Robertsonian translocation and an extra microchromosome: independent origin identified by in situ hybridization
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1991.tb02993.x/fullpdf
Reference10 articles.
1. DA/DAPI heteromorphisms in acrocentric chromosomes other than 15;Buhler;Cytogenet. Cell Genet.,1988
2. Isolation of molecular probes associated with chromosome 15 instability in the Prader-Willi syndrome;Donlon;P.N.A.S.,1986
3. Breakage of the T-cell receptor alpha-chain locus in non-malignant clones from patients with ataxia telangiectasia;Heppell;Hum. Genet.,1988
4. Robertsonian translocation and an extra microchromosome: aetiology and effect on meiotic segregation;Howard;Clin. Genet.,1987
5. Evidence of lack of specificity of the DA/DAPI technique;Perez-Castillo;Cytogenet. Cell Genet.,1987
Cited by 7 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 cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10);Taiwanese Journal of Obstetrics and Gynecology;2022-01
2. A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH);Clinical Genetics;2008-06-28
3. Robertsonian translocation and an extra microchromosome: independent origin identified by in situ hybridisation;Clinical Genetics;2008-06-28
4. Reassessment of a chromosome 12q + marker by fluorescent in situ hybridization (FISH);Clinical Genetics;2008-06-28
5. Infertility in carriers of two bisatellited marker chromosomes;Clinical Genetics;2008-04-23
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