Unique mosaicism of structural chromosomal rearrangement: Is chromosome 18 preferentially involved?
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference37 articles.
1. 18q− and 18q+ mosaicism in a mentally retarded boy
2. Triple structural mosaicism of chromosome 18 in a child with MR/MCA syndrome and abnormal skin pigmentation.
3. Abnormal Chromosome 18 in prenatal diagnosis with holoprosencephaly
4. Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21
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1. Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report;BMC Medical Genomics;2020-09-24
2. Somatic/gonadal mosaicism for structural autosomal rearrangements: female predominance among carriers of gonadal mosaicism for unbalanced rearrangements;Molecular Cytogenetics;2016-01-28
3. Jacobsen and Beckwith-Wiedemann syndromes in a child with mosaicism for partial 11pter trisomy and partial 11qter monosomy;American Journal of Medical Genetics Part A;2013-01-15
4. Case report of de novo dup(18p)/del(18q) and r(18) mosaicism;Journal of Human Genetics;2008-08-05
5. Cytogenetic investigation of a child with a mosaic isochromosome 18q and ring 18q;European Journal of Medical Genetics;2007-09
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