Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4
Author:
Funder
National Science Council
Mackay Memorial Hospital
Publisher
Elsevier BV
Subject
Obstetrics and Gynaecology
Reference30 articles.
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3. Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics;Liehr;Methods Mol Biol,2008
4. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21;Chen;Taiwan J Obstet Gynecol,2010
5. Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22;Chen;Taiwan J Obstet Gynecol,2010
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1. Phenotype to genotype characterization by array-comparative genomic hydridization (a-CGH) in case of fetal malformations: A systematic review;Taiwanese Journal of Obstetrics and Gynecology;2019-01
2. Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q (4q11.1–q13.2) and 5q13.2 microdeletion with no apparent phenotypic abnormality;Taiwanese Journal of Obstetrics and Gynecology;2017-04
3. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15;Taiwanese Journal of Obstetrics and Gynecology;2014-03
4. Mosaic small supernumerary marker chromosome 1 at amniocentesis: Prenatal diagnosis, molecular genetic analysis and literature review;Gene;2013-10
5. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome;Gene;2013-09
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