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Human Mutation
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August 26, 2003
PTEN: one gene, many syndromes
Charis Eng
Human Mutation
|
August 26, 2003
Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs
Shaun S Abeysinghe, Nadia Chuzhanova, Michael Krawczak, et al.
Human Mutation
|
August 26, 2003
CFTR mutations in patients from Colombia: implications for local and regional molecular diagnosis programs
Genoveva Keyeux, Clemencia Rodas, Thierry Bienvenu, et al.
Human Mutation
|
January 1, 1992
Analysis of exon 7 of the human phenylalanine hydroxylase gene: a mutation hot spot?
B Dworniczak, L Kalaydjieva, S Pankoke, et al.
Human Mutation
|
November 25, 2003
Mutational spectrum of the succinate semialdehyde dehydrogenase (ALDH5A1) gene and functional analysis of 27 novel disease-causing mutations in patients with SSADH deficiency
Shinjiro Akaboshi, Boris M Hogema, Andrea Novelletto, et al.
Human Mutation
|
November 25, 2003
Novel cytochrome P450 1B1 (CYP1B1) mutations in patients with primary congenital glaucoma in France
Evelyne Colomb, Josseline Kaplan, Henri-Jean Garchon
Human Mutation
|
November 25, 2003
A pathogenic glutamate-to-aspartate substitution (D296E) in the pyruvate dehydrogenase E1 subunit gene PDHA1
R M Brown, R A Head, I I Boubriak, et al.
Human Mutation
|
October 27, 2007
Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs)
M Upadhyaya, Lan Kluwe, G Spurlock, et al.
Human Mutation
|
October 17, 2007
AVPR1A and OXTR polymorphisms are associated with sexual and reproductive behavioral phenotypes in humans. Mutation in brief no. 981. Online
Zoë M Prichard, Andrew J Mackinnon, Anthony F Jorm, et al.
Human Mutation
|
April 27, 2007
Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency
Sacha Ferdinandusse, Simone Denis, Eveline M Hogenhout, et al.
Page
of 655
Search research articles
Search
Showing results (771-780 of 6,545) with videos related to
Sort By:
Page
of 655
Human Mutation
|
August 26, 2003
PTEN: one gene, many syndromes
Charis Eng
Human Mutation
|
August 26, 2003
Translocation and gross deletion breakpoints in human inherited disease and cancer I: Nucleotide composition and recombination-associated motifs
Shaun S Abeysinghe, Nadia Chuzhanova, Michael Krawczak, et al.
Human Mutation
|
August 26, 2003
CFTR mutations in patients from Colombia: implications for local and regional molecular diagnosis programs
Genoveva Keyeux, Clemencia Rodas, Thierry Bienvenu, et al.
Human Mutation
|
January 1, 1992
Analysis of exon 7 of the human phenylalanine hydroxylase gene: a mutation hot spot?
B Dworniczak, L Kalaydjieva, S Pankoke, et al.
Human Mutation
|
November 25, 2003
Mutational spectrum of the succinate semialdehyde dehydrogenase (ALDH5A1) gene and functional analysis of 27 novel disease-causing mutations in patients with SSADH deficiency
Shinjiro Akaboshi, Boris M Hogema, Andrea Novelletto, et al.
Human Mutation
|
November 25, 2003
Novel cytochrome P450 1B1 (CYP1B1) mutations in patients with primary congenital glaucoma in France
Evelyne Colomb, Josseline Kaplan, Henri-Jean Garchon
Human Mutation
|
November 25, 2003
A pathogenic glutamate-to-aspartate substitution (D296E) in the pyruvate dehydrogenase E1 subunit gene PDHA1
R M Brown, R A Head, I I Boubriak, et al.
Human Mutation
|
October 27, 2007
Germline and somatic NF1 gene mutation spectrum in NF1-associated malignant peripheral nerve sheath tumors (MPNSTs)
M Upadhyaya, Lan Kluwe, G Spurlock, et al.
Human Mutation
|
October 17, 2007
AVPR1A and OXTR polymorphisms are associated with sexual and reproductive behavioral phenotypes in humans. Mutation in brief no. 981. Online
Zoë M Prichard, Andrew J Mackinnon, Anthony F Jorm, et al.
Human Mutation
|
April 27, 2007
Clinical, biochemical, and mutational spectrum of peroxisomal acyl-coenzyme A oxidase deficiency
Sacha Ferdinandusse, Simone Denis, Eveline M Hogenhout, et al.
Page
of 655