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Human genetics

Showing results (161-170 of 11,257) with videos related to

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Human Genetics|July 8, 2011
Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH)Shin Hayashi, Nobuhiko Okamoto, Yasutsugu Chinen, et al.
Human Genetics|July 13, 2011
Preimplantation genetic diagnosis: state of the art 2011Joyce C Harper, Sioban B Sengupta
Human Genetics|June 1, 1990
The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictionsD N Cooper, M Krawczak
Human Genetics|September 17, 2011
The genetics of kidney transplantationNicolas Pallet, Eric Thervet
Human Genetics|August 6, 2011
Functional haplotypes of Fc gamma (Fcγ) receptor (FcγRIIA and FcγRIIIB) predict risk to repeated episodes of severe malarial anemia and mortality in Kenyan childrenCollins Ouma, Gregory C Davenport, Steven Garcia, et al.
Human Genetics|June 1, 1990
The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17S M Pulst, J M Graham, P Fain, et al.
Human Genetics|May 20, 2011
Hyperuricemia cosegregating with osteogenesis imperfecta is associated with a mutation in GPATCH8Hiroshi Kaneko, Hiroshi Kitoh, Tohru Matsuura, et al.
Human Genetics|June 7, 2011
Alterations of ATM and CADM1 in chromosomal 11q22.3-23.2 region are associated with the development of invasive cervical carcinomaDipanjana Mazumder Indra, Sraboni Mitra, Anup Roy, et al.
Human Genetics|June 11, 2011
A scaffold for X chromosome inactivationAnna Tattermusch, Neil Brockdorff
Human Genetics|June 11, 2011
A signature of balancing selection in the region upstream to the human UGT2B4 gene and implications for breast cancer riskChang Sun, Dezheng Huo, Catherine Southard, et al.
Pageof 1,126

Showing results (161-170 of 11,257) with videos related to

Sort By:
Pageof 1,126
Human Genetics|July 8, 2011
Novel intragenic duplications and mutations of CASK in patients with mental retardation and microcephaly with pontine and cerebellar hypoplasia (MICPCH)Shin Hayashi, Nobuhiko Okamoto, Yasutsugu Chinen, et al.
Human Genetics|July 13, 2011
Preimplantation genetic diagnosis: state of the art 2011Joyce C Harper, Sioban B Sengupta
Human Genetics|June 1, 1990
The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictionsD N Cooper, M Krawczak
Human Genetics|September 17, 2011
The genetics of kidney transplantationNicolas Pallet, Eric Thervet
Human Genetics|August 6, 2011
Functional haplotypes of Fc gamma (Fcγ) receptor (FcγRIIA and FcγRIIIB) predict risk to repeated episodes of severe malarial anemia and mortality in Kenyan childrenCollins Ouma, Gregory C Davenport, Steven Garcia, et al.
Human Genetics|June 1, 1990
The achondroplasia gene is not linked to the locus for neurofibromatosis 1 on chromosome 17S M Pulst, J M Graham, P Fain, et al.
Human Genetics|May 20, 2011
Hyperuricemia cosegregating with osteogenesis imperfecta is associated with a mutation in GPATCH8Hiroshi Kaneko, Hiroshi Kitoh, Tohru Matsuura, et al.
Human Genetics|June 7, 2011
Alterations of ATM and CADM1 in chromosomal 11q22.3-23.2 region are associated with the development of invasive cervical carcinomaDipanjana Mazumder Indra, Sraboni Mitra, Anup Roy, et al.
Human Genetics|June 11, 2011
A scaffold for X chromosome inactivationAnna Tattermusch, Neil Brockdorff
Human Genetics|June 11, 2011
A signature of balancing selection in the region upstream to the human UGT2B4 gene and implications for breast cancer riskChang Sun, Dezheng Huo, Catherine Southard, et al.
Pageof 1,126