Non C-banding variants in some normal families might be homogeneously staining regions-Reference-Cited by-同舟云学术

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Non C-banding variants in some normal families might be homogeneously staining regions

Published:1989-04 Issue:1 Volume:82 Page:59-62
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Webb Graham C.,Krumins Edgar J. M.,Eichenbaum Sam Z.,Voullaire Lucille E.,Earle Elizabeth,Choo Kong H.

Publisher

Springer Science and Business Media LLC

Subject

Genetics (clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/BF00288273.pdf

Reference21 articles.

1. Archidiacono N, Pecile V, Rocchi M, Dalpra L, Nocera G, Simoni G (1984) A rare non-heterochromatic 9p+ variant in two amniotic cell cultures. Prenat Diagn 4:231?233

2. Barker PE, Lau YF, Hsu TC (1980) A heterochromatic homogeneously staining region (HSR) in the karyotype of a human breast carcinoma cell line. Cancer Genet Cytogenet 1:311?319

3. Biedler JL, Spengler BA (1976) Metaphase chromosome anomaly: association with drug resistance and cell specific products. Science 191:185?187

4. Boldyreff B, Winking H, Weith A, Traut W (1988) Evidence for in situ amplification of a germ line homogeneously staining region in the mouse. Cytogenet Cell Genet 47:84?85

5. Buckle VJ, Craig IW (1986) In situ hybridization. In: Davies KE (ed) Human genetic diseases: a practical approach. IRL Press, Oxford, pp 85?100

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1. Prenatal diagnosis of a familial 9p12 amplification inherited from a father carrier;Taiwanese Journal of Obstetrics and Gynecology;2021-09

2. C-banding and AgNOR-staining were still effective complementary methods to indentify chromosomal heteromorphisms and some structural abnormalities in prenatal diagnosis;Molecular Cytogenetics;2019-09-18

3. Chromosome abnormalities without phenotypic consequences;Journal of Applied Genetics;2007-06

4. The first 4p euchromatic variant in a healthy carrier having an unusual reproductive history;American Journal of Medical Genetics Part A;2007

5. The euchromatic 9p+ polymorphism is a locus-specific amplification caused by repeated copies of a small DNA segment mapping within 9p12;Human Genetics;2005-12-02

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