Exome sequencing revealed a novel splice site variant in the ALX1 gene underlying frontonasal dysplasia.

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Frontonasal Dysplasia: Towards an Understanding of Molecular and Developmental Aetiology.Exome sequencing revealed a novel nonsense variant in ALX3 gene underlying frontorhiny.

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Exome sequencing revealed a novel splice site variant in the ALX1 gene underlying frontonasal dysplasia.

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2016 nî lūn-bûn

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Exome sequencing revealed a no ...... erlying frontonasal dysplasia.

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Exome sequencing revealed a no ...... erlying frontonasal dysplasia.

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Exome sequencing revealed a no ...... erlying frontonasal dysplasia.

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Exome sequencing revealed a no ...... erlying frontonasal dysplasia.

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Exome sequencing revealed a no ...... erlying frontonasal dysplasia.

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Exome sequencing revealed a no ...... erlying frontonasal dysplasia.

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Exome sequencing revealed a no ...... erlying frontonasal dysplasia.

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

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

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

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.

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scholarly article

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10.1111/CGE.12822

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Exome sequencing revealed a novel splice site variant in the ALX1 gene underlying frontonasal dysplasia.

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P2860

P2860

Exome sequencing revealed a novel splice site variant in the ALX1 gene underlying frontonasal dysplasia.

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