Multiple congenital anomalies/mental retardation (MCA/MR) syndrome due to interstitial deletion 1q
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference10 articles.
1. Identification of human chromosomes by DNA-binding fluorescent agents
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3. PRIMARY HYPOTHYROIDISM, GROWTH HORMONE DEFICIENCY AND CONGENITAL MALFORMATIONS IN A CHILD WITH THE KARYOTYPE 46, XY, del(l)(q25q32)
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2. Infantile hypertrophic pyloric stenosis—genetics and syndromes;Nature Reviews Gastroenterology & Hepatology;2012-07-10
3. De novo Deletion of 1q31.1q32.1 in a Patient with Developmental Delay and Behavioral Disorders;Cytogenetic and Genome Research;2012
4. Molecular characterization of a patient with an interstitial 1q deletion [del(1)(q24.1q25.3)] and distinctive skeletal abnormalities;American Journal of Medical Genetics Part A;2008-11-15
5. Prenatal diagnosis and molecular characterization of an interstitial 1q24.2q25.2 deletion;European Journal of Medical Genetics;2006-11
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