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D H Ledbetter

Showing results (161-170 of 251) with videos related to

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European Journal of Human Genetics : EJHG|November 28, 2000
Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndromeN Matsumoto, D E David, E W Johnson, et al.
Pediatric Research|December 14, 1999
Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasiaR P Spiro, S L Christian, D H Ledbetter, et al.
American Journal of Medical Genetics|April 17, 2001
Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African AfrikanersI Simonic, D R Nyholt, G S Gericke, et al.
Genome Research|June 1, 1997
Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human regionS Hirotsune, S D Pack, S S Chong, et al.
American Journal of Human Genetics|September 1, 1993
Nondisjunction of chromosome 15: origin and recombinationW P Robinson, F Bernasconi, A Mutirangura, et al.
Human Molecular Genetics|August 11, 1999
Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1D T Pilz, J Kuc, N Matsumoto, et al.
American Journal of Human Genetics|April 1, 1990
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17P I Patel, B Franco, C Garcia, et al.
American Journal of Ophthalmology|September 1, 1982
Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndromeH M Hittner, R A King, V M Riccardi, et al.
Prenatal Diagnosis|November 1, 1996
Prenatal diagnosis of an infant with mosaic trisomy 16 of paternal originK J Paulyson, D M Sherer, S L Christian, et al.
American Journal of Human Genetics|August 1, 1995
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombinationJ L Blouin, D H Christie, A Gos, et al.
Pageof 26

Showing results (161-170 of 251) with videos related to

Sort By:
Pageof 26
European Journal of Human Genetics : EJHG|November 28, 2000
Breakpoint sequences of an 1;8 translocation in a family with Gilles de la Tourette syndromeN Matsumoto, D E David, E W Johnson, et al.
Pediatric Research|December 14, 1999
Intrauterine growth retardation associated with maternal uniparental disomy for chromosome 6 unmasked by congenital adrenal hyperplasiaR P Spiro, S L Christian, D H Ledbetter, et al.
American Journal of Medical Genetics|April 17, 2001
Further evidence for linkage of Gilles de la Tourette syndrome (GTS) susceptibility loci on chromosomes 2p11, 8q22 and 11q23-24 in South African AfrikanersI Simonic, D R Nyholt, G S Gericke, et al.
Genome Research|June 1, 1997
Genomic organization of the murine Miller-Dieker/lissencephaly region: conservation of linkage with the human regionS Hirotsune, S D Pack, S S Chong, et al.
American Journal of Human Genetics|September 1, 1993
Nondisjunction of chromosome 15: origin and recombinationW P Robinson, F Bernasconi, A Mutirangura, et al.
Human Molecular Genetics|August 11, 1999
Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1D T Pilz, J Kuc, N Matsumoto, et al.
American Journal of Human Genetics|April 1, 1990
Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: identification of new linked markers on chromosome 17P I Patel, B Franco, C Garcia, et al.
American Journal of Ophthalmology|September 1, 1982
Oculocutaneous albinoidism as a manifestation of reduced neural crest derivatives in the Prader-Willi syndromeH M Hittner, R A King, V M Riccardi, et al.
Prenatal Diagnosis|November 1, 1996
Prenatal diagnosis of an infant with mosaic trisomy 16 of paternal originK J Paulyson, D M Sherer, S L Christian, et al.
American Journal of Human Genetics|August 1, 1995
A new dinucleotide repeat polymorphism at the telomere of chromosome 21q reveals a significant difference between male and female rates of recombinationJ L Blouin, D H Christie, A Gos, et al.
Pageof 26