-U Hehr Researcher Activity Profile

Research Author Detailed Information 

U Hehr Publication Rate By Year

U Hehr has published 4 paper(s) in 2004, 2 paper(s) in 2006, for a total of 6 research publications in total.

U U Hehr Author Information

LAST NAME: hehr

FIRST NAME: u

INITIALS: U

AFFILIATION:

Papers

U Hehr's Publication Record

1. Agenesis of the corpus callosum, abnormal genitalia and intractable epilepsy due to a novel familial mutation in the Aristaless-related homeobox gene. Year Published: 2004
Center for Pediatrics and Human Genetics, Hannover Medical School, Hannover, Germany. hartmann.hans@mh-hannover.de
2. X-linked lissencephaly with abnormal genitalia associated with renal phosphate wasting. Year Published: 2004
Department of Neuropediatrics, University of Giessen, Giessen, Germany. Andreas.Hahn@paediat.med.uni-giessen.de
3. Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum. Year Published: 2006
Department of Pediatric Neurology, Hacettepe University, Ankara, Turkey.
4. Agenesis of the corpus callosum, abnormal genitalia and intractable epilepsy due to a novel familial mutation in the Aristaless-related homeobox gene. Year Published: 2004
Center for Pediatrics and Human Genetics, Hannover Medical School, Hannover, Germany. hartmann.hans@mh-hannover.de
5. X-linked lissencephaly with abnormal genitalia associated with renal phosphate wasting. Year Published: 2004
Department of Neuropediatrics, University of Giessen, Giessen, Germany. Andreas.Hahn@paediat.med.uni-giessen.de
6. Further clinical and genetic characterization of SPG11: hereditary spastic paraplegia with thin corpus callosum. Year Published: 2006
Department of Pediatric Neurology, Hacettepe University, Ankara, Turkey.