Molecular analysis of a novel intragenic deletion in GPC3 in three cousins with Simpson-Golabi-Behmel syndrome.

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Molecular analysis of a novel intragenic deletion in GPC3 in three cousins with Simpson-Golabi-Behmel syndrome.

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Molecular analysis of a novel ...... impson-Golabi-Behmel syndrome.

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Molecular analysis of a novel ...... impson-Golabi-Behmel syndrome.

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label

Molecular analysis of a novel ...... impson-Golabi-Behmel syndrome.

@en

Molecular analysis of a novel ...... impson-Golabi-Behmel syndrome.

@nl

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Molecular analysis of a novel ...... impson-Golabi-Behmel syndrome.

@en

Molecular analysis of a novel ...... impson-Golabi-Behmel syndrome.

@nl

P1476

Molecular analysis of a novel ...... Simpson-Golabi-Behmel syndrome

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P2093

Frank J Kaiser

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Gabriele Gillessen-Kaesbach

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Ronja Hollstein

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P2860

Mutations in GPC3, a glypican gene, cause the Simpson-Golabi-Behmel overgrowth syndrome

The loss of glypican-3 induces alterations in Wnt signaling

Glypican-3 inhibits Hedgehog signaling during development by competing with patched for Hedgehog binding

Risk of tumorigenesis in overgrowth syndromes: A comprehensive review

Simpson-Golabi-Behmel syndrome types I and II.

Genotype/phenotype correlations of males affected by Simpson-Golabi-Behmel syndrome with GPC3 gene mutations: patient report and review of the literature.

Phenotypic spectrum of Simpson-Golabi-Behmel syndrome in a series of 42 cases with a mutation in GPC3 and review of the literature.

The role of glypican-3 in the regulation of body size and cancer.

Expanding the clinical picture of Simpson-Golabi-Behmel syndrome.

A new X-linked mental retardation-overgrowth syndrome.

P304

1400-1405

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scholarly article

P356

10.1002/AJMG.A.38188

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English

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173

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Julia Schmidt

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2017-03-29T00:00:00Z

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28371070

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