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Human genetics

Showing results (561-570 of 11,264) with videos related to

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Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ABCA4. Disease: Stargardt diseaseJana Aguirre-Lamban, R Riveiro-Alvarez, M Garcia-Hoyos, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: CitrullinaemiaDavid Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: CPOX. Disease: CoproporphyriaSabrina Ausenda, E Di Pierro, V Brancaleoni, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: HBB. Disease: haemoglobin variantChiara Refaldi, Claudia Cesaretti, Maria Rosaria Fasulo, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndromeDaniela Marchetti, M R Iascone, L Pezzoli
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: LDLR. Disease: hypercholesterolemiaM S Katrina Kotzer, Linnea Baudhuin
Human Genetics|April 6, 2010
A single nucleotide polymorphism in the FADS1/FADS2 gene is associated with plasma lipid profiles in two genetically similar Asian ethnic groups with distinctive differences in lifestyleKazuhiro Nakayama, Tumenbayer Bayasgalan, Fumiko Tazoe, et al.
Human Genetics|April 13, 2010
Replication and extension of association of choline acetyltransferase with nicotine dependence in European and African American smokersJinxue Wei, Jennie Z Ma, Thomas J Payne, et al.
Human Genetics|June 1, 1991
Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniquesW Van Hul, H Backhovens, G Van Camp, et al.
Human Genetics|June 1, 1991
Cysteine in the triple helical domain of the pro alpha 2(I) chain of type-I collagen in nonlethal forms of osteogenesis imperfectaD H Cohn, P H Byers
Pageof 1,127

Showing results (561-570 of 11,264) with videos related to

Sort By:
Pageof 1,127
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ABCA4. Disease: Stargardt diseaseJana Aguirre-Lamban, R Riveiro-Alvarez, M Garcia-Hoyos, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: ASS1. Disease: CitrullinaemiaDavid Dimmock, Pamela Trapane, Annette Feigenbaum, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: CPOX. Disease: CoproporphyriaSabrina Ausenda, E Di Pierro, V Brancaleoni, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: HBB. Disease: haemoglobin variantChiara Refaldi, Claudia Cesaretti, Maria Rosaria Fasulo, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: JAG1. Disease: Alagille syndromeDaniela Marchetti, M R Iascone, L Pezzoli
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: LDLR. Disease: hypercholesterolemiaM S Katrina Kotzer, Linnea Baudhuin
Human Genetics|April 6, 2010
A single nucleotide polymorphism in the FADS1/FADS2 gene is associated with plasma lipid profiles in two genetically similar Asian ethnic groups with distinctive differences in lifestyleKazuhiro Nakayama, Tumenbayer Bayasgalan, Fumiko Tazoe, et al.
Human Genetics|April 13, 2010
Replication and extension of association of choline acetyltransferase with nicotine dependence in European and African American smokersJinxue Wei, Jennie Z Ma, Thomas J Payne, et al.
Human Genetics|June 1, 1991
Subregional localization of the chromosome 21 loci D21S24 and D21S26 using physical mapping techniquesW Van Hul, H Backhovens, G Van Camp, et al.
Human Genetics|June 1, 1991
Cysteine in the triple helical domain of the pro alpha 2(I) chain of type-I collagen in nonlethal forms of osteogenesis imperfectaD H Cohn, P H Byers
Pageof 1,127