Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia.

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Pre- and Postnatal Analysis of Chromosome 15q26.1 and 8p23.1 Deletions in Congenital Diaphragmatic Hernia.

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

@yue

2015年論文

@zh-hant

2015年論文

@zh-hk

2015年論文

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2015年論文

@zh-tw

2015年论文

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2015年论文

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2015年论文

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name

Pre- and Postnatal Analysis of ...... ngenital Diaphragmatic Hernia.

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Pre- and Postnatal Analysis of ...... ngenital Diaphragmatic Hernia.

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type

Item

label

Pre- and Postnatal Analysis of ...... ngenital Diaphragmatic Hernia.

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Pre- and Postnatal Analysis of ...... ngenital Diaphragmatic Hernia.

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prefLabel

Pre- and Postnatal Analysis of ...... ngenital Diaphragmatic Hernia.

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Pre- and Postnatal Analysis of ...... ngenital Diaphragmatic Hernia.

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P1476

Pre- and Postnatal Analysis of ...... ngenital Diaphragmatic Hernia.

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P2093

Jayarama Kadandale

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Mitesh Shetty

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Sridevi Hegde

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P2860

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

Fryns syndrome phenotype caused by chromosome microdeletions at 15q26.2 and 8p23.1

Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia

Molecular pathogenesis of congenital diaphragmatic hernia revealed by exome sequencing, developmental data, and bioinformatics.

Simultaneous visualization of seven different DNA probes by in situ hybridization using combinatorial fluorescence and digital imaging microscopy.

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

Genetic aspects of human congenital diaphragmatic hernia.

Congenital diaphragmatic hernia and chromosome 15q26: determination of a candidate region by use of fluorescent in situ hybridization and array-based comparative genomic hybridization

COUP-TFII gene expression is upregulated in embryonic pleuroperitoneal folds in the nitrofen-induced congenital diaphragmatic hernia rat model.

Prenatal diagnosis of a fetus with ring chromosomal 15 by two- and three-dimensional ultrasonography.

P304

248-253

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scholarly article

P356

10.1159/000442506

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P433

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P478

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2015-12-17T00:00:00Z

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26997946

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P921

congenital diaphragmatic hernia

birth defect

P932

4772715

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