Deletion of chromosome 8q22.1, a critical region for Nablus mask‐like facial syndrome: Four additional cases support a role of genetic modifiers in the manifestation of the phenotype

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 6, 2015-06 ,pp. : 1400-1405

John Wiley & Sons Inc

Access to resources Recommend Favorite

Severe CNS involvement in WWOX mutations: Description of five new cases

By  

American Journal Of Medical Genetics Part A, Vol. 167, Iss. 12, 2015-12 ,pp. : 3209-3213

John Wiley & Sons Inc

Access to resources Recommend Favorite

Population description and its role in the interpretation of genetic association

By Fullerton Stephanie   Yu Joon-Ho   Crouch Julia   Fryer-Edwards Kelly   Burke Wylie  

Human Genetics, Vol. 127, Iss. 5, 2010-05 ,pp. : 563-572

Springer Publishing Company

Access to resources Recommend Favorite

Expression analyses and interaction with the anaphase promoting complex protein Apc2 suggest a role for inversin in primary cilia and involvement in the cell cycle

By Goodship J.A.  

Human Molecular Genetics, Vol. 11, Iss. 26, 2002-12 ,pp. : 3345-3350

Oxford University Press

Access to resources Recommend Favorite

A complex pattern of evolutionary conservation and alternative polyadenylation within the long 3"-untranslated region of the methyl-CpG-binding protein 2 gene ( MeCP2 ) suggests a regulatory role in gene expression

By Coy Johannes F.  

Human Molecular Genetics, Vol. 8, Iss. 7, 1999-07 ,pp. : 1253-1262

Oxford University Press

Access to resources Recommend Favorite