Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Faivre, L, Cormier-Daire, V, Lapierre, J, Colleaux, L, Jacquemont, S, Genevieve, D, Saunier, P, Munnich, A, Turleau, C, Romana, S, Prieur, M, De Blois, M C, Vekemans, M
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: BMJ Group 2002
Pynciau:
Letter to JMG
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC1735217/
https://ncbi.nlm.nih.gov/pubmed/12161602
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.39.8.594
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