Reciprocal translocation t(1;15)(p36.2;p11.2): Confirmation of a suggestive cytogenetic diagnosis by in situ hybridization and clinical case report on resulting monosomy (1p)
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Reference12 articles.
1. A 45,X male with molecular evidence of a translocation of Y euchromatin onto chromosome 1
2. A hypervariable repeated sequence on human chromosome 1p36
3. Detection of single-copy genes by nonisotopic in situ hybridization on human chromosomes
4. Relationship between the number and function of human ribosomal genes
5. The CEPH consortium linkage map of human chromosome 1
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1. Recurrence risks for different pregnancy outcomes and meiotic segregation analysis of spermatozoa in carriers of t(1;11)(p36.22;q12.2);Journal of Human Genetics;2014-10-16
2. Complex distal 10q rearrangement in a girl with mild intellectual disability: Follow up of the patient and review of the literature of non-acrocentric satellited chromosomes;American Journal of Medical Genetics Part A;2011-09-30
3. Prenatal diagnosis of monosomy 1p36: A focus on brain abnormalities and a review of the literature;American Journal of Medical Genetics Part A;2008-12-01
4. Complex chromosomal rearrangements associated with congenital erythrophagocytotic histiocytosis;Clinical Genetics;2008-06-28
5. Redundant skin over the nape in a girl with monosomy 1p36 caused by a de-novo satellited derivative chromosome: a possible new feature?;Clinical Dysmorphology;2004-04
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