Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny.

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Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny.

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Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny.

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Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny.

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Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny.

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Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny.

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Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny.

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Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny.

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P1476

Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny

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P2093

Asmat Ullah

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

Muhammad Umair

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

Shaheen Shahzad

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

Umm E-Kalsoom

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P2860

ALX4 dysfunction disrupts craniofacial and epidermal development

Fast and accurate short read alignment with Burrows-Wheeler transform

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

The homeoprotein Alx3 contains discrete functional domains and exhibits cell-specific and selective monomeric binding and transactivation.

Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia

Frontonasal dysplasia.

Frontorhiny, a distinctive presentation of frontonasal dysplasia caused by recessive mutations in the ALX3 homeobox gene.

Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology.

Evolution of the Alx homeobox gene family: parallel retention and independent loss of the vertebrate Alx3 gene.

Frontonasal malformation as a field defect and in syndromic associations.

P2888

s10038-017-0358-y

P304

97-100

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P31

scholarly article

P356

10.1038/S10038-017-0358-Y

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P433

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

P478

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P50

Sulman Basit

Wasim Ahmad

P577

2017-11-16T00:00:00Z

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P698

29215096

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