Bohring–Opitz syndrome (BOS) with a new ASXL1 pathogenic variant: Review of the most prevalent molecular and phenotypic features of the syndrome

Publisher: John Wiley & Sons Inc

E-ISSN: 1552-4833|167|12|3161-3166

ISSN: 1552-4825

Source: American Journal Of Medical Genetics Part A, Vol.167, Iss.12, 2015-12, pp. : 3161-3166

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Abstract