Characterizing Small Supernumerary Marker Chromosomes with Combination of Multiple Techniques
Author:
Publisher
S. Karger AG
Subject
Genetics(clinical),Genetics,Molecular Biology
Reference32 articles.
1. Mechanisms and Consequences of Small Supernumerary Marker Chromosomes: From Barbara McClintock to Modern Genetic-Counseling Issues
2. Detection of low-level mosaicism by array CGH in routine diagnostic specimens
3. Discovery of a previously unrecognized microdeletion syndrome of 16p11.2–p12.2
4. Partial trisomy of chromosome 22 resulting from a supernumerary marker chromosome 22 in a child with features of cat eye syndrome
5. Molecular cytogenetic characterization of two small supernumerary marker chromosomes derived from chromosome 19
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2. Case Report: Prenatal Identification of a De Novo Mosaic Neocentric Marker Resulting in 13q31.1→qter Tetrasomy in a Mildly Affected Girl;Frontiers in Genetics;2022-07-19
3. Supernumerary derivative 22 chromosome resulting from novel constitutional non-Robertsonian translocation: t(20;22)—Case Report;Molecular Cytogenetics;2022-03-26
4. A Small Supernumerary Xp Marker Chromosome Including Genes NR0B1 and MAGEB Causing Partial Gonadal Dysgenesis and Gonadoblastoma;Sexual Development;2021-09-10
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