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M Muenke

Showing results (61-70 of 104) with videos related to

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Nature Genetics|October 15, 1998
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-pairedS A Brown, D Warburton, L Y Brown, et al.
Human Genetics|August 1, 1997
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephalyE Roessler, D E Ward, K Gaudenz, et al.
Human Genetics|December 22, 1999
Structure of the human Lanosterol synthase gene and its analysis as a candidate for holoprosencephaly (HPE1)E Roessler, L Mittaz, Y Du, et al.
Nature Genetics|November 1, 1994
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndromeM Muenke, U Schell, A Hehr, et al.
American Journal of Medical Genetics|August 26, 1998
Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type IIIK W Gripp, C A Stolle, D M McDonald-McGinn, et al.
Nature Genetics|June 16, 1999
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephalyD E Wallis, E Roessler, U Hehr, et al.
Genomics|January 1, 1993
The topographic organization of repetitive DNA in the human nucleolusF S Kaplan, J Murray, J E Sylvester, et al.
American Journal of Human Genetics|May 1, 1993
Molecular analysis of the 18q- syndrome--and correlation with phenotypeA D Kline, M E White, R Wapner, et al.
Molecular Psychiatry|April 20, 2004
Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolateM Arcos-Burgos, F X Castellanos, D Konecki, et al.
Journal of Medical Genetics|February 4, 2005
Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndromeJ S Lee, M Tartaglia, B D Gelb, et al.
Pageof 11

Showing results (61-70 of 104) with videos related to

Sort By:
Pageof 11
Nature Genetics|October 15, 1998
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-pairedS A Brown, D Warburton, L Y Brown, et al.
Human Genetics|August 1, 1997
Cytogenetic rearrangements involving the loss of the Sonic Hedgehog gene at 7q36 cause holoprosencephalyE Roessler, D E Ward, K Gaudenz, et al.
Human Genetics|December 22, 1999
Structure of the human Lanosterol synthase gene and its analysis as a candidate for holoprosencephaly (HPE1)E Roessler, L Mittaz, Y Du, et al.
Nature Genetics|November 1, 1994
A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndromeM Muenke, U Schell, A Hehr, et al.
American Journal of Medical Genetics|August 26, 1998
Phenotype of the fibroblast growth factor receptor 2 Ser351Cys mutation: Pfeiffer syndrome type IIIK W Gripp, C A Stolle, D M McDonald-McGinn, et al.
Nature Genetics|June 16, 1999
Mutations in the homeodomain of the human SIX3 gene cause holoprosencephalyD E Wallis, E Roessler, U Hehr, et al.
Genomics|January 1, 1993
The topographic organization of repetitive DNA in the human nucleolusF S Kaplan, J Murray, J E Sylvester, et al.
American Journal of Human Genetics|May 1, 1993
Molecular analysis of the 18q- syndrome--and correlation with phenotypeA D Kline, M E White, R Wapner, et al.
Molecular Psychiatry|April 20, 2004
Pedigree disequilibrium test (PDT) replicates association and linkage between DRD4 and ADHD in multigenerational and extended pedigrees from a genetic isolateM Arcos-Burgos, F X Castellanos, D Konecki, et al.
Journal of Medical Genetics|February 4, 2005
Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndromeJ S Lee, M Tartaglia, B D Gelb, et al.
Pageof 11