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Rivka Carmi

Showing results (11-20 of 21) with videos related to

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Human Immunology|June 1, 2002
HLA DQA1-DQB1 genotypes in Bedouin families with celiac diseaseSusan L Neuhausen, Zvi Weizman, Nicola J Camp, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
Homozygosity mapping of lethal congenital contractural syndrome type 2 (LCCS2) to a 6 cM interval on chromosome 12q13Ginat Narkis, Daniella Landau, Esther Manor, et al.
Investigative Ophthalmology & Visual Science|April 27, 2007
Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataractDavid Cohen, Udy Bar-Yosef, Jaime Levy, et al.
American Journal of Human Genetics|July 20, 2004
Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)Annie P Chiang, Darryl Nishimura, Charles Searby, et al.
Nature Genetics|May 29, 2002
Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemiaRoxanne Y Walder, Daniel Landau, Peter Meyer, et al.
European Journal of Human Genetics : EJHG|August 9, 2007
Population history and infrequent mutations: how old is a rare mutation? GUCY2D as a worked exampleSylvain Hanein, Isabelle Perrault, Sylvie Gerber, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 13, 2004
Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsinDarryl Y Nishimura, Melissa Fath, Robert F Mullins, et al.
Lancet (London, England)|April 7, 2005
Promoting Arab and Israeli cooperation: peacebuilding through health initiativesHarvey Skinner, Ziad Abdeen, Hani Abdeen, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2006
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)Annie P Chiang, John S Beck, Hsan-Jan Yen, et al.
Nature Genetics|July 16, 2002
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndromeKirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Human Immunology|June 1, 2002
HLA DQA1-DQB1 genotypes in Bedouin families with celiac diseaseSusan L Neuhausen, Zvi Weizman, Nicola J Camp, et al.
American Journal of Medical Genetics. Part A|September 21, 2004
Homozygosity mapping of lethal congenital contractural syndrome type 2 (LCCS2) to a 6 cM interval on chromosome 12q13Ginat Narkis, Daniella Landau, Esther Manor, et al.
Investigative Ophthalmology & Visual Science|April 27, 2007
Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataractDavid Cohen, Udy Bar-Yosef, Jaime Levy, et al.
American Journal of Human Genetics|July 20, 2004
Comparative genomic analysis identifies an ADP-ribosylation factor-like gene as the cause of Bardet-Biedl syndrome (BBS3)Annie P Chiang, Darryl Nishimura, Charles Searby, et al.
Nature Genetics|May 29, 2002
Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemiaRoxanne Y Walder, Daniel Landau, Peter Meyer, et al.
European Journal of Human Genetics : EJHG|August 9, 2007
Population history and infrequent mutations: how old is a rare mutation? GUCY2D as a worked exampleSylvain Hanein, Isabelle Perrault, Sylvie Gerber, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 13, 2004
Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsinDarryl Y Nishimura, Melissa Fath, Robert F Mullins, et al.
Lancet (London, England)|April 7, 2005
Promoting Arab and Israeli cooperation: peacebuilding through health initiativesHarvey Skinner, Ziad Abdeen, Hani Abdeen, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 12, 2006
Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)Annie P Chiang, John S Beck, Hsan-Jan Yen, et al.
Nature Genetics|July 16, 2002
Identification of the gene (BBS1) most commonly involved in Bardet-Biedl syndrome, a complex human obesity syndromeKirk Mykytyn, Darryl Y Nishimura, Charles C Searby, et al.
Pageof 3