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C G Mathew

Showing results (41-50 of 129) with videos related to

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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2000
Prenatal onset spinal muscular atrophyM J MacLeod, J E Taylor, P W Lunt, et al.
British Journal of Haematology|July 1, 1996
Fanconi's anaemia presenting as acute myeloid leukaemia in adulthoodJ D Cavenagh, D S Richardson, R A Gibson, et al.
Nucleic Acids Research|December 11, 1979
Analysis of the high mobility group proteins associated with salt-soluble nucleosomesG H Goodwin, C G Mathew, C A Wright, et al.
British Journal of Cancer|March 1, 1995
Loss of heterozygosity of the oestrogen receptor gene in breast cancerH Iwase, J M Greenman, D M Barnes, et al.
Human Molecular Genetics|February 7, 2001
Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathwayA L Medhurst, P A Huber, Q Waisfisz, et al.
Lancet (London, England)|May 14, 1994
Rapid molecular method for prenatal detection of Down's syndromeB Pertl, S C Yau, J Sherlock, et al.
Lancet (London, England)|October 23, 1993
Cytogenetic versus DNA diagnosis in routine referrals for fragile X syndromeQ Wang, E Green, A Barnicoat, et al.
Cancer Letters|November 29, 1996
Sequence variants of the estrogen receptor (ER) gene found in breast cancer patients with ER negative and progesterone receptor positive tumorsH Iwase, J M Greenman, D M Barnes, et al.
Annals of Human Genetics|December 4, 2003
SNP subset selection for genetic association studiesM C Byng, J C Whittaker, A P Cuthbert, et al.
Journal of Medical Genetics|June 1, 1993
Osteogenesis imperfecta type III: mutations in the type I collagen structural genes, COL1A1 and COL1A2, are not necessarily responsibleG A Wallis, B Sykes, P H Byers, et al.
Pageof 13

Showing results (41-50 of 129) with videos related to

Sort By:
Pageof 13
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 4, 2000
Prenatal onset spinal muscular atrophyM J MacLeod, J E Taylor, P W Lunt, et al.
British Journal of Haematology|July 1, 1996
Fanconi's anaemia presenting as acute myeloid leukaemia in adulthoodJ D Cavenagh, D S Richardson, R A Gibson, et al.
Nucleic Acids Research|December 11, 1979
Analysis of the high mobility group proteins associated with salt-soluble nucleosomesG H Goodwin, C G Mathew, C A Wright, et al.
British Journal of Cancer|March 1, 1995
Loss of heterozygosity of the oestrogen receptor gene in breast cancerH Iwase, J M Greenman, D M Barnes, et al.
Human Molecular Genetics|February 7, 2001
Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathwayA L Medhurst, P A Huber, Q Waisfisz, et al.
Lancet (London, England)|May 14, 1994
Rapid molecular method for prenatal detection of Down's syndromeB Pertl, S C Yau, J Sherlock, et al.
Lancet (London, England)|October 23, 1993
Cytogenetic versus DNA diagnosis in routine referrals for fragile X syndromeQ Wang, E Green, A Barnicoat, et al.
Cancer Letters|November 29, 1996
Sequence variants of the estrogen receptor (ER) gene found in breast cancer patients with ER negative and progesterone receptor positive tumorsH Iwase, J M Greenman, D M Barnes, et al.
Annals of Human Genetics|December 4, 2003
SNP subset selection for genetic association studiesM C Byng, J C Whittaker, A P Cuthbert, et al.
Journal of Medical Genetics|June 1, 1993
Osteogenesis imperfecta type III: mutations in the type I collagen structural genes, COL1A1 and COL1A2, are not necessarily responsibleG A Wallis, B Sykes, P H Byers, et al.
Pageof 13