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D T Bonthron

Showing results (11-20 of 56) with videos related to

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Human Genetics|December 22, 1999
Complex patterns of intragenic polymorphism at the PDGFA locusD T Bonthron, S J Smith, R Campbell
Nucleic Acids Research|July 25, 1991
SmaI and HhaI polymorphisms in the 5' region of the human von Willebrand factor gene (F8VWF)L Strain, D T Bonthron, D J Brock
Clinical Genetics|March 1, 1993
Nager acrofacial dysostosis: minor familial manifestations supporting dominant inheritanceD T Bonthron, D F Macgregor, D G Barr
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1997
The genes encoding glucokinase regulatory protein and ketohexokinase co-localize to mouse chromosome 5P J Wightman, B E Hayward, D T Bonthron
Human Genetics|October 13, 2000
Characterization of TH1 and CTSZ, two non-imprinted genes downstream of GNAS1 in chromosome 20q13D T Bonthron, B E Hayward, V Moran, et al.
Nature Genetics|October 1, 1995
A human parthenogenetic chimaeraL Strain, J P Warner, T Johnston, et al.
American Journal of Human Genetics|February 1, 1994
Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3L Strain, C M Gosden, D J Brock, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 23, 1998
Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteinsB E Hayward, V Moran, L Strain, et al.
Human Molecular Genetics|September 1, 1994
Molecular basis of essential fructosuria: molecular cloning and mutational analysis of human ketohexokinase (fructokinase)D T Bonthron, N Brady, I A Donaldson, et al.
Biochemical Society Transactions|July 27, 2005
Phenotype associated with recessively inherited mutations in DNA mismatch repair (MMR) genesM de Vos, B Hayward, D T Bonthron, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
Human Genetics|December 22, 1999
Complex patterns of intragenic polymorphism at the PDGFA locusD T Bonthron, S J Smith, R Campbell
Nucleic Acids Research|July 25, 1991
SmaI and HhaI polymorphisms in the 5' region of the human von Willebrand factor gene (F8VWF)L Strain, D T Bonthron, D J Brock
Clinical Genetics|March 1, 1993
Nager acrofacial dysostosis: minor familial manifestations supporting dominant inheritanceD T Bonthron, D F Macgregor, D G Barr
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 1, 1997
The genes encoding glucokinase regulatory protein and ketohexokinase co-localize to mouse chromosome 5P J Wightman, B E Hayward, D T Bonthron
Human Genetics|October 13, 2000
Characterization of TH1 and CTSZ, two non-imprinted genes downstream of GNAS1 in chromosome 20q13D T Bonthron, B E Hayward, V Moran, et al.
Nature Genetics|October 1, 1995
A human parthenogenetic chimaeraL Strain, J P Warner, T Johnston, et al.
American Journal of Human Genetics|February 1, 1994
Genetic heterogeneity in X-linked hydrocephalus: linkage to markers within Xq27.3L Strain, C M Gosden, D J Brock, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 23, 1998
Bidirectional imprinting of a single gene: GNAS1 encodes maternally, paternally, and biallelically derived proteinsB E Hayward, V Moran, L Strain, et al.
Human Molecular Genetics|September 1, 1994
Molecular basis of essential fructosuria: molecular cloning and mutational analysis of human ketohexokinase (fructokinase)D T Bonthron, N Brady, I A Donaldson, et al.
Biochemical Society Transactions|July 27, 2005
Phenotype associated with recessively inherited mutations in DNA mismatch repair (MMR) genesM de Vos, B Hayward, D T Bonthron, et al.
Pageof 6