FISH and molecular study of autosomal supernumerary marker chromosomes excluding those derived from chromosomes 15 and 22: I. Results of 26 new cases
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference40 articles.
1. Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescencein situ hybridization
2. Fifty probands with extra structurally abnormal chromosomes characterized by fluorescence in situ hybridization
3. A 10-year survey, 1980–1990, of prenatally diagnosed small supernumerary marker chromosomes, identified by fish analysis. Outcome and follow-up of 14 cases diagnosed in a series of 12 699 prenatal samples
4. Forty four probands with an additional ?marker? chromosome
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3. Molecular characterization of small supernumerary marker chromosomes derived from chromosome 14/22 detected in adult women with fertility problems;Medicine;2020-10-02
4. Molecular Cytogenetic Diagnostics of Marker Chromosomes: Analysis in Four Prenatal Cases and Long-Term Clinical Evaluation of Carriers;Cytogenetic and Genome Research;2018
5. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review;Taiwanese Journal of Obstetrics and Gynecology;2017-08
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