Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL-Reference-Cited by-同舟云学术

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Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL

Published:2000-12 Issue:12 Volume:8 Page:903-910
ISSN:1018-4813
Container-title:European Journal of Human Genetics
language:en
Short-container-title:Eur J Hum Genet

Author:

Brown Jill,Horsley Sharon W,Jung Christine,Saracoglu Kaan,Janssen Bart,Brough Michaela,Daschner Markus,Beedgen Bernd,Kerkhoffs Guido,Eils Roland,Harris Peter C,Jauch Anna,Kearney Lyndal

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://www.nature.com/articles/5200545.pdf

Cited by 29 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. Molecular combing and its application in clinical settings;Molecular Cytogenetics;2022-11-16

2. Molecular cytogenetics;Cytogenomics;2021

3. Nonmosaic Trisomy 19p13.3p13.2 Resulting from a Rare Unbalanced t(Y;19)(q12;p13.2) Translocation in a Patient with Pachygyria and Polymicrogyria;Cytogenetic and Genome Research;2020

4. Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations;Molecular Cytogenetics;2017-08-04

5. Fluorescence in situ hybridization (FISH);The AGT Cytogenetics Laboratory Manual;2017-03-04

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