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Human Genetics
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June 1, 1991
The importance of further cytogenetic and molecular investigation of acrocentric variants: justification by presentation of a case [t(8;14)(q24;p11)]
L Hills, E Earle, M Wilson, et al.
Human Genetics
|
June 1, 1991
The human kininogen gene (KNG) mapped to chromosome 3q26-qter by analysis of somatic cell hybrids using the polymerase chain reaction
D Fong, D I Smith, W T Hsieh
Human Genetics
|
August 11, 2010
Age at onset in Huntington's disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7
Silke Metzger, Meiju Saukko, Hong Van Che, et al.
Human Genetics
|
August 12, 2010
Achalasia: will genetic studies provide insights?
Henning R Gockel, Johannes Schumacher, Ines Gockel, et al.
Human Genetics
|
May 16, 1978
Hereditary sensory neuropathy, a new type
A Staal, K Mechelse
Human Genetics
|
June 1, 1991
Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus
G M Glenn, L N Daniel, P Choyke, et al.
Human Genetics
|
June 1, 1991
DNA diagnosis of hydatidiform mole using the polymerase chain reaction
R Fukuyama, M Takata, J Kudoh, et al.
Human Genetics
|
June 1, 1991
Regional chromosomal assignment of human 3-beta-hydroxy-5-ene steroid dehydrogenase to 1p13.1 by non-isotopic in situ hybridisation
N Morrison, D A Nickson, M W McBride, et al.
Human Genetics
|
June 1, 1991
Chromosomal assignment of a large tRNA gene cluster (tRNA(Leu), tRNA(Gln), tRNA(Lys), tRNA(Arg), tRNA(Gly)) to 17p13.1
N Morrison, J P Goddard, D H Ledbetter, et al.
Human Genetics
|
July 7, 2010
Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test
María M Abad-Grau, Nuria Medina-Medina, Rosana Montes-Soldado, et al.
Page
of 1,127
Search research articles
Search
Showing results (571-580 of 11,264) with videos related to
Sort By:
Page
of 1,127
Human Genetics
|
June 1, 1991
The importance of further cytogenetic and molecular investigation of acrocentric variants: justification by presentation of a case [t(8;14)(q24;p11)]
L Hills, E Earle, M Wilson, et al.
Human Genetics
|
June 1, 1991
The human kininogen gene (KNG) mapped to chromosome 3q26-qter by analysis of somatic cell hybrids using the polymerase chain reaction
D Fong, D I Smith, W T Hsieh
Human Genetics
|
August 11, 2010
Age at onset in Huntington's disease is modified by the autophagy pathway: implication of the V471A polymorphism in Atg7
Silke Metzger, Meiju Saukko, Hong Van Che, et al.
Human Genetics
|
August 12, 2010
Achalasia: will genetic studies provide insights?
Henning R Gockel, Johannes Schumacher, Ines Gockel, et al.
Human Genetics
|
May 16, 1978
Hereditary sensory neuropathy, a new type
A Staal, K Mechelse
Human Genetics
|
June 1, 1991
Von Hippel-Lindau (VHL) disease: distinct phenotypes suggest more than one mutant allele at the VHL locus
G M Glenn, L N Daniel, P Choyke, et al.
Human Genetics
|
June 1, 1991
DNA diagnosis of hydatidiform mole using the polymerase chain reaction
R Fukuyama, M Takata, J Kudoh, et al.
Human Genetics
|
June 1, 1991
Regional chromosomal assignment of human 3-beta-hydroxy-5-ene steroid dehydrogenase to 1p13.1 by non-isotopic in situ hybridisation
N Morrison, D A Nickson, M W McBride, et al.
Human Genetics
|
June 1, 1991
Chromosomal assignment of a large tRNA gene cluster (tRNA(Leu), tRNA(Gln), tRNA(Lys), tRNA(Arg), tRNA(Gly)) to 17p13.1
N Morrison, J P Goddard, D H Ledbetter, et al.
Human Genetics
|
July 7, 2010
Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test
María M Abad-Grau, Nuria Medina-Medina, Rosana Montes-Soldado, et al.
Page
of 1,127