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D H Ledbetter

Showing results (181-190 of 251) with videos related to

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American Journal of Human Genetics|December 1, 1991
Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4M R Altherr, U Bengtsson, F F Elder, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 1, 1992
Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14M Labuda, T M Fujiwara, M V Ross, et al.
Human Molecular Genetics|February 1, 1994
Olfactory receptor gene cluster on human chromosome 17: possible duplication of an ancestral receptor repertoireN Ben-Arie, D Lancet, C Taylor, et al.
Genes, Chromosomes & Cancer|July 1, 1990
Cloning and characterization of the t(15;17) translocation breakpoint region in acute promyelocytic leukemiaR S Lemons, D Eilender, R A Waldmann, et al.
Clinical Genetics|August 1, 1992
X-linked lymphoproliferative disease: prenatal detection of an unaffected histocompatible maleJ C Mulley, A M Turner, A K Gedeon, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1989
Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sourcesD L Nelson, S A Ledbetter, L Corbo, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 1, 1996
Unilateral cleft lip in a boy with Angelman syndromeO Rösby, P Strömme, M Sandsmark, et al.
American Journal of Medical Genetics|February 13, 1995
Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes"L L Estabrooks, W R Breg, M R Hayden, et al.
Genomics|August 1, 1990
The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocationsP O'Connell, D Viskochil, A M Buchberg, et al.
Genetic Testing|January 1, 1997
Methylation analysis of the fragile X syndrome by PCRS Das, T Kubota, M Song, et al.
Pageof 26

Showing results (181-190 of 251) with videos related to

Sort By:
Pageof 26
American Journal of Human Genetics|December 1, 1991
Molecular confirmation of Wolf-Hirschhorn syndrome with a subtle translocation of chromosome 4M R Altherr, U Bengtsson, F F Elder, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|December 1, 1992
Two hereditary defects related to vitamin D metabolism map to the same region of human chromosome 12q13-14M Labuda, T M Fujiwara, M V Ross, et al.
Human Molecular Genetics|February 1, 1994
Olfactory receptor gene cluster on human chromosome 17: possible duplication of an ancestral receptor repertoireN Ben-Arie, D Lancet, C Taylor, et al.
Genes, Chromosomes & Cancer|July 1, 1990
Cloning and characterization of the t(15;17) translocation breakpoint region in acute promyelocytic leukemiaR S Lemons, D Eilender, R A Waldmann, et al.
Clinical Genetics|August 1, 1992
X-linked lymphoproliferative disease: prenatal detection of an unaffected histocompatible maleJ C Mulley, A M Turner, A K Gedeon, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1989
Alu polymerase chain reaction: a method for rapid isolation of human-specific sequences from complex DNA sourcesD L Nelson, S A Ledbetter, L Corbo, et al.
Journal of Craniofacial Genetics and Developmental Biology|April 1, 1996
Unilateral cleft lip in a boy with Angelman syndromeO Rösby, P Strömme, M Sandsmark, et al.
American Journal of Medical Genetics|February 13, 1995
Summary of the 1993 ASHG ancillary meeting "recent research on chromosome 4p syndromes and genes"L L Estabrooks, W R Breg, M R Hayden, et al.
Genomics|August 1, 1990
The human homolog of murine Evi-2 lies between two von Recklinghausen neurofibromatosis translocationsP O'Connell, D Viskochil, A M Buchberg, et al.
Genetic Testing|January 1, 1997
Methylation analysis of the fragile X syndrome by PCRS Das, T Kubota, M Song, et al.
Pageof 26