Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes-Reference-Cited by-同舟云学术

Frequent occurrence of translocations of the short arm of chromosome 15 to other D-group chromosomes

Published:1991-01 Issue:1 Volume:87 Page:45-48
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Smeets Dominique F. C. M.,Merkx Gerard F. M.,Hopman Anton H. M.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF01213090.pdf

Reference13 articles.

1. Babu KA, Verma RS (1984) Fluorescent staining of heterochromatic regions of human chromosomes 1, 9, 15, 16 and the Y by DA/DAPI and D287/170 techniques. Karyogram 10:28?30

2. Babu KA, Macera MJ, Verma RS (1986) Intensity heteromorphisms of human chromosome 15p by DA/DAPI technique. Hum Genet 73:298?300

3. Bross K, Krone W (1973) Ribosomal cistrons and acrocentric chromosomes in man. Humangenetik 18:71?75

4. Bühler EM, Malik NJ (1988) DA/DAPI heteromorphisms in acrocentric chromosomes other than 15. Cytogenet Cell Genet 47:104?105

5. Emmerich P, Loos P, Jauch A, Hopman AHN, Wiegant J, Higgins MJ, White BN, Ploeg M van der, Cremer C, Cremer T (1989) Double in situ hybridization in combination with digital image analysis: a new approach to study interphase chromosome topography. Exp Cell Res 181:126?140

Cited by 27 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. A 25-year odyssey of genomic technology advances and structural variant discovery;Cell;2024-02

2. Resolution of ring chromosomes, Robertsonian translocations, and complex structural variants from long-read sequencing and telomere-to-telomere assembly;2023-09-08

3. Chromosome Variation Detected by Fluorescent In Situ Hybridization (FISH);Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017

4. Chromosome Heteromorphism (Summaries);Human Chromosome Variation: Heteromorphism, Polymorphism and Pathogenesis;2017

5. References;Benign & Pathological Chromosomal Imbalances;2014