An accessory marker derived from chromosome 20 and its co-existence with a mosaic trisomy 20 cell line
Author:
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Reference18 articles.
1. Follow-up of infants with amniotic fluid trisomy 20 mosaicism
2. Forty four probands with an additional ?marker? chromosome
3. Molecular cytogenetic and clinical studies of 42 patients with marker chromosomes
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1. Mosaicism in rare disease;Genomics of Rare Diseases;2021
2. A systematic analysis of small supernumerary marker chromosomes using array CGH exposes unexpected complexity;Genetics in Medicine;2013-01
3. Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization;Molecular Medicine Reports;2010-09-10
4. Chromosomal breakpoints characterization of two supernumerary ring chromosomes 20;American Journal of Medical Genetics Part A;2010-02
5. Contribution of array CGH in prognosis and genetic counselling of prenatally diagnosed supernumerary ring chromosome 20;Prenatal Diagnosis;2009-08-10
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