Brachmann-de Lange syndrome with congenital diaphragmatic hernia and NIPBL gene mutation

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Published in:Congenital Anomalies 2010, Vol.50 (2), p.129-132
Main Authors: Hosokawa, Shinichi, Takahashi, Nobumasa, Kitajima, Hiroyuki, Nakayama, Masahiro, Kosaki, Kenjirou, Okamoto, Nobuhiko
Format: Report
Language:English
Subjects:
Brachmann-de Lange syndrome
congenital diaphragmatic hernia
denaturing high-performance liquid chromatography
direct sequence method
gene mutation
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container_end_page 132
container_issue 2
container_start_page 129
container_title Congenital Anomalies
container_volume 50
creator Hosokawa, Shinichi
Takahashi, Nobumasa
Kitajima, Hiroyuki
Nakayama, Masahiro
Kosaki, Kenjirou
Okamoto, Nobuhiko
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doi_str_mv 10.1111/j.1741-4520.2010.00270.x
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ispartof Congenital Anomalies, 2010, Vol.50 (2), p.129-132
issn 0914-3505
1741-4520
language eng
recordid cdi_istex_primary_ark_67375_WNG_6RX1N2VH_8
source Wiley-Blackwell Read & Publish Collection
subjects Brachmann-de Lange syndrome
congenital diaphragmatic hernia
denaturing high-performance liquid chromatography
direct sequence method
gene mutation
title Brachmann-de Lange syndrome with congenital diaphragmatic hernia and NIPBL gene mutation
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