Atypical Williams syndrome in an infant with complete atrioventricular canal defect

E-ISSN： 1552-4833|167|12|3108-3112

ISSN： 1552-4825

Source： American Journal Of Medical Genetics Part A, Vol.167, Iss.12, 2015-12, pp. : 3108-3112

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

Previous Menu Next

Abstract

Related content

A 1.3-Mb 7q11.23 Atypical Deletion Identified in a Cohort of Patients with Williams-Beuren Syndrome

Molecular Syndromology, Vol. 4, Iss. 3, 2013-02 ,pp. : 143-147

Karger

Access to resources Recommend Favorite

Williams–Beuren syndrome: genes and mechanisms

By Francke Uta

Human Molecular Genetics, Vol. 8, Iss. 10, 1999-10 ,pp. : 1947-1954

Oxford University Press

Access to resources Recommend Favorite

Williams–Beuren syndrome: a challenge for genotype–phenotype correlations

By Tassabehji M.

Human Molecular Genetics, Vol. 12, Iss. 2, 2003-10 ,pp. : 229-237

Oxford University Press

Access to resources Recommend Favorite

Atypical presentation of moyamoya disease in an infant with a de novo RNF213 variant

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 11, 2015-11 ,pp. : 2742-2747

John Wiley & Sons Inc

Access to resources Recommend Favorite

Somatic mosaicism in patients with Angelman syndrome and an imprinting defect

By Nazlican Hülya

Human Molecular Genetics, Vol. 13, Iss. 21, 2004-11 ,pp. : 2547-2555

Oxford University Press

Access to resources Recommend Favorite