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Characterisation of a microdeletion in Xp11.23 cosegregating in a small family with X-linked retinitis pigmentosa (RP2) and psychosis.
Primary tabs
Document type | Communication à un colloque (Conference Paper) – Abstract, Présentation orale avec comité de sélection |
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Publication date | 2002 |
Language | Anglais |
Conference | "52nd Annual Meeting of the American-Society-of-Human-Genetics", BALTIMORE(Maryland) (Oct 15-19, 2002) |
Journal information | "American Journal of Human Genetics" - Vol. 71, no. 4, p. 508 (2002) |
Peer reviewed | yes |
issn | 0002-9297 |
e-issn | 1537-6605 |
Publisher | Univ Chicago Press (Chicago) |
Affiliation | UCL - Autre |
Links |
Bibliographic reference | Thiselton, DL ; Brandau, O ; Meindl, A ; Riley, BP ; Kendler, KS ; et. al. Characterisation of a microdeletion in Xp11.23 cosegregating in a small family with X-linked retinitis pigmentosa (RP2) and psychosis..52nd Annual Meeting of the American-Society-of-Human-Genetics (BALTIMORE(Maryland), Oct 15-19, 2002). In: American Journal of Human Genetics, Vol. 71, no. 4, p. 508 (2002) |
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Permanent URL | http://hdl.handle.net/2078.1/61594 |