Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12-Reference-Cited by-同舟云学术

Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12

Published:2013-01-29 Issue:3 Volume:97 Page:133-139
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defects Research Part A: Clinical and Molecular Teratology

Author:

Draaken Markus,Mughal Sadaf S.,Pennimpede Tracie,Wolter Stefanie,Wittler Lars,Ebert Anne-Karoline,Rösch Wolfgang,Stein Raimund,Bartels Enrika,Schmidt Dominik,Boemers Thomas M.,Schmiedeke Eberhard,Hoffmann Per,Moebus Susanne,Herrmann Bernhard G.,Nöthen Markus M.,Reutter Heiko,Ludwig Michael

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bdra.23112/fullpdf

Reference32 articles.

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3. Expression analysis of murine genes using in situ hybridization with radioactive and nonradioactively labeled RNA probes;Chotteau-Leliévre;Methods Mol Biol,2006

4. Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy;Draaken;Eur J Med Genet,2010

5. Maternal de novo triple mosaicism for two single OCRL nucleotide substitutions (c.1736A>T, c.1736A>G) in a Lowe syndrome family;Draaken;Hum Genet,2011

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