? A practical proposition to help patient information, 10.1093/humrep/deh100
Geraedts Joep P. M., Harper Joyce, Braude Peter, Sermon Karen, Veiga Anna, Gianaroli Luca, Agan Noelle, Munné Santiago, Gitlin Sue, Blenow Elisabeth, de Boer Kylie, Hussey Nicole, Kanavakis Emmanuel, Lee Soo-Huan, Viville Stéphane, Krey Lewis, Ray Pierre, Emiliani Serena, Hsien Liu Yung, Vermeulen Stefan, Preimplantation genetic diagnosis (PGD), a collaborative activity of clinical genetic departments and IVF centres : COLLABORATIVE ACTIVITY OF CLINICAL GENETIC DEPARTMENTS AND IVF CENTRES IN PGD, 10.1002/pd.249
Houmard B, Infertility treatment and informed consent: current practices of reproductive endocrinologists, 10.1016/s0029-7844(98)00389-5
Ayhan Ali, Salman Mehmet Coskun, Celik Husnu, Dursun Polat, Ozyuncu Ozgur, Gultekin Murat, Association between fertility drugs and gynecologic cancers, breast cancer, and childhood cancers, 10.1111/j.0001-6349.2004.00669.x
Schieve Laura A., Rasmussen Sonja A., Reefhuis Jennita, Risk of birth defects among children conceived with assisted reproductive technology: providing an epidemiologic context to the data, 10.1016/j.fertnstert.2005.04.066
Sutcliffe Alastair G., Congenital anomalies and assisted reproductive technology: more of the same, 10.1016/j.fertnstert.2005.04.067
Olivennes Francois, Do children born after assisted reproductive technology have a higher incidence of birth defects?, 10.1016/j.fertnstert.2005.05.044
Michie Susan, McDonald Valerie, Marteau Theresa M., Genetic counselling: information given, recall and satisfaction, 10.1016/s0738-3991(97)00050-5
Foresta Carlo, Ferlin Alberto, Gianaroli Luca, Dallapiccola Bruno, Guidelines for the appropriate use of genetic tests in infertile couples, 10.1038/sj.ejhg.5200805
Vogt Peter H., Genomic heterogeneity and instability of the AZF locus on the human Y chromosome, 10.1016/j.mce.2004.06.008
Foresta Carlo, Garolla Andrea, Bartoloni Lucia, Bettella Andrea, Ferlin Alberto, Genetic Abnormalities among Severely Oligospermic Men Who Are Candidates for Intracytoplasmic Sperm Injection, 10.1210/jc.2004-1469
Bourrouillou G, Prog Urol, 2, 189 (1992)
SEIFER, AMAT, DELGADO-VISCOGLIOSI, BOUCHER, BIGNON, Screening for microdeletions on the long arm of chromosome Y in 53 infertile men, 10.1046/j.1365-2605.1999.00161.x
Foresta C., Prognostic value of Y deletion analysis: The role of current methods, 10.1093/humrep/16.8.1543
Tiepolo L., Zuffardi Orsetta, Localization of factors controlling spermatogenesis in the nonfluorescent portion of the human y chromosome long arm, 10.1007/bf00278879
Vogt P, RBM (online), 10, 11 (2005)
Johnson Mark D, Genetic risks of intracytoplasmic sperm injection in the treatment of male infertility: recommendations for genetic counseling and screening, 10.1016/s0015-0282(98)00209-x
Bernardini L., Borini A., Preti S., Conte N., Flamigni C., Capitanio G. L., Venturini P. L., Study of aneuploidy in normal and abnormal germ cells from semen of fertile and infertile men, 10.1093/humrep/13.12.3406
Pang M.G., Detection of aneuploidy for chromosomes 4, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 21, X and Y by fluorescence in-situ hybridization in spermatozoa from nine patients with oligoasthenoteratozoospermia undergoing intracytoplasmic sperm injection, 10.1093/humrep/14.5.1266
Burrello N., Lower sperm aneuploidy frequency is associated with high pregnancy rates in ICSI programmes, 10.1093/humrep/deg299
Ferlin A., Garolla A., Foresta C., Chromosome abnormalities in sperm of individuals with constitutional sex chromosomal abnormalities, 10.1159/000086905
Poulakis Vassilis, Witzsch Ulrich, Diehl Wolfgang, de Vries Rachelle, Becht Eduard, Trotnow Siegfried, Birth of two infants with normal karyotype after intracytoplasmic injection of sperm obtained by testicular extraction from two men with nonmosaic Klinefelter’s syndrome, 10.1016/s0015-0282(01)02830-8
Rubio C., Gil-Salom M., Simón C., Vidal F., Rodrigo L., Mínguez Y., Remohí J., Pellicer A., Incidence of sperm chromosomal abnormalities in a risk population: relationship with sperm quality and ICSI outcome, 10.1093/humrep/16.10.2084
Aran Begoña, Blanco Joan, Vidal Francesca, Vendrell Josep Ma, Egozcue Susana, Barri Pere N, Egozcue Josep, Veiga Anna, Screening for abnormalities of chromosomes X, Y, and 18 and for diploidy in spermatozoa from infertile men participating in an in vitro fertilization-intracytoplasmic sperm injection program, 10.1016/s0015-0282(99)00307-6
Egozcue J., Blanco J., Anton E., Egozcue S., Sarrate Z., Vidal F., Genetic Analysis of Sperm and Implications of Severe Male Infertility—A Review, 10.1016/s0143-4004(03)00186-3
Anguiano A., Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis, 10.1001/jama.267.13.1794
Weiske W.-H., Salzler N., Schroeder-Printzen I., Weidner W., Clinical findings in congenital absence of the vasa deferentia, 10.1046/j.1439-0272.2000.00093.x
McCallum T.J., Unilateral renal agenesis associated with congenital bilateral absence of the vas deferens: phenotypic findings and genetic considerations, 10.1093/humrep/16.2.282
Källén Bengt, Finnström Orvar, Nygren Karl Gösta, Olausson Petra Otterblad, In vitro fertilization (IVF) in Sweden: Risk for congenital malformations after different IVF methods : Congenital Malformations and IVF, 10.1002/bdra.20107
Egozcue J., Sarrate Z., Codina-Pascual M., Egozcue S., Oliver-Bonet M., Blanco J., Navarro J., Benet J., Vidal F., Meiotic abnormalities in infertile males, 10.1159/000086907
Arán B, Reprod Biomed (online), 8, 470 (2004)
Jequier A. M., Clinical andrology--still a major problem in the treatment of infertility, 10.1093/humrep/deh269
Palermo G. D., Colombero L. T., Hariprashad J. J., Schlegel P. N., Rosenwaks Z., Chromosome analysis of epididymal and testicular sperm in azoospermic patients undergoing ICSI, 10.1093/humrep/17.3.570
Fertil Steril, 77, S1 (2002)
Thurin Ann, Hausken Jon, Hillensjö Torbjörn, Jablonowska Barbara, Pinborg Anja, Strandell Annika, Bergh Christina, Elective Single-Embryo Transfer versus Double-Embryo Transfer in in Vitro Fertilization, 10.1056/nejmoa041032
Martikainen Hannu, Tiitinen Aila, Tomás Candido, Tapanainen Juha, Orava Mauri, Tuomivaara Leena, Vilska Sirpa, Hydén-Granskog Christel, Hovatta Outi, One versus two embryo transfer after IVF and ICSI: a randomized study, 10.1093/humrep/16.9.1900
Bergh C., Chromosomal abnormality rate in human pre-embryos derived from in vitro fertilization cycles cultured in the presence of Follicular-Fluid Meiosis Activating Sterol (FF-MAS), 10.1093/humrep/deh388
de Boer Kylie A, Catt James W, Jansen Robert P.S, Leigh Don, McArthur Steven, Moving to blastocyst biopsy for preimplantation genetic diagnosis and single embryo transfer at sydney IVF, 10.1016/j.fertnstert.2003.11.064
Reprod Biomedicine (online), 9, 430 (2004)
Strom C. M., Levin R., Strom S., Masciangelo C., Kuliev A., Verlinsky Y., Neonatal Outcome of Preimplantation Genetic Diagnosis by Polar Body Removal: The First 109 Infants, 10.1542/peds.106.4.650
Antczak M., Van Blerkom J., Temporal and spatial aspects of fragmentation in early human embryos: possible effects on developmental competence and association with the differential elimination of regulatory proteins from polarized domains, 10.1093/humrep/14.2.429
Ziebe S., FISH analysis for chromosomes 13, 16, 18, 21, 22, X and Y in all blastomeres of IVF pre-embryos from 144 randomly selected donated human oocytes and impact on pre-embryo morphology, 10.1093/humrep/deg489
Milki Amin A, Jun Sunny H, Hinckley Mary D, Behr Barry, Giudice Linda C, Westphal Lynn M, Incidence of monozygotic twinning with blastocyst transfer compared to cleavage-stage transfer, 10.1016/s0015-0282(02)04754-4
Scriven P.N., Robertsonian translocations--reproductive risks and indications for preimplantation genetic diagnosis, 10.1093/humrep/16.11.2267
Sermon Karen, De Rijcke Martine, Lissens Willy, De Vos Anick, Platteau Peter, Bonduelle Maryse, Devroey Paul, Van Steirteghem André, Liebaers Inge, Preimplantation genetic diagnosis for Huntington's disease with exclusion testing, 10.1038/sj.ejhg.5200865
Moutou Céline, Gardes Nathalie, Viville Stéphane, New tools for preimplantation genetic diagnosis of Huntington's disease and their clinical applications, 10.1038/sj.ejhg.5201291
Stern Harvey J., Harton Gary L., Sisson Michael E., Jones Shirley L., Fallon Lee A., Thorsell Lilli P., Getlinger Michael E., Black Susan H., Schulman Joseph D., Non-disclosing preimplantation genetic diagnosis for Huntington disease, 10.1002/pd.359
Braude Peter R., de Wert Guido M. W. R., Evers-Kiebooms Gerry, Pettigrew Rachel A., Geraedts Joep P. M., Non-disclosure preimplantation genetic diagnosis for Huntington's disease: practical and ethical dilemmas, 10.1002/(sici)1097-0223(199812)18:13<1422::aid-pd499>3.0.co;2-r
Munne S, Reprod Biomed (online), 4, 183 (2002)
Wilton Leeanda, Preimplantation genetic diagnosis and chromosome analysis of blastomeres using comparative genomic hybridization, 10.1093/humupd/dmh050
Briggs DA, Power NJ, Lamb V, Rutherford AJ, Gosden RG, Amplification of DNA sequences in polar bodies from human oocytes for diagnosis of mitochondrial disease, 10.1016/s0140-6736(00)02171-1
Kuliev A, Obstet Gynecol, 17, 179 (2005)
Goldman JM, , Schmitz N, Niethammer D, Gratwohl A, Allogeneic and autologous transplantation for haematological diseases, solid tumours and immune disorders: current practice in Europe in 1998, 10.1038/sj.bmt.1701089
Pennings G., Schots R., Liebaers I., Ethical considerations on preimplantation genetic diagnosis for HLA typing to match a future child as a donor of haematopoietic stem cells to a sibling, 10.1093/humrep/17.3.534
Fiorentino F., Development and clinical application of a strategy for preimplantation genetic diagnosis of single gene disorders combined with HLA matching, 10.1093/molehr/gah055
Van de Velde H., Novel universal approach for preimplantation genetic diagnosis of -thalassaemia in combination with HLA matching of embryos, 10.1093/humrep/deh153
Kahraman S, Reprod Biomed (online), 9, 529 (2004)
Verlinsky Yury, Cohen Jacques, Munne Santiago, Gianaroli Luca, Simpson Joe Leigh, Ferraretti Anna Pia, Kuliev Anver, Over a decade of experience with preimplantation genetic diagnosis: A multicenter report, 10.1016/j.fertnstert.2003.09.082
De Die-Smulders C, Ned Tijdschr v Geneesk, 148, 2491 (2004)
Lavery S.A., Preimplantation genetic diagnosis: patients' experiences and attitudes, 10.1093/humrep/17.9.2464
Katz Mandy G., Fitzgerald Lara, Bankier Agnes, Savulescu Julian, Cram David S., Issues and concerns of couples presenting for preimplantation genetic diagnosis (PGD), 10.1002/pd.498
Pennings Guido, Legal harmonization and reproductive tourism in Europe, 10.1093/humrep/deh486
King DS, J Med Ethics, 25, 176 (1999)
Vance A., Zouves C., The Importance of Family History Risk Assessment in the Infertility Setting, 10.1016/j.fertnstert.2005.07.305
Janssens P. M.W., No reason for a reduction in the number of offspring per sperm donor because of possible transmission of autosomal dominant diseases, 10.1093/humrep/deg137
Jacquard A, Ann Génét, 19, 229 (1976)
Eydoux P., How can the genetic risks of embryo donation be minimized?: Proposed guidelines of the French Federation of CECOS (Centre d'Etude et de Conservation des Oeufs et du Sperme), 10.1093/humrep/deh328
Shiloh S, Psychol Health, 3, 45 (1989)
Godard Béatrice, Kääriäinen Helena, Kristoffersson Ulf, Tranebjaerg Lisbeth, Coviello Domenico, Aymé Ségolène, Provision of genetic services in Europe: current practices and issues, 10.1038/sj.ejhg.5201111
Emery M., Results from a prospective, randomized, controlled study evaluating the acceptability and effects of routine pre-IVF counselling, 10.1093/humrep/deg501
van Zuuren F.J., van Schie E.C.M., van Baaren N.K., Uncertainty in the information provided during genetic counseling, 10.1016/s0738-3991(97)00052-9
Welkenhuysen Myriam, Evers-Kiebooms Gerry, d’Ydewalle Géry, The language of uncertainty in genetic risk communication: framing and verbal versus numerical information, 10.1016/s0738-3991(00)00161-0
Elwyn G., Shared decision making and non-directiveness in genetic counselling, 10.1136/jmg.37.2.135
Adrian Edwards, Glyn Elwyn, Judith, Presenting Risk Information A Review of the Effects of Framing and other Manipulations on Patient Outcomes, 10.1080/10810730150501413
M. Marteau Theresa, Nippert Irma, Hall Sue, Limbert Caroline, Reid Margaret, Bobrow Martin, Cameron Alan, Cornel Martina, van Diem Mariet, Eiben Bernd, García-Miñaur Sixto, Goujard Janine, Kirwan Donna, McIntosh Karen, Soothill Peter, Verschuuren-Bemelmans Corien, de Vigan Catherine, Walkinshaw Stephen, Abramsky Lenore, Louwen Frank, Miny Peter, Horst Jürgen, Outcomes of pregnancies diagnosed with Klinefelter syndrome: the possible influence of health professionals† : COUNSELLING AND KLINEFELTER SYNDROME, 10.1002/pd.374
Lambert R. D., Safety issues in assisted reproductive technology: Aetiology of health problems in singleton ART babies, 10.1093/humrep/deg361
Wennerholm UB, RBM (online), 7, 515 (2003)
Hazekamp J., Bergh C., Wennerholm U.-B., Hovatta O., Karlström P.O., Selbing A., Avoiding multiple pregnancies in ART, 10.1093/humrep/15.6.1217
Shenfield F, RBM (online), 7, 515 (2003)
Vilska S., Tiitinen A., Hydén-Granskog C., Hovatta O., Elective transfer of one embryo results in an acceptable pregnancy rate and eliminates the risk of multiple birth, 10.1093/humrep/14.9.2392
Salumets A., Early cleavage predicts the viability of human embryos in elective single embryo transfer procedures, 10.1093/humrep/deg184
Slotnick R. N., Ortega Joanna E., Monoamniotic twinning and zona manipulation: A survey of U.S. IVF centers correlating zona manipulation procedures and high-risk twinning frequency, 10.1007/bf02066168
Schieve Laura A, Meikle Susan F, Peterson Herbert B, Jeng Gary, Burnett Nancy M, Wilcox Lynne S, Does assisted hatching pose a risk for monozygotic twinning in pregnancies conceived through in vitro fertilization?, 10.1016/s0015-0282(00)00602-6
Braude P., Assisted conception. III--Problems with assisted conception, 10.1136/bmj.327.7420.920
Hreinsson J., Recombinant LH is equally effective as recombinant hCG in promoting oocyte maturation in a clinical in-vitro maturation programme: a randomized study, 10.1093/humrep/deg422
Gauthier E., Paoletti X., Clavel-Chapelon F., Breast cancer risk associated with being treated for infertility: results from the French E3N cohort study, 10.1093/humrep/deh422
Brinton Louise A., Lamb Emmet J., Moghissi Kamran S., Scoccia Bert, Althuis Michelle D., Mabie Jerome E., Westhoff Carolyn L., Ovarian Cancer Risk After the Use of Ovulation-Stimulating Drugs : , 10.1097/01.aog.0000128139.92313.74
Hansen Michèle, Kurinczuk Jennifer J., Bower Carol, Webb Sandra, The Risk of Major Birth Defects after Intracytoplasmic Sperm Injection and in Vitro Fertilization, 10.1056/nejmoa010035
Schieve Laura A., Meikle Susan F., Ferre Cynthia, Peterson Herbert B., Jeng Gary, Wilcox Lynne S., Low and Very Low Birth Weight in Infants Conceived with Use of Assisted Reproductive Technology, 10.1056/nejmoa010806
Pinborg Anja, Loft Anne, Andersen Anders Nyboe, Neonatal outcome in a Danish national cohort of 8602 children born after in vitro fertilization or intracytoplasmic sperm injection: the role of twin pregnancy, 10.1111/j.0001-6349.2004.00476.x
Wennerholm U.-B., Cryopreservation of embryos and oocytes: obstetric outcome and health in children, 10.1093/humrep/15.suppl_5.18
Koivurova S., Neonatal outcome and congenital malformations in children born after in-vitro fertilization, 10.1093/humrep/17.5.1391
Panel Reviews Health Effects Data for Assisted Reproductive Technologies, 10.1001/jama.292.24.2961
Lidegaard Øjvind, Pinborg Anja, Andersen Anders Nyboe, Imprinting diseases and IVF: Danish National IVF cohort study, 10.1093/humrep/deh714
Moll Annette C, Imhof Saskia M, Cruysberg Johannes RM, Schouten-van Meeteren Antoinette YN, Boers Maarten, van Leeuwen Flora E, Incidence of retinoblastoma in children born after in-vitro fertilisation, 10.1016/s0140-6736(03)12332-x
De Rycke M., Epigenetic risks related to assisted reproductive technologies: Risk analysis and epigenetic inheritance, 10.1093/humrep/17.10.2487
Shi W., Haaf T., Aberrant methylation patterns at the two-cell stage as an indicator of early developmental failure, 10.1002/mrd.90016
Cox Gerald F., Bürger Joachim, Lip Va, Mau Ulrike A., Sperling Karl, Wu Bai-Lin, Horsthemke Bernhard, Intracytoplasmic Sperm Injection May Increase the Risk of Imprinting Defects, 10.1086/341096
Ørstavik K.H., Eiklid K., van der Hagen C.B., Spetalen S., Kierulf K., Skjeldal O., Buiting K., Another Case of Imprinting Defect in a Girl with Angelman Syndrome Who Was Conceived by Intracytoplasmic Sperm Injection, 10.1086/346030
DeBaun Michael R., Niemitz Emily L., Feinberg Andrew P., Association of In Vitro Fertilization with Beckwith-Wiedemann Syndrome and Epigenetic Alterations of LIT1 and H19, 10.1086/346031
Maher E R, Beckwith-Wiedemann syndrome and assisted reproduction technology (ART), 10.1136/jmg.40.1.62
Gicquel Christine, Gaston Véronique, Mandelbaum Jacqueline, Siffroi Jean-Pierre, Flahault Antoine, Le Bouc Yves, In Vitro Fertilization May Increase the Risk of Beckwith-Wiedemann Syndrome Related to the Abnormal Imprinting of the KCNQ1OT Gene, 10.1086/374824
Halliday Jane, Oke Kay, Breheny Sue, Algar Elizabeth, J. Amor David, Beckwith-Wiedemann Syndrome and IVF: A Case-Control Study, 10.1086/423902
Winston Robert M.L., Hardy Kate, Are we ignoring potential dangers of in vitro fertilization and related treatments?, 10.1038/ncb-nm-fertilitys14
Lucifero D., Potential significance of genomic imprinting defects for reproduction and assisted reproductive technology, 10.1093/humupd/dmh002
Dumoulin John C.M., Derhaag Josien G., Bras Marijke, Van Montfoort Aafke P.A., Kester Arnold D.M., Evers Johannes L.H., Geraedts Joep P.M., Coonen Edith, Growth rate of human preimplantation embryos is sex dependent after ICSI but not after IVF, 10.1093/humrep/deh614
Ponjaert-Kristoffersen I., Tjus T., Nekkebroeck J., Squires J., Verté D., Heimann M., Bonduelle M., Palermo G., Wennerholm U.-B., Psychological follow-up study of 5-year-old ICSI children, 10.1093/humrep/deh511
Vandervorst M., The Brussels' experience of more than 5 years of clinical preimplantation genetic diagnosis, 10.1093/humupd/6.4.364
Iwarsson E., Lundqvist Monalill, Inzunza José, Ährlund-Richter Lars, Sjöblom Peter, Lundkvist Örjan, Simberg Niklas, Nordenskjöld Magnus, Blennow Elisabeth, A high degree of aneuploidy in frozen-thawed human preimplantation embryos, 10.1007/s004390050971
Boiso I., Marti M., Santalo J., Ponsa M., Barri P. N., Veiga A., A confocal microscopy analysis of the spindle and chromosome configurations of human oocytes cryopreserved at the germinal vesicle and metaphase II stage, 10.1093/humrep/17.7.1885
Chen S.U., Lien Y.R., Chao K.H., Ho H.N., Yang Y.S., Lee T.Y., Effects of cryopreservation on meiotic spindles of oocytes and its dynamics after thawing: clinical implications in oocyte freezing—a review article, 10.1016/s0303-7207(03)00070-4
Chian Ri-Cheng, Buckett William M., Jalil Ahmad Kamal Abdul, Son Weon-Young, Sylvestre Camille, Rao Durga, Tan Seang Lin, Natural-cycle in vitro fertilization combined with in vitro maturation of immature oocytes is a potential approach in infertility treatment, 10.1016/j.fertnstert.2004.04.060
Cohen Jacques, Scott Richard, Schimmel Tim, Levron Jacob, Willadsen Steen, Birth of infant after transfer of anucleate donor oocyte cytoplasm into recipient eggs, 10.1016/s0140-6736(05)62353-7
Barritt Jason A., Willadsen Steen, Brenner Carol, Cohen Jacques, Cytoplasmic transfer in assisted reproduction, 10.1093/humupd/7.4.428
Bonduelle M., Liebaers I., Deketelaere V., Derde M.-P., Camus M., Devroey P., Van Steirteghem A., Neonatal data on a cohort of 2889 infants born after ICSI (1991-1999) and of 2995 infants born after IVF (1983-1999), 10.1093/humrep/17.3.671
Bonduelle M, RBM Online, 9, 91 (2004)
Bonduelle M., Developmental outcome at 2 years of age for children born after ICSI compared with children born after IVF, 10.1093/humrep/deg061
Hardy K, Wright C, Rice S, Tachataki M, Roberts R, Morgan D, Spanos S, Taylor D, Future developments in assisted reproduction in humans, 10.1530/rep.0.1230171
Kanavakis E, Preimplantation genetic diagnosis in clinical practice, 10.1136/jmg.39.1.6
Ola Bolarinde, Afnan Masoud, Sharif Khaldoun, Papaioannou Spyros, Hammadieh Nahed, L.R.Barratt Christopher, Should ICSI be the treatment of choice for all cases of in-vitro conception?, 10.1093/humrep/16.12.2485
van Montfoort Aafke P.A., Dumoulin John C.M., Land Jolande A., Coonen Edith, Derhaag Josien G., Evers Johannes L.H., Elective single embryo transfer (eSET) policy in the first three IVF/ICSI treatment cycles, 10.1093/humrep/deh619
De Wert G, Hum Reprod, 18, 672 (2003)
Pennings Guido, Personal desires of patients and social obligations of geneticists: applying preimplantation genetic diagnosis for non-medical sex selection, 10.1002/pd.499
Nys H, Eur J Health Law, 8, 317 (2001)
Turone F., New law forces Italian couple with genetic disease to implant all their IVF embryos, 10.1136/bmj.328.7452.1334-a
Pembrey Marcus E, In the light of preimplantation genetic diagnosis: some ethical issues in medical genetics revisited, 10.1038/sj.ejhg.5200159
Savulescu Julian, Procreative Beneficence: Why We Should Select the Best Children, 10.1111/1467-8519.00251
Boyle R. J, Savulescu J., Ethics of using preimplantation genetic diagnosis to select a stem cell donor for an existing person, 10.1136/bmj.323.7323.1240
Fertil Steril, 82, 773 (2004)
Fertil Steril, 82, 564 (2004)
Golombok S., Brewaeys A., Giavazzi M.T., Guerra D., MacCallum F., Rust J., The European study of assisted reproduction families: the transition to adolescence, 10.1093/humrep/17.3.830
Koropatnick Stephanie, Daniluk Judith, Pattinson H. Anthony, Infertility: a non-event transition, 10.1016/s0015-0282(16)55633-7
Robertson J A, Extending preimplantation genetic diagnosis: medical and non-medical uses, 10.1136/jme.29.4.213
Robertson J. A., Extending preimplantation genetic diagnosis: the ethical debate: Ethical issues in new uses of preimplantation genetic diagnosis, 10.1093/humrep/deg100
Klonoff-Cohen H., Female and male lifestyle habits and IVF: what is known and unknown, 10.1093/humupd/dmh059
Kovacs GT, Med J Aust, 178, 127 (2003)
Robertson J. A., Protecting embryos and burdening women: assisted reproduction in Italy, 10.1093/humrep/deh326
Schenker JG, RBM (online), 10, 310 (2005)
Zlotogora Joël, Parental decisions to abort or continue a pregnancy with an abnormal finding after an invasive prenatal test, 10.1002/pd.472
Bibliographic reference
Soini, S ; Ibarreta, D ; Anastasiadou, V ; Ayme, S ; Braga, S ; et. al. The interface between assisted reproductive technologies and genetics: technical, social, ethical and legal issues. In: European Journal of Human Genetics, Vol. 14, no. 5, p. 588-645 (2006)