Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.

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Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.

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Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.

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Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.

@en

Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.

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Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.

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Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.

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P1476

Congenital diaphragmatic hernia in 22q11.2 deletion syndrome.

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P2093

Elaine H Zackai

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Jessica Barry

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Kathryn Schlechtweg

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Lauren DiCairano

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Lori Howell

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Marta Unolt

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Michael Nance

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N Scott Adzick

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Stefanie Kasperski

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P2860

Role of TBX1 in human del22q11.2 syndrome

DiGeorge syndrome phenotype in mice mutant for the T-box gene, Tbx1

Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies

Tbx1 mutation causes multiple cardiovascular defects and disrupts neural crest and cranial nerve migratory pathways

Decreased embryonic retinoic acid synthesis results in a DiGeorge syndrome phenotype in newborn mice

Prevalence of 22q11 microdeletions in DiGeorge and velocardiofacial syndromes: implications for genetic counselling and prenatal diagnosis

Craniosynostosis and chromosome 22q11 deletion.

Congenital diaphragmatic hernia: a meta-analysis of mortality factors.

Genetic causes of congenital diaphragmatic hernia

Influence of congenital heart disease on survival in children with congenital diaphragmatic hernia.

P304

135-142

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P31

scholarly article

P356

10.1002/AJMG.A.37980

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P407

English

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P478

173

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Donna M McDonald-McGinn

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2016-09-28T00:00:00Z

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P698

27682988

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P921

congenital diaphragmatic hernia