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Drouin-Garraud, Valérie
Cahill, John B
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Journal article
Novel FOXF1 mutations in sporadic and familial cases of alveolar capillary dysplasia with misaligned pulmonary veins imply a role for its DNA binding domain
Sen, Partha
Yang, Yaping
Navarro, Colby
Silva, Iris
Szafranski, Przemyslaw
Kolodziejska, Katarzyna E
Dharmadhikari, Avinash V
Mostafa, Hasnaa
Kozakewich, Harry
Kearney, Debra
Cahill, John B
Whitt, Merrissa
Bilic, Masha
Margraf, Linda
Charles, Adrian
Goldblatt, Jack
Gibson, Kathleen
Lantz, Patrick E
Garvin, A Julian
Petty, John
Kiblawi, Zeina
Zuppan, Craig
McConkie-Rosell, Allyn
McDonald, Marie T
Peterson-Carmichael, Stacey L
Gaede, Jane T
Shivanna, Binoy
Schady, Deborah
Friedlich, Philippe S
Hays, Stephen R
Palafoll, Irene Valenzuela
Siebers-Renelt, Ulrike
Bohring, Axel
Finn, Laura S
Siebert, Joseph R
Galambos, Csaba
Nguyen, Lananh
Riley, Melissa
Chassaing, Nicolas
Vigouroux, Adeline
Rocha, Gustavo
Fernandes, Susana
Brumbaugh, Jane
Roberts, Kari
Ho-Ming, Luk
Lo, Ivan F M
Lam, Stephen
Gerychova, Romana
Jezova, Marta
Valaskova, Iveta
Fellmann, Florence
Afshar, Katayoun
Giannoni, Eric
Muhlethaler, Vincent
Liang, Jinlong
Beckmann, Jacques S
Lioy, Janet
Deshmukh, Hitesh
Srinivasan, Lakshmi
Swarr, Daniel T
Sloman, Melissa
Shaw-Smith, Charles
van Loon, Rosa Laura
Hagman, Cecilia
Sznajer, Yves
[UCL]
Barréa, Catherine
[UCL]
Galant, Christine
[UCL]
Detaille, Thierry
[UCL]
Wambach, Jennifer A
Cole, F Sessions
Hamvas, Aaron
Prince, Lawrence S
Diderich, Karin E M
Brooks, Alice S
Verdijk, Robert M
Ravindranathan, Hari
Sugo, Ella
Mowat, David
Baker, Michael L
Langston, Claire
Welty, Stephen
Stankiewicz, Pawel
(2013)
Human Mutation — Vol. 34, no. 6, p. 801-811 (2013)