Mosaic tetrasomy 21 in a male child-Reference-Cited by-同舟云学术

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Mosaic tetrasomy 21 in a male child

Published:2008-04-23 Issue:2 Volume:26 Page:150-155
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Kwee M. L.,Barth P. G.,Arwert F.,Madan K.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1984.tb00805.x/fullpdf

Reference8 articles.

1. Mosaic Tetrasomy 21 in Severe Mental Handicap;Fryns;Eur. J. Pediatr.,1982

2. Hunter , A. G. W. B. Clifford M. Speevak S. Brock MacMurray 1982 Mosaic tetrasomy

3. in a liveborn male infant Clin. Genet. 21 228 232

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1. Abnormally Flat Facial Profile on Two- and Three-dimensional Ultrasound and Array Comparative Genomic Hybridization for the Diagnosis of Pallister-Killian Syndrome;Taiwanese Journal of Obstetrics and Gynecology;2010-03

2. Pallister-Killian syndrome [i(12p)]: first pre-natal diagnosis using cordocentesis in the second trimester confirmed by in situ hybridization;Clinical Genetics;2008-06-28

3. Case Report: Prenatal diagnosis of mosaic tetrasomy 21q confirmed by fluorescence in situ hybridization;Clinical Genetics;2008-06-28

4. Risk effect of maternal age in Pallister i(12p) syndrome;Clinical Genetics;2008-06-28

5. Pallister-Killian syndrome: cytogenetic and molecular studies;Clinical Genetics;2008-06-28

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