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The American Journal of Surgical Pathology
|
July 1, 1984
Infantile myofibromatosis. Evidence for an autosomal-dominant disorder
T A Jennings, P H Duray, F S Collins, et al.
Human Molecular Genetics
|
July 1, 1993
Dinucleotide repeat polymorphisms at the D4S126 and D4S114 loci
D A Tagle, K L Blanchard-McQuate, J Valdes, et al.
Human Molecular Genetics
|
July 1, 1993
A compound nucleotide repeat in the neurofibromatosis (NF1) gene
L B Andersen, S A Tarlé, D A Marchuk, et al.
Human Molecular Genetics
|
May 1, 1994
Ten base pair duplication in exon 38 of the NF1 gene
E Legius, B K Hall, M R Wallace, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1984
G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene
F S Collins, C J Stoeckert, G R Serjeant, et al.
Somatic Cell and Molecular Genetics
|
September 1, 1996
Chromosomal localization of 15 ion channel genes
M W Russell, S du Manoir, D J Munroe, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Nuclear proteins which bind the human gamma-globin gene
D L Gumucio, T A Gray, K L Rood, et al.
Nucleic Acids Research
|
August 25, 1987
SacI RFLP in the human von Willebrand factor gene
B A Konkle, S Kim, M C Iannuzzi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1993
Functional roles of the nucleotide-binding folds in the activation of the cystic fibrosis transmembrane conductance regulator
L S Smit, D J Wilkinson, M K Mansoura, et al.
Journal of Neuroscience Research
|
October 1, 1993
Modulation of the neurofibromatosis type 1 gene product, neurofibromin, during Schwann cell differentiation
D H Gutmann, G I Tennekoon, J L Cole, et al.
Page
of 30
Search research articles
Search
Showing results (111-120 of 297) with videos related to
Sort By:
Page
of 30
The American Journal of Surgical Pathology
|
July 1, 1984
Infantile myofibromatosis. Evidence for an autosomal-dominant disorder
T A Jennings, P H Duray, F S Collins, et al.
Human Molecular Genetics
|
July 1, 1993
Dinucleotide repeat polymorphisms at the D4S126 and D4S114 loci
D A Tagle, K L Blanchard-McQuate, J Valdes, et al.
Human Molecular Genetics
|
July 1, 1993
A compound nucleotide repeat in the neurofibromatosis (NF1) gene
L B Andersen, S A Tarlé, D A Marchuk, et al.
Human Molecular Genetics
|
May 1, 1994
Ten base pair duplication in exon 38 of the NF1 gene
E Legius, B K Hall, M R Wallace, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
August 1, 1984
G gamma beta+ hereditary persistence of fetal hemoglobin: cosmid cloning and identification of a specific mutation 5' to the G gamma gene
F S Collins, C J Stoeckert, G R Serjeant, et al.
Somatic Cell and Molecular Genetics
|
September 1, 1996
Chromosomal localization of 15 ion channel genes
M W Russell, S du Manoir, D J Munroe, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Nuclear proteins which bind the human gamma-globin gene
D L Gumucio, T A Gray, K L Rood, et al.
Nucleic Acids Research
|
August 25, 1987
SacI RFLP in the human von Willebrand factor gene
B A Konkle, S Kim, M C Iannuzzi, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
November 1, 1993
Functional roles of the nucleotide-binding folds in the activation of the cystic fibrosis transmembrane conductance regulator
L S Smit, D J Wilkinson, M K Mansoura, et al.
Journal of Neuroscience Research
|
October 1, 1993
Modulation of the neurofibromatosis type 1 gene product, neurofibromin, during Schwann cell differentiation
D H Gutmann, G I Tennekoon, J L Cole, et al.
Page
of 30