Dup(lq)(q42→qter) syndrome: Case report and review of literature
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference26 articles.
1. Trisomy-18 Mosaicism with Features of Russell-Silver Syndrome
2. DELETION SHORT ARM 18 AND SILVER-RUSSELL SYNDROME
3. Phenotypic and genetic analysis of the Silver-Russell syndrome
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1. Trisomy 1q41-qter and monosomy 3p26.3-pter in a family with a translocation (1;3): further delineation of the syndromes;BMC Medical Genomics;2014-09-15
2. Human imprinting syndromes;Epigenomics;2009-12
3. The genetic aetiology of Silver-Russell syndrome;Journal of Medical Genetics;2007-12-21
4. Trisomy 1q42.3-qter and monosomy 21q22.3-qter associated with ear anomaly, facial dysmorphology, psychomotor retardation, and epilepsy: Delineation of a new syndrome;American Journal of Medical Genetics Part A;2007
5. Calibration of 6q subtelomere deletions to define genotype/phenotype correlations;Clinical Genetics;2005-02-22
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