Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: Clinical data and molecular characterization-Reference-Cited by-同舟云学术

Monosomy 19pter and trisomy 19q13-qter in two siblings arising from a maternal pericentric inversion: Clinical data and molecular characterization

Published:2008-11 Issue:6 Volume:51 Page:622-630
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Schluth-Bolard Caroline,Till Marianne,Rafat Azim,Labalme Audrey,Le Lorc'h Marc,Banquart Emmanuelle,Angei Christelle,Cordier Marie-Pierre,Romana Serge-Pierrick,Edery Patrick,Sanlaville Damien

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference15 articles.

1. Distinct phenotype associated with a cryptic subtelomeric deletion of 19p13.3-pter;Archer;Am. J. Med. Genet. A,2005

2. The prenatal detection of a familial pericentric inversion of chromosome 19;Couzin;Prenat. Diagn.,1986

3. Pericentric inversion of chromosome 19 in three families;D'Alessandro;Hum. Genet.,1988

4. Pericentric inversion of chromosome 19;Dallapiccola;Prenat. Diagn.,1986

5. A cytogenetic survey of 14,069 newborn infants. I. Incidence of chromosome abnormalities;Hamerton;Clin. Genet.,1975

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