ZNF674: A New Krüppel-Associated Box–Containing Zinc-Finger Gene Involved in Nonsyndromic X-Linked Mental Retardation

Array-based comparative genomic hybridization has proven to be successful in the identification of genetic defects in disorders involving mental retardation. Here, we studied a patient with learning disabilities, retinal dystrophy, and short stature. The family history was suggestive of an X-linked...

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Main Authors: Lugtenberg, Dorien, Yntema, Helger G., Banning, Martijn J. G., Oudakker, Astrid R., Firth, Helen V., Willatt, Lionel, Raynaud, Martine, Kleefstra, Tjitske, Fryns, Jean-Pierre, Ropers, Hans-Hilger, Chelly, Jamel, Moraine, Claude, Gécz, Jozef, Reeuwijk, Jeroen van, Nabuurs, Sander B., de Vries, Bert B. A., Hamel, Ben C. J., de Brouwer, Arjan P. M., Bokhoven, Hans van
פורמט: Artigo
שפה:Inglês
יצא לאור: The American Society of Human Genetics 2006
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Articles
גישה מקוונת:https://ncbi.nlm.nih.gov/pmc/articles/PMC1380234/
https://ncbi.nlm.nih.gov/pubmed/16385466
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