- ►nih.gov G Piluso, F D'Amico, V Saccone, E Bismuto, … - The American Journal of Human Genetics, 2009 - Elsevier First described in 1974, FG syndrome (FGS) is an X-linked multiple congenital
anomaly/mental retardation (MCA/MR) disorder, characterized by high clinical
variability and genetic heterogeneity. Five loci (FGS1-5) have so far been ... Cited by 1 - Related articles - All 4 versions
[CITATION] Behavior of 10 patients with FG syndrome (Opitz-Kaveggia syndrome) and the p. R961W …
JM Graham Jr. - American Journal of Medical Genetics Part A, 2008 - Wiley Subscription Services, Inc., A Wiley Company … Related articles
M Di Domenico, S Aurino, CE Schwartz, G Neri … - vincenzonigro.it First described in 1974, FG syndrome (FGS) is an X-linked multiple congenital
anomaly/mental retardation (MCA/MR) disorder, char- acterized by high clinical
variability and genetic heterogeneity. Five loci (FGS1-5) have so far been ... Related articles - View as HTML
JM Graham Jr, J Visootsak, E Dykens, L … - American Journal of Medical Genetics Part C: Seminars … - interscience.wiley.com It is also possible that your web browser is not configured or not able to
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[CITATION] Characterization of a new X-linked mental retardation syndrome with microcephaly, cortical …
C du Souich - American Journal of Medical Genetics Part A, 2009 - Wiley Subscription Services, Inc., A Wiley Company …
YP Hsueh, A Sinica - Annals of Neurology, 2009 - interscience.wiley.com Calcium/calmodulin-dependent serine protein kinase (CASK) belongs to the
membrane associated guanylate kinase (MAGUK) protein family. The members of this
protein family function as multiple domain adaptor proteins originally ... Related articles - All 2 versions
[CITATION] Characterization of a New X-Linked Mental Retardation Syndrome With Microcephaly, …