Clinical and behavioral characteristics in FG syndrome
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference27 articles.
1. 1991. Manual for the child behavior checklist/4-18 and 1991 profile. Burlington, VT: University of Vermont Department of Psychiatry.
2. FG syndrome in a premature male
3. A gene for FG syndrome maps in the Xq12-q21.31 region
4. Two retarded male cousins with odd facies, hypotonia, and severe constipation: possible examples of the X linked FG syndrome
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1. Prenatal diagnosis in a fetuses with a clenched hands, overlapping fingers, and clubfoot due to MED12 deficiency in three affected siblings: A case report;Frontiers in Genetics;2023-07-12
2. Missense MED12 variants in 22 males with intellectual disability: From nonspecific symptoms to complete syndromes;American Journal of Medical Genetics Part A;2022-10-22
3. Microcephaly, disproportionate pontine, and cerebellar hypoplasia syndrome: Two novel mutations in the CASK gene were discovered in Chinese females;International Journal of Developmental Neuroscience;2021-03-05
4. Proteome dynamics during postnatal mouse corpus callosum development;Scientific Reports;2017-03-28
5. A de novo splice site mutation inCASKcauses FG syndrome-4 and congenital nystagmus;American Journal of Medical Genetics Part A;2017-01-31
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