Genetic Advances in the Understanding of Microtia.

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Genetic Advances in the Understanding of Microtia.

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2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Genetic Advances in the Understanding of Microtia.

@en

Genetic Advances in the Understanding of Microtia.

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Item

label

Genetic Advances in the Understanding of Microtia.

@en

Genetic Advances in the Understanding of Microtia.

@nl

prefLabel

Genetic Advances in the Understanding of Microtia.

@en

Genetic Advances in the Understanding of Microtia.

@nl

P1476

Genetic Advances in the Understanding of Microtia.

@en

P2093

Ann Schwentker

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

Craig Gendron

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

John A van Aalst

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P2860

Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndrome

SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes

Identification of a primary target of thalidomide teratogenicity

Genomic disorders on 22q11

A mutation in HOXA2 is responsible for autosomal-recessive microtia in an Iranian family.

Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)

A gene locus for branchio-otic syndrome maps to chromosome 14q21.3-q24.3

The mutational spectrum in Treacher Collins syndrome reveals a predominance of mutations that create a premature-termination codon

Transcription factor SIX5 is mutated in patients with branchio-oto-renal syndrome

Branchio-oto-renal syndrome: identification of novel mutations, molecular characterization, mutation distribution, and prospects for genetic testing

P304

189-197

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P31

scholarly article

P356

10.1055/S-0036-1592422

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P433

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

P478

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

P577

2016-09-23T00:00:00Z

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P698

27895971

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P932

5123892

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