Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies-Reference-Cited by-同舟云学术

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Identification of a small supernumerary ring chromosome 8 by fluorescent in situ hybridization in a child with developmental delay and minor anomalies

Published:1994-03-01 Issue:1 Volume:50 Page:12-14
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Melnyk A. R.,Dewald G.

Publisher

Wiley

Subject

Genetics(clinical)

Reference10 articles.

1. (1984): “Clinical Atlas of Human Chromosomes.” 2nd ed. New York: John Wiley and Sons, pp 126-133.

2. Complete and partial trisomy of different segments of chromosome 8: case reports and review

3. Trisomy 8 Mosaicism Syndrome

Cited by 26 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. First case of two supernumerary markers derived from chromosome 5 and chromosome 8;Molecular Cytogenetics;2022-06-27

2. Genomic characterization of chromosome 8 pericentric trisomy;Clinical Case Reports;2015-05-20

3. Molecular cytogenetic and clinical findings in a patient with a small supernumerary r(8) mosaicism;American Journal of Medical Genetics Part A;2007

4. Characterization of two supernumerary marker chromosomes in a patient with signs of Klinefelter syndrome, mild facial anomalies, and severe speech delay;American Journal of Medical Genetics Part A;2006

5. Small supernumerary marker chromosomes – progress towards a genotype-phenotype correlation;Cytogenetic and Genome Research;2005-11-03

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