Clinical management of patients with ASXL1 mutations and Bohring–Opitz syndrome, emphasizing the need for Wilms tumor surveillance

Publisher: John Wiley & Sons Inc

E-ISSN: 1552-4833|167|9|2122-2131

ISSN: 1552-4825

Source: American Journal Of Medical Genetics Part A, Vol.167, Iss.9, 2015-09, pp. : 2122-2131

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

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Abstract