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R Weksberg

Showing results (61-70 of 84) with videos related to

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JAMA|March 9, 1994
Neurodevelopment of children exposed in utero to phenytoin and carbamazepine monotherapyD Scolnik, I Nulman, J Rovet, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 5, 2002
Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndromeA C Smith, J A Squire, P Thorner, et al.
American Journal of Human Genetics|February 1, 1991
A mutation in the pro alpha 2(I) gene (COL1A2) for type I procollagen in Ehlers-Danlos syndrome type VII: evidence suggesting that skipping of exon 6 in RNA splicing may be a common cause of the phenotypeN S Vasan, H Kuivaniemi, B E Vogel, et al.
Journal of Medical Genetics|March 25, 2006
An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene clusterJ B Vincent, S I Horike, S Choufani, et al.
Cytogenetic and Genome Research|April 1, 2006
New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndromeA C Smith, T Rubin, C Shuman, et al.
Placenta|January 24, 2012
A distinct microvascular endothelial gene expression profile in severe IUGR placentasC E Dunk, A M Roggensack, B Cox, et al.
Genes, Chromosomes & Cancer|November 1, 1992
Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombinationM J Coppes, L Bonetta, A Huang, et al.
Journal of Medical Genetics|December 1, 1987
Bridging markers defining the map position of X linked hypophosphataemic ricketsR V Thakker, A P Read, K E Davies, et al.
Human Genetics|December 22, 1999
Alström syndrome: further evidence for linkage to human chromosome 2p13G B Collin, J D Marshall, C F Boerkoel, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
The adult phenotype in Costello syndromeSusan M White, J M Graham, B Kerr, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
JAMA|March 9, 1994
Neurodevelopment of children exposed in utero to phenytoin and carbamazepine monotherapyD Scolnik, I Nulman, J Rovet, et al.
Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 5, 2002
Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndromeA C Smith, J A Squire, P Thorner, et al.
American Journal of Human Genetics|February 1, 1991
A mutation in the pro alpha 2(I) gene (COL1A2) for type I procollagen in Ehlers-Danlos syndrome type VII: evidence suggesting that skipping of exon 6 in RNA splicing may be a common cause of the phenotypeN S Vasan, H Kuivaniemi, B E Vogel, et al.
Journal of Medical Genetics|March 25, 2006
An inversion inv(4)(p12-p15.3) in autistic siblings implicates the 4p GABA receptor gene clusterJ B Vincent, S I Horike, S Choufani, et al.
Cytogenetic and Genome Research|April 1, 2006
New chromosome 11p15 epigenotypes identified in male monozygotic twins with Beckwith-Wiedemann syndromeA C Smith, T Rubin, C Shuman, et al.
Placenta|January 24, 2012
A distinct microvascular endothelial gene expression profile in severe IUGR placentasC E Dunk, A M Roggensack, B Cox, et al.
Genes, Chromosomes & Cancer|November 1, 1992
Loss of heterozygosity mapping in Wilms tumor indicates the involvement of three distinct regions and a limited role for nondisjunction or mitotic recombinationM J Coppes, L Bonetta, A Huang, et al.
Journal of Medical Genetics|December 1, 1987
Bridging markers defining the map position of X linked hypophosphataemic ricketsR V Thakker, A P Read, K E Davies, et al.
Human Genetics|December 22, 1999
Alström syndrome: further evidence for linkage to human chromosome 2p13G B Collin, J D Marshall, C F Boerkoel, et al.
American Journal of Medical Genetics. Part A|June 9, 2005
The adult phenotype in Costello syndromeSusan M White, J M Graham, B Kerr, et al.
Pageof 9