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European Heart Journal
|
September 23, 2011
Aortopulmonary window
Andreas M E Koch, Gerhard Hammersen, André Rüffer
Acta Paediatrica (Oslo, Norway : 1992)
|
December 14, 2007
Varicella-related deaths in children and adolescents--Germany 2003-2004
Veit Grote, Rüdiger von Kries, Wolfgang Springer, et al.
American Journal of Human Genetics
|
February 3, 2007
A defect in dolichol phosphate biosynthesis causes a new inherited disorder with death in early infancy
Christian Kranz, Christoph Jungeblut, Jonas Denecke, et al.
Clinical Endocrinology
|
June 8, 2011
Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey
Friedhelm Raue, Josef Pichl, Helmuth-G Dörr, et al.
American Journal of Human Genetics
|
February 3, 2007
Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation
Francesca Pasutto, Heinrich Sticht, Gerhard Hammersen, et al.
Nature Genetics
|
August 20, 2008
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia
Birgit S Budde, Yasmin Namavar, Peter G Barth, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 6) with videos related to
Sort By:
Page
of 1
European Heart Journal
|
September 23, 2011
Aortopulmonary window
Andreas M E Koch, Gerhard Hammersen, André Rüffer
Acta Paediatrica (Oslo, Norway : 1992)
|
December 14, 2007
Varicella-related deaths in children and adolescents--Germany 2003-2004
Veit Grote, Rüdiger von Kries, Wolfgang Springer, et al.
American Journal of Human Genetics
|
February 3, 2007
A defect in dolichol phosphate biosynthesis causes a new inherited disorder with death in early infancy
Christian Kranz, Christoph Jungeblut, Jonas Denecke, et al.
Clinical Endocrinology
|
June 8, 2011
Activating mutations in the calcium-sensing receptor: genetic and clinical spectrum in 25 patients with autosomal dominant hypocalcaemia - a German survey
Friedhelm Raue, Josef Pichl, Helmuth-G Dörr, et al.
American Journal of Human Genetics
|
February 3, 2007
Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation
Francesca Pasutto, Heinrich Sticht, Gerhard Hammersen, et al.
Nature Genetics
|
August 20, 2008
tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia
Birgit S Budde, Yasmin Namavar, Peter G Barth, et al.
Page
of 1