Search research articles
Contact Us
Filters
Showing results (161-170 of 11,257) with videos related to
Page
of 1,126
Sort By:
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 2011
Joyce C Harper, Sioban B Sengupta
Human Genetics
|
June 1, 1990
The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions
D N Cooper, M Krawczak
Human Genetics
|
September 17, 2011
The genetics of kidney transplantation
Nicolas 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 children
Collins 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 17
S 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 GPATCH8
Hiroshi 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 carcinoma
Dipanjana Mazumder Indra, Sraboni Mitra, Anup Roy, et al.
Human Genetics
|
June 11, 2011
A scaffold for X chromosome inactivation
Anna 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 risk
Chang Sun, Dezheng Huo, Catherine Southard, et al.
Page
of 1,126
Search research articles
Search
Showing results (161-170 of 11,257) with videos related to
Sort By:
Page
of 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 2011
Joyce C Harper, Sioban B Sengupta
Human Genetics
|
June 1, 1990
The mutational spectrum of single base-pair substitutions causing human genetic disease: patterns and predictions
D N Cooper, M Krawczak
Human Genetics
|
September 17, 2011
The genetics of kidney transplantation
Nicolas 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 children
Collins 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 17
S 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 GPATCH8
Hiroshi 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 carcinoma
Dipanjana Mazumder Indra, Sraboni Mitra, Anup Roy, et al.
Human Genetics
|
June 11, 2011
A scaffold for X chromosome inactivation
Anna 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 risk
Chang Sun, Dezheng Huo, Catherine Southard, et al.
Page
of 1,126