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G Stetten

Showing results (51-60 of 63) with videos related to

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American Journal of Human Genetics|January 11, 1992
Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21M J McGinniss, H H Kazazian, G Stetten, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Ring chromosome 21: characterization of DNA sequences at sites of breakage and reunionH H Kazazian, S E Antonarakis, C Wong, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 4, 2000
Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndromeR A Norris, K K Scott, C S Moore, et al.
Neurochemical Research|May 5, 1999
X-linked adrenoleukodystrophy: genes, mutations, and phenotypesK D Smith, S Kemp, L T Braiterman, et al.
Genomics|August 1, 1989
Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21M K McCormick, A Schinzel, M B Petersen, et al.
Human Molecular Genetics|March 11, 1999
Cloning and characterization of a secreted frizzled-related protein that is expressed by the retinal pigment epitheliumJ T Chang, N Esumi, K Moore, et al.
American Journal of Medical Genetics|July 1, 1993
Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21M J McGinniss, C Rosenberg, G Stetten, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1993
The role of the sex-determining region Y gene in the etiology of 46,XX malenessP Y Fechner, S M Marcantonio, V Jaswaney, et al.
Echocardiography (Mount Kisco, N.Y.)|January 12, 2001
Real-time volumetric echocardiography: the technology and the possibilitiesJ Kisslo, B Firek, T Ota, et al.
Journal of Medical Genetics|August 3, 2006
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative studyM D Graf, L Christ, J T Mascarello, et al.
Pageof 7

Showing results (51-60 of 63) with videos related to

Sort By:
Pageof 7
American Journal of Human Genetics|January 11, 1992
Mechanisms of ring chromosome formation in 11 cases of human ring chromosome 21M J McGinniss, H H Kazazian, G Stetten, et al.
Annals of the New York Academy of Sciences|January 1, 1985
Ring chromosome 21: characterization of DNA sequences at sites of breakage and reunionH H Kazazian, S E Antonarakis, C Wong, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|November 4, 2000
Human PRRX1 and PRRX2 genes: cloning, expression, genomic localization, and exclusion as disease genes for Nager syndromeR A Norris, K K Scott, C S Moore, et al.
Neurochemical Research|May 5, 1999
X-linked adrenoleukodystrophy: genes, mutations, and phenotypesK D Smith, S Kemp, L T Braiterman, et al.
Genomics|August 1, 1989
Molecular genetic approach to the characterization of the "Down syndrome region" of chromosome 21M K McCormick, A Schinzel, M B Petersen, et al.
Human Molecular Genetics|March 11, 1999
Cloning and characterization of a secreted frizzled-related protein that is expressed by the retinal pigment epitheliumJ T Chang, N Esumi, K Moore, et al.
American Journal of Medical Genetics|July 1, 1993
Unbalanced translocation, t(18;21), detected by fluorescence in situ hybridization (FISH) in a child with 18q- syndrome and a ring chromosome 21M J McGinniss, C Rosenberg, G Stetten, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1993
The role of the sex-determining region Y gene in the etiology of 46,XX malenessP Y Fechner, S M Marcantonio, V Jaswaney, et al.
Echocardiography (Mount Kisco, N.Y.)|January 12, 2001
Real-time volumetric echocardiography: the technology and the possibilitiesJ Kisslo, B Firek, T Ota, et al.
Journal of Medical Genetics|August 3, 2006
Redefining the risks of prenatally ascertained supernumerary marker chromosomes: a collaborative studyM D Graf, L Christ, J T Mascarello, et al.
Pageof 7