The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey-Reference-Cited by-同舟云学术

The identification of small supernumerary marker chromosomes; the experiences of 15,792 fetal karyotyping from Turkey

Published:2006-05 Issue:3 Volume:49 Page:207-214
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Karaman Birsen,Aytan Melike,Yilmaz Kader,Toksoy Guven,Onal Ebru Perim,Ghanbari Asadollah,Engur Ayse,Kayserili Hulya,Yuksel-Apak Memnune,Basaran Seher

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference36 articles.

1. A non-isotopic in situ hybridisation study of the chromosomal origin of 15 supernumerary marker chromosomes in man;Crolla;J. Med. Genet.,1992

2. Efficient identification of marker chromosomes in 27 patients by stepwise hybridization with alpha-satellite DNA probes;Plattner;Hum. Genet.,1993

3. Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: prevalence and characterization by fluorescence in situ hybridization;Blennow;Prenat. Diagn.,1994

4. Characterization and clinical implications of marker chromosomes identified at prenatal diagnosis;Li;Prenat. Diagn.,2000

5. De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints;Warburton;Am. J. Med. Genet.,1991

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1. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16;Taiwanese Journal of Obstetrics and Gynecology;2017-08

2. Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe;European Journal of Human Genetics;2012-01-11

3. Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances;Journal of Applied Genetics;2011-03-25

4. Multiplex ligation dependent probe amplification (MLPA) for rapid distinction between unique sequence positive and negative marker chromosomes in prenatal diagnosis;Molecular Cytogenetics;2011

5. Detection of Marker Chromosome in the Abortion Material; Does It Reflect the Karyotype of the Pregnancy Lost Tissue or the Maternal Decidual Tissue? Case Report;Turkiye Klinikleri Journal of Medical Sciences;2011