An additional clinical sign of 17q21.31 microdeletion syndrome: Preaxial polydactyly of hands with broad thumbs

Publisher： John Wiley & Sons Inc

E-ISSN： 1552-4833|167|7|1671-1673

ISSN： 1552-4825

Source： American Journal Of Medical Genetics Part A, Vol.167, Iss.7, 2015-07, pp. : 1671-1673

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

Complex Phenotype Associated with 17q21.31 Microdeletion

By  

Molecular Syndromology, Vol. 4, Iss. 6, 2013-08 ,pp. : 297-301

Karger

Access to resources Recommend Favorite

Recurrent Transmission of a 17q12 Microdeletion and a Variable Clinical Spectrum

By  

Molecular Syndromology, Vol. 2, Iss. 2, 2011-12 ,pp. : 72-75

Karger

Access to resources Recommend Favorite

Clinical and molecular characterization of an emerging chromosome 22q13.31 microdeletion syndrome

By  

American Journal Of Medical Genetics Part A, Vol. 176, Iss. 2, 2018-02 ,pp. : 391-398

John Wiley & Sons Inc

Access to resources Recommend Favorite

Clinical and Genetic Heterogeneity of the 15q13.3 Microdeletion Syndrome

By  

Molecular Syndromology, Vol. 6, Iss. 5, 2015-0 ,pp. : 222-228

Karger

Access to resources Recommend Favorite

Delineation of the clinically recognizable 17q22 contiguous gene deletion syndrome in a patient carrying the smallest microdeletion known to date

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 9, 2015-09 ,pp. : 2034-2041

John Wiley & Sons Inc

Access to resources Recommend Favorite