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Genomics
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January 1, 1990
The human metallothionein gene cluster is not disrupted in myelomonocytic leukemia
G R Sutherland, E Baker, D F Callen, et al.
Mutation Research
|
January 1, 1977
Mutation induction by the antischistosomal drug F30066 in various test systems
T M Ong, D F Callen, S L Huang, et al.
Human Molecular Genetics
|
September 1, 1994
Microsatellite repeat polymorphism at the D16S366 locus
E A Schultz, D F Callen, N A Doggett, et al.
Journal of Medical Genetics
|
March 1, 1990
Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16
D F Callen, M L Ringenbergs, J C Fowler, et al.
American Journal of Medical Genetics
|
April 1, 1989
Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q
E A Haan, Y J Hull, S White, et al.
Genomics
|
September 11, 2001
Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein
G Kremmidiotis, A E Gardner, C Settasatian, et al.
Human Genetics
|
June 1, 1988
Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14
D A Robertson, D F Callen, E G Baker, et al.
Chromosoma
|
October 1, 1989
Human satellite III DNA: genomic location and sequence homogeneity of the TaqI-deficient polymorphic sequences
J C Fowler, L A Burgoyne, E G Baker, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Integration of the cytogenetic and genetic linkage maps of human chromosome 16 using 50 physical intervals and 50 polymorphic loci
H M Kozman, H A Phillips, D F Callen, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11
C Jeanpierre, S A Whitmore, E Austruy, et al.
Page
of 20
Search research articles
Search
Showing results (61-70 of 195) with videos related to
Sort By:
Page
of 20
Genomics
|
January 1, 1990
The human metallothionein gene cluster is not disrupted in myelomonocytic leukemia
G R Sutherland, E Baker, D F Callen, et al.
Mutation Research
|
January 1, 1977
Mutation induction by the antischistosomal drug F30066 in various test systems
T M Ong, D F Callen, S L Huang, et al.
Human Molecular Genetics
|
September 1, 1994
Microsatellite repeat polymorphism at the D16S366 locus
E A Schultz, D F Callen, N A Doggett, et al.
Journal of Medical Genetics
|
March 1, 1990
Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16
D F Callen, M L Ringenbergs, J C Fowler, et al.
American Journal of Medical Genetics
|
April 1, 1989
Tricho-rhino-phalangeal and branchio-oto syndromes in a family with an inherited rearrangement of chromosome 8q
E A Haan, Y J Hull, S White, et al.
Genomics
|
September 11, 2001
Molecular and functional analyses of the human and mouse genes encoding AFG3L1, a mitochondrial metalloprotease homologous to the human spastic paraplegia protein
G Kremmidiotis, A E Gardner, C Settasatian, et al.
Human Genetics
|
June 1, 1988
Chromosomal localization of the gene for human glucosamine-6-sulphatase to 12q14
D A Robertson, D F Callen, E G Baker, et al.
Chromosoma
|
October 1, 1989
Human satellite III DNA: genomic location and sequence homogeneity of the TaqI-deficient polymorphic sequences
J C Fowler, L A Burgoyne, E G Baker, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Integration of the cytogenetic and genetic linkage maps of human chromosome 16 using 50 physical intervals and 50 polymorphic loci
H M Kozman, H A Phillips, D F Callen, et al.
Cytogenetics and Cell Genetics
|
January 1, 1993
Chromosomal assignment of the uromodulin gene (UMOD) to 16p13.11
C Jeanpierre, S A Whitmore, E Austruy, et al.
Page
of 20