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K Zerres

Showing results (131-140 of 174) with videos related to

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Clinical Genetics|January 1, 1989
Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneityA Gal, B Wirth, H Kääriäinen, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Intelligence and cognitive function in children and adolescents with spinal muscular atrophyA von Gontard, K Zerres, M Backes, et al.
Molecular Genetics and Metabolism|June 2, 2001
A novel neurodevelopmental syndrome responsive to 5-hydroxytryptophan and carbidopaV T Ramaekers, J Senderek, M Häusler, et al.
Journal of Human Hypertension|July 23, 2003
Relation between the angiotensinogen (AGT) M235T gene polymorphism and blood pressure in a large, homogeneous study populationJ R Ortlepp, J Metrikat, V Mevissen, et al.
Journal of Child Neurology|August 13, 1998
Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophyH Omran, U P Ketelsen, F Heinen, et al.
American Journal of Human Genetics|June 1, 1997
Identification of mutations in the duplicated region of the polycystic kidney disease 1 gene (PKD1) by a novel approachB Peral, V Gamble, C Strong, et al.
Clinical Genetics|September 29, 2009
Genotype-phenotype studies in infantile spinal muscular atrophy (SMA) type I in Germany: implications for clinical trials and genetic counsellingS Rudnik-Schöneborn, C Berg, K Zerres, et al.
Journal of Medical Genetics|July 30, 2008
Congenital heart disease is a feature of severe infantile spinal muscular atrophyS Rudnik-Schöneborn, R Heller, C Berg, et al.
Heart (British Cardiac Society)|April 12, 2006
APOE alleles are not associated with calcific aortic stenosisJ R Ortlepp, M Pillich, V Mevissen, et al.
Human Molecular Genetics|August 1, 1995
Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAsB Wirth, E Hahnen, K Morgan, et al.
Pageof 18

Showing results (131-140 of 174) with videos related to

Sort By:
Pageof 18
Clinical Genetics|January 1, 1989
Childhood manifestation of autosomal dominant polycystic kidney disease: no evidence for genetic heterogeneityA Gal, B Wirth, H Kääriäinen, et al.
Neuromuscular Disorders : NMD|December 12, 2001
Intelligence and cognitive function in children and adolescents with spinal muscular atrophyA von Gontard, K Zerres, M Backes, et al.
Molecular Genetics and Metabolism|June 2, 2001
A novel neurodevelopmental syndrome responsive to 5-hydroxytryptophan and carbidopaV T Ramaekers, J Senderek, M Häusler, et al.
Journal of Human Hypertension|July 23, 2003
Relation between the angiotensinogen (AGT) M235T gene polymorphism and blood pressure in a large, homogeneous study populationJ R Ortlepp, J Metrikat, V Mevissen, et al.
Journal of Child Neurology|August 13, 1998
Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophyH Omran, U P Ketelsen, F Heinen, et al.
American Journal of Human Genetics|June 1, 1997
Identification of mutations in the duplicated region of the polycystic kidney disease 1 gene (PKD1) by a novel approachB Peral, V Gamble, C Strong, et al.
Clinical Genetics|September 29, 2009
Genotype-phenotype studies in infantile spinal muscular atrophy (SMA) type I in Germany: implications for clinical trials and genetic counsellingS Rudnik-Schöneborn, C Berg, K Zerres, et al.
Journal of Medical Genetics|July 30, 2008
Congenital heart disease is a feature of severe infantile spinal muscular atrophyS Rudnik-Schöneborn, R Heller, C Berg, et al.
Heart (British Cardiac Society)|April 12, 2006
APOE alleles are not associated with calcific aortic stenosisJ R Ortlepp, M Pillich, V Mevissen, et al.
Human Molecular Genetics|August 1, 1995
Allelic association and deletions in autosomal recessive proximal spinal muscular atrophy: association of marker genotype with disease severity and candidate cDNAsB Wirth, E Hahnen, K Morgan, et al.
Pageof 18