Determining the origins and the structural aberrations of small marker chromosomes in two cases of 45,X/46,X, +mar by use of chromosome-specific DNA probes-Reference-Cited by-同舟云学术

Determining the origins and the structural aberrations of small marker chromosomes in two cases of 45,X/46,X, +mar by use of chromosome-specific DNA probes

Published:1990-09 Issue:1 Volume:37 Page:71-78
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Lin C. C.,Meyne Juliane,Sasi Ramakrishnan,Bowen Peter,Unger T.,Tainaka Tomomi,Hadro Teresa A.,Hoo Joe J.

Publisher

Wiley

Subject

Genetics (clinical)

Reference44 articles.

1. Y chromosome specific probes identify breakpoint in a 45,X/46,X,del(Y)(pter----q11.1:) karyotype of an infertile male.

2. (1985): Clinical and cytologic impact of Y chromosome abnormalities. In (ed) “The Y Chromosome, Part B: Clinical Aspects of Y Chromosome Abnormalities.” New York: Alan R. Liss, pp. 61-93.

3. A mosaic 45,X/46,X,4(?) karyotype investigated with X and Y centromere-specific probes using a non-autoradiographic in situ hybridization technique

4. Identification and characterisation of a small marker chromosome using non-isotopic in situ hybridisation with X and Y specific probes.

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1. Detection of subtle reciprocal translocations by fluorescence in situ hybridization;Clinical Genetics;2008-06-28

2. A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH);Clinical Genetics;2008-06-28

3. Y-derived sequence detected in minute chromosomes by polymerase chain reaction and in situ hybridization;Clinical Genetics;2008-06-28

4. Small supernumerary marker chromosomes (sSMC) in humans;Cytogenetic and Genome Research;2004

5. Phenotype and X inactivation in 45,X/46,X,r(X) cases;American Journal of Medical Genetics;2004