Refinement of the Region for Split Hand/Foot Malformation 5 on 2q31.1

Publisher： Karger

E-ISSN： 1661-8777|1|5|262-271

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.1, Iss.5, 2011-05, pp. : 262-271

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 new locus for split hand/foot malformation with long bone deficiency (SHFLD) at 2q14.2 identified from a chromosome translocation

By Babbs Christian   Heller Raoul   Everman David   Crocker Mark   Twigg Stephen   Schwartz Charles   Giele Henk   Wilkie Andrew  

Human Genetics, Vol. 122, Iss. 2, 2007-09 ,pp. : 191-199

Springer Publishing Company

Access to resources Recommend Favorite

Split Hand/Foot Malformation Associated with 7q21.3 Microdeletion: A Case Report

By  

Molecular Syndromology, Vol. 6, Iss. 6, 2016-0 ,pp. : 287-296

Karger

Access to resources Recommend Favorite

Characterization of the Split Hand/Split Foot Malformation Locus SHFM1 at 7Q21.3–Q22.1 and Analysis of a Candidate Gene for Its Expression during Limb Development

By Crackower Michael A.  

Human Molecular Genetics, Vol. 5, Iss. 5, 1996-01 ,pp. : 571-579

Oxford University Press

Access to resources Recommend Favorite

Derogatory nomenclature is still being used: The example of split hand/foot

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 4, 2015-04 ,pp. : 928-929

John Wiley & Sons Inc

Access to resources Recommend Favorite

Homozygous WNT10b mutation and complex inheritance in Split-Hand/Foot Malformation

By Ugur Sibel Aylin   Tolun Aslihan  

Human Molecular Genetics, Vol. 17, Iss. 17, 2008-09 ,pp. : 2644-2653

Oxford University Press

Access to resources Recommend Favorite