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N C Nevin

Showing results (151-160 of 223) with videos related to

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British Medical Journal|October 9, 1971
Chromosome analysis before birth and its value in genetic counsellingM E Ferguson-Smith, M A Ferguson-Smith, N C Nevin, et al.
Biology and Society : the Journal of the Eugenics Society|June 1, 1987
Report of the delegation of clinical geneticists to China, Spring 1986M Laurence, P S Harper, R Harris, et al.
The Journal of Investigative Dermatology|December 24, 1997
A novel mutation in the helix termination peptide of keratin 5 causing epidermolysis bullosa simplex Dowling-MearaA D Irvine, K E McKenna, A Bingham, et al.
The British Journal of Dermatology|October 1, 1972
Atypical erythrokeratoderma with deafness, physical retardation and peripheral neuropathyJ M Beare, N C Nevin, P Froggatt, et al.
Lancet (London, England)|May 12, 1990
Prenatal diagnosis of mucolipidosis II by early amniocentesisG T Besley, D M Broadhead, N C Nevin, et al.
The British Journal of Ophthalmology|August 1, 1992
Prenatal exclusion of Norrie's diseaseR M Redmond, C A Graham, E D Kelly, et al.
American Journal of Medical Genetics|April 11, 2000
First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISHM Bhat, P J Morrison, A Getty, et al.
Human Mutation|January 1, 1994
Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosisJ Zschocke, C A Graham, F J Stewart, et al.
Biochemical Society Transactions|April 1, 1990
Localization of a human fibroblast extracellular protein in cells and tissues by monoclonal antibodyW H McLean, J C Orchin, H Foster, et al.
The British Journal of Dermatology|February 1, 1982
Letterer-Siwe disease: a study of thirteen cases over a 21 - year periodE A Bingham, J M Bridges, A M Kelly, et al.
Pageof 23

Showing results (151-160 of 223) with videos related to

Sort By:
Pageof 23
British Medical Journal|October 9, 1971
Chromosome analysis before birth and its value in genetic counsellingM E Ferguson-Smith, M A Ferguson-Smith, N C Nevin, et al.
Biology and Society : the Journal of the Eugenics Society|June 1, 1987
Report of the delegation of clinical geneticists to China, Spring 1986M Laurence, P S Harper, R Harris, et al.
The Journal of Investigative Dermatology|December 24, 1997
A novel mutation in the helix termination peptide of keratin 5 causing epidermolysis bullosa simplex Dowling-MearaA D Irvine, K E McKenna, A Bingham, et al.
The British Journal of Dermatology|October 1, 1972
Atypical erythrokeratoderma with deafness, physical retardation and peripheral neuropathyJ M Beare, N C Nevin, P Froggatt, et al.
Lancet (London, England)|May 12, 1990
Prenatal diagnosis of mucolipidosis II by early amniocentesisG T Besley, D M Broadhead, N C Nevin, et al.
The British Journal of Ophthalmology|August 1, 1992
Prenatal exclusion of Norrie's diseaseR M Redmond, C A Graham, E D Kelly, et al.
American Journal of Medical Genetics|April 11, 2000
First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISHM Bhat, P J Morrison, A Getty, et al.
Human Mutation|January 1, 1994
Non-phenylketonuria hyperphenylalaninaemia in Northern Ireland: frequent mutation allows screening and early diagnosisJ Zschocke, C A Graham, F J Stewart, et al.
Biochemical Society Transactions|April 1, 1990
Localization of a human fibroblast extracellular protein in cells and tissues by monoclonal antibodyW H McLean, J C Orchin, H Foster, et al.
The British Journal of Dermatology|February 1, 1982
Letterer-Siwe disease: a study of thirteen cases over a 21 - year periodE A Bingham, J M Bridges, A M Kelly, et al.
Pageof 23