Genotypes and Phenotypes of 162 Families with a Glomulin Mutation

Publisher： Karger

E-ISSN： 1661-8777|4|4|157-164

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.4, Iss.4, 2013-03, pp. : 157-164

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

Understanding Genotypes and Phenotypes in Epileptic Encephalopathies

By  

Molecular Syndromology, Vol. 7, Iss. 4, 2016-08 ,pp. : 172-181

Karger

Access to resources Recommend Favorite

Genethics 2.0: Phenotypes, Genotypes, and the Challenge of Databases Generated by Personal Genome Testing

By Esposito Karin   Goodman Kenneth  

American Journal of Bioethics, Vol. 9, Iss. 6-7, 2009-06 ,pp. : 19-21

Routledge Ltd

Access to resources Recommend Favorite

Temperature-sensitive mutation in PEX1 moderates the phenotypes of peroxisome deficiency disorders

By Fujiki Y.  

Human Molecular Genetics, Vol. 7, Iss. 13, 1998-12 ,pp. : 2089-2094

Oxford University Press

Access to resources Recommend Favorite

Polymorphisms of the tumor necrosis factor-alpha receptor 2 gene are associated with obesity phenotypes among 405 Caucasian nuclear families

By Zhao Lan-Juan  

Human Genetics, Vol. 124, Iss. 2, 2008-09 ,pp. : 171-177

Springer Publishing Company

Access to resources Recommend Favorite

Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families

By Bouzigon Emmanuelle  

Human Molecular Genetics, Vol. 13, Iss. 24, 2004-12 ,pp. : 3103-3113

Oxford University Press

Access to resources Recommend Favorite