Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation-Reference-Cited by-同舟云学术

Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation

Published:2006 Issue:5 Volume:140A Page:442-452
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Stankiewicz Paweł,Kuechler Alma,Eller C. Daniel,Sahoo Trilochan,Baldermann Christiane,Lieser Ulla,Hesse Martin,Gläser Christiane,Hagemann Monika,Yatsenko Svetlana A.,Liehr Thomas,Horsthemke Bernhard,Claussen Uwe,Marahrens York,Lupski James R.,Hansmann Ingo

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference59 articles.

1. Distal 5q trisomy resulting from an X;5 translocation detected by chromosome painting

2. High concentrations of long interspersed nuclear element sequence distinguish monoallelically expressed genes

3. Trisomy 16q in a female newborn with a de novo X;16 translocation and hypoplastic left heart

4. Molecular evidence for a relationship between LINE-1 elements and X chromosome inactivation: The Lyon repeat hypothesis

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