Author:
Goh Elaine Suk-Ying,Li Chumei,Horsburgh Sheri,Kasai Yumi,Kolomietz Elena,Morel Chantal France
Subject
Genetics(clinical),Genetics
Reference13 articles.
1. History of C-patient with SC-Roberts/Pseudothalidamide syndrome;Feingold;Am J Med Genet,1992
2. The molecular mechanism underlying Roberts syndrome involves loss of ESCO2 acetyltransferase activity;Gordillo;Hum Mol Genet,2008
3. Novel chromosomal aberration in a patient with a unique sleep disorder;Hasegawa;J Neurol Neurosurg Psychiatry,1998
4. A familial dysmorphogenetic syndrome of limb deformities, characteristic facial appearance and associated anomalies: The “pseudothalidomide” or “SC-syndrome.”;Herrmann;Birth defects: Original article series.,1969
5. Roberts/Pseudothalidomide syndrome and normal intelligence: Approaches to diagnosis and management;Holden;Dev Med Child Neurol,1992
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