Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.

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Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.

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Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.

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Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.

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Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.

@en

Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.

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Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.

@en

Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.

@nl

P1476

Homozygous sequence variants in the WNT10B gene underlie split hand/foot malformation.

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P2093

Abdul Aziz

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Abdul Wali

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Ajab Gul

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Asmat Ullah

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Farooq Ahmad

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Irfanullah

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Muhammad Umair

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Wasim Ahmad

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P2860

A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly

Wnt signaling: multiple pathways, multiple receptors, and multiple transcription factors

Identification of a novel DLX5 mutation in a family with autosomal recessive split hand and foot malformation

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

Refined mapping of a gene for split hand-split foot malformation (SHFM3) on chromosome 10q25

Split-hand/split-foot malformation is caused by mutations in the p63 gene on 3q27.

Fine mapping of the split-hand/split-foot locus (SHFM3) at 10q24: evidence for anticipation and segregation distortion.

A split hand-split foot (SHFM3) gene is located at 10q24-->25.

Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation.

Pathogenesis of split-hand/split-foot malformation.

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1-8

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scholarly article

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10.1590/1678-4685-GMB-2016-0162

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P433

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P478

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P577

2018-01-22T00:00:00Z

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29384555

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P932

5901503

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