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Are all Xq26.2 duplications overlapping GPC3 on array-CGH a cause of Simpson-Golabi-Behmel syndrome? When do we need transcript analysis?

Clinical genetics - 1 May 2018

Vuillaume M-L, Moizard M-P, Hammouche E, Delrue M-A, Perrin L, Maftei C, Dupont C, Drunat S, Cottereau E, Baumann C, Toutain A

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Identifiers

PMID: 29372559
DOI: 10.1111/cge.13151

Genes

GPC3

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

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Are all Xq26.2 duplications overlapping GPC3 on array-CGH a cause of Simpson-Golabi-Behmel syndrome? When do we need transcript analysis?PMID 29372559Read ↗

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A 1 Mb-sized microdeletion Xq26.2 encompassing the GPC3 gene in a fetus with Simpson-Golabi-Behmel syndrome Report, antenatal findings and review.Semantic proximity Read ↗

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Prenatal diagnosis of Simpson-Golabi-Behmel syndrome.Semantic proximity Read ↗

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