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Human Genetics
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June 1, 1995
Highly polymorphic dinucleotide repeat at the NF2 gene
D Bourn, T Strachan
Human Genetics
|
May 1, 1995
Eleven novel mutations in the NF2 tumour suppressor gene
D Bourn, G Evans, S Mason, 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 1, 1991
Extended MHC haplotypes and CYP21/C4 gene organisation in Irish 21-hydroxylase deficiency families
P J Sinnott, C Costigan, P A Dyer, et al.
Human Genetics
|
October 1, 1990
Molecular analysis of the human MHC class I region in hereditary haemochromatosis. A study by pulsed-field gel electrophoresis
D K Lord, I Dunham, R D Campbell, et al.
Human Genetics
|
March 1, 1992
CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency families
P J Sinnott, C Livieri, M Sampietro, et al.
Human Genetics
|
September 10, 1999
Genomic organisation of the human chordin gene and mutation screening of candidate Cornelia de Lange syndrome genes
M Smith, S Herrell, M Lusher, et al.
Human Genetics
|
May 26, 1998
Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly
F R Vargas, E Roessler, K Gaudenz, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Human Genetics
|
June 1, 1995
Highly polymorphic dinucleotide repeat at the NF2 gene
D Bourn, T Strachan
Human Genetics
|
May 1, 1995
Eleven novel mutations in the NF2 tumour suppressor gene
D Bourn, G Evans, S Mason, 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 1, 1991
Extended MHC haplotypes and CYP21/C4 gene organisation in Irish 21-hydroxylase deficiency families
P J Sinnott, C Costigan, P A Dyer, et al.
Human Genetics
|
October 1, 1990
Molecular analysis of the human MHC class I region in hereditary haemochromatosis. A study by pulsed-field gel electrophoresis
D K Lord, I Dunham, R D Campbell, et al.
Human Genetics
|
March 1, 1992
CYP21/C4 gene organisation in Italian 21-hydroxylase deficiency families
P J Sinnott, C Livieri, M Sampietro, et al.
Human Genetics
|
September 10, 1999
Genomic organisation of the human chordin gene and mutation screening of candidate Cornelia de Lange syndrome genes
M Smith, S Herrell, M Lusher, et al.
Human Genetics
|
May 26, 1998
Analysis of the human Sonic Hedgehog coding and promoter regions in sacral agenesis, triphalangeal thumb, and mirror polydactyly
F R Vargas, E Roessler, K Gaudenz, et al.
Page
of 1