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K Zerres

Showing results (101-110 of 174) with videos related to

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Journal of the Neurological Sciences|November 10, 2001
Phenotypic variation of a novel nonsense mutation in the P0 intracellular domainJ Senderek, V T Ramaekers, K Zerres, et al.
Developmental Medicine and Child Neurology|January 29, 2003
Behavioural problems in children and adolescents with spinal muscular atrophy and their siblingsC Laufersweiler-Plass, S Rudnik-Schöneborn, K Zerres, et al.
Genomics|January 1, 1993
Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studiesB Wirth, B Voosen, D Röhrig, et al.
American Journal of Human Genetics|December 1, 1993
Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia AJ Oldenburg, R Schwaab, T Grimm, et al.
Zeitschrift Fur Kardiologie|February 1, 1990
[Fetal echocardiography and clinical genetics--a close correlation]K Zerres, U Gembruch, G Schwanitz, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 1, 1996
Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender. Arbeitsgemeinschaft für Pädiatrische, NephrologieK Zerres, S Rudnik-Schöneborn, F Deget, et al.
Human Molecular Genetics|October 1, 1995
Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individualsE Hahnen, R Forkert, C Marke, et al.
Annales De Genetique|May 4, 2001
Origin of uniparental disomy 6: presentation of a new case and review on the literatureT Eggermann, W Marg, S Mergenthaler, et al.
Neuroradiology|January 13, 2005
White-matter disease in 18q deletion (18q-) syndrome: magnetic resonance spectroscopy indicates demyelination or increased myelin turnover rather than dysmyelinationM Häusler, D Anhuf, H Schüler, et al.
Human Genetics|January 1, 1991
No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markersK Kausch, C R Müller, T Grimm, et al.
Pageof 18

Showing results (101-110 of 174) with videos related to

Sort By:
Pageof 18
Journal of the Neurological Sciences|November 10, 2001
Phenotypic variation of a novel nonsense mutation in the P0 intracellular domainJ Senderek, V T Ramaekers, K Zerres, et al.
Developmental Medicine and Child Neurology|January 29, 2003
Behavioural problems in children and adolescents with spinal muscular atrophy and their siblingsC Laufersweiler-Plass, S Rudnik-Schöneborn, K Zerres, et al.
Genomics|January 1, 1993
Fine mapping and narrowing of the genetic interval of the spinal muscular atrophy region by linkage studiesB Wirth, B Voosen, D Röhrig, et al.
American Journal of Human Genetics|December 1, 1993
Direct and indirect estimation of the sex ratio of mutation frequencies in hemophilia AJ Oldenburg, R Schwaab, T Grimm, et al.
Zeitschrift Fur Kardiologie|February 1, 1990
[Fetal echocardiography and clinical genetics--a close correlation]K Zerres, U Gembruch, G Schwanitz, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 1, 1996
Autosomal recessive polycystic kidney disease in 115 children: clinical presentation, course and influence of gender. Arbeitsgemeinschaft für Pädiatrische, NephrologieK Zerres, S Rudnik-Schöneborn, F Deget, et al.
Human Molecular Genetics|October 1, 1995
Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individualsE Hahnen, R Forkert, C Marke, et al.
Annales De Genetique|May 4, 2001
Origin of uniparental disomy 6: presentation of a new case and review on the literatureT Eggermann, W Marg, S Mergenthaler, et al.
Neuroradiology|January 13, 2005
White-matter disease in 18q deletion (18q-) syndrome: magnetic resonance spectroscopy indicates demyelination or increased myelin turnover rather than dysmyelinationM Häusler, D Anhuf, H Schüler, et al.
Human Genetics|January 1, 1991
No evidence for linkage of autosomal dominant proximal spinal muscular atrophies to chromosome 5q markersK Kausch, C R Müller, T Grimm, et al.
Pageof 18