Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

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Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

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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

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2015年论文

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2015年论文

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2015年论文

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Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

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Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

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Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

@en

Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

@nl

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Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

@en

Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

@nl

P1476

Microarray Analysis of 8p23.1 Deletion in New Patients with Atypical Phenotypical Traits.

@en

P2093

Ali Saad

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Damien Sanlaville

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Hanene Hannachi

http://www.w3.org/2001/XMLSchema#string

Hatem Elghezal

http://www.w3.org/2001/XMLSchema#string

Hela Ben Khelifa

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Molka Kammoun

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Najla Soyah

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Saber Hammami

http://www.w3.org/2001/XMLSchema#string

Soumaya Mougou-Zerelli

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P2860

Tankyrase, a poly(ADP-ribose) polymerase at human telomeres

Cornelia de Lange syndrome is caused by mutations in NIPBL, the human homolog of Drosophila melanogaster Nipped-B

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

CLDN23 gene, frequently down-regulated in intestinal-type gastric cancer, is a novel member of CLAUDIN gene family

Distal 8p deletion (8p23.1----8pter): a common deletion?

Mutations in microcephalin cause aberrant regulation of chromosome condensation.

Transmitted duplication of 8p23.1-8p23.2 associated with speech delay, autism and learning difficulties

Genomic profile of copy number variants on the short arm of human chromosome 8.

Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1.

Defensins and the dynamic genome: what we can learn from structural variation at human chromosome band 8p23.1.

P304

187-193

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P31

scholarly article

P356

10.1055/S-0035-1565269

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P50

Soumaya Mougou-Zerelli

P577

2015-10-14T00:00:00Z

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P5875

283342927

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P698

27617130

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P932

4906530

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