Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivation-Reference-Cited by-同舟云学术

Molecular cytogenetic analysis of a duplication Xp in a female with an abnormal phenotype and random X inactivation

Published:2000-08 Issue:2 Volume:58 Page:116-122
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clinical Genetics

Author:

Portnoï Marie-France,Bouayed-Abdelmoula Nouha,Mirc Myriam,Zemni Ramzi,Castaing Henry,Stephann Julie,Ardalan Azarnouche,Vialard François,Nouchy Marc,Daoud Patrick,Chelly Jamel,Taillemite Jean-Louis

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2000.580205.x/fullpdf

Reference18 articles.

1. Molecular cytogenetic identification of four X chromosome duplications;Zhang;Am J Med Genet,1997

2. Random X-inactivation in a girl with duplication Xp11.21-p21.3: Report of a patient and review of the literature;Matsuo;Am J Med Genet,1999

3. Fluorescence in situ hybridization with human chromosome specific libraries: detection of trisomy 21 and translocations of chromosome 4;Pinkel;Proc Natl Acad Sci USA,1988

4. Probable inverted tamdem duplication of Xp in a 46, Xp+Y boy;Narahara;Jp J Hum Genet,1979

5. Duplication of the X chromosome in males: Evidence that most parts of the X chromosome can be active in two copies;Schmidt;Hum Genet,1991

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