PMC Links for OMIM (Select 305450) - PMC - NCBI

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Items: 6

Select item 41130331.

FG syndrome, an X-linked multiple congenital anomaly syndrome: The clinical phenotype and an algorithm for diagnostic testing

Robin Dawn Clark, John M. Graham, Jr., Michael J. Friez, Joe J. Hoo, Kenneth Lyons Jones, Carole McKeown, John B. Moeschler, F. Lucy Raymond, R. Curtis Rogers, Charles E. Schwartz, Agatino Battaglia, Michael J. Lyons, Roger E. Stevenson

Genet Med. Author manuscript; available in PMC 2014 Jul 28.

Published in final edited form as: Genet Med. 2009 Nov; 11(11): 769–775. doi: 10.1097/GIM.0b013e3181bd3d90

PMCID:: PMC4113033

Abstract Article PDF–214K

Select item 30926002.

Behavior of 10 patients with FG Syndrome (Opitz-Kaveggia Syndrome) and the p.R961W Mutation in the MED12 Gene

John M Graham, Jr, Jeannie Visootsak, Elisabeth Dykens, Lillie Huddleston, Robin D Clark, Kenneth L Jones, John B Moeschler, John M Opitz, Jackie Morford, Richard Simensen, R. Curtis Rogers, Charles E Schwartz, Michael J Friez, Roger E Stevenson

Am J Med Genet A. Author manuscript; available in PMC 2011 May 11.

Published in final edited form as: Am J Med Genet A. 2008 Dec 1; 146A(23): 3011–3017. doi: 10.1002/ajmg.a.32553

PMCID:: PMC3092600

Abstract Article PDF–216K

Select item 10499453.

E Thompson, M Baraitser

J Med Genet. 1987 Mar; 24(3): 139–143. doi: 10.1136/jmg.24.3.139

PMCID:: PMC1049945

Summary Page Browse PDF–1.3M

Select item 10497154.

Necropsy findings in a child with FG syndrome.

E M Thompson, B N Harding, B D Lake, S C Smith

J Med Genet. 1986 Aug; 23(4): 372–373. doi: 10.1136/jmg.23.4.372

PMCID:: PMC1049715

Summary Page Browse PDF–336K

Select item 10490075.

Two retarded male cousins with odd facies, hypotonia, and severe constipation: possible examples of the X linked FG syndrome

J Burn, N Martin

J Med Genet. 1983 Apr; 20(2): 97–99. doi: 10.1136/jmg.20.2.97

PMCID:: PMC1049007

Summary Page Browse PDF–718K

Select item 10156216.

X linked mental retardation: a family with a separate syndrome?

E M Thompson, A Gordon, M Baraitser

J Med Genet. 1989 Jun; 26(6): 373–378. doi: 10.1136/jmg.26.6.373

PMCID:: PMC1015621

Summary Page Browse PDF–904K

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