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N J Lench

Showing results (1-10 of 39) with videos related to

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Human Mutation|January 1, 1995
Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1)N J Lench, G B Winter
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|March 1, 1997
DNA diagnosis of X-linked amelogenesis imperfecta (AIH1)N J Lench, A H Brook
Human Genetics|April 1, 1997
The human gene encoding FKBP-rapamycin associated protein (FRAP) maps to chromosomal band 1p36.2N J Lench, R Macadam, A F Markham
Molecular Pathology : MP|August 26, 1998
Evidence for a common mutation in hereditary pancreatitisS M Bell, C Bennett, A F Markham, et al.
Biochimica Et Biophysica Acta|October 19, 1999
Isolation and characterisation of a cDNA encoding the precursor for a novel member of the acyl-CoA dehydrogenase gene familyE A Telford, L M Moynihan, A F Markham, et al.
Current Opinion in Biotechnology|December 1, 1994
Comparative genetic mapping for the identification of novel diagnostic and therapeutic targetsP L Coletta, N J Lench, K A Brown, et al.
Nucleic Acids Research|June 1, 1996
Vectorette PCR isolation of microsatellite repeat sequences using anchored dinucleotide repeat primersN J Lench, A Norris, A Bailey, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|June 1, 1995
Immunoglobulin gene rearrangements in lymphoplasmacytic infiltrates of labial salivary glands in Sjögren's syndrome. A possible predictor of lymphoma developmentR Jordan, T C Diss, N J Lench, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutationT P Hutchin, N J Lench, S Arbuzova, et al.
International Journal of Radiation Biology|December 1, 1994
DNA marker D11S384 shows zero recombination with the ataxia-telangiectasia locus in North American familiesN J Lench, P Athma, A Ottaiano, et al.
Pageof 4

Showing results (1-10 of 39) with videos related to

Sort By:
Pageof 4
Human Mutation|January 1, 1995
Characterisation of molecular defects in X-linked amelogenesis imperfecta (AIH1)N J Lench, G B Winter
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|March 1, 1997
DNA diagnosis of X-linked amelogenesis imperfecta (AIH1)N J Lench, A H Brook
Human Genetics|April 1, 1997
The human gene encoding FKBP-rapamycin associated protein (FRAP) maps to chromosomal band 1p36.2N J Lench, R Macadam, A F Markham
Molecular Pathology : MP|August 26, 1998
Evidence for a common mutation in hereditary pancreatitisS M Bell, C Bennett, A F Markham, et al.
Biochimica Et Biophysica Acta|October 19, 1999
Isolation and characterisation of a cDNA encoding the precursor for a novel member of the acyl-CoA dehydrogenase gene familyE A Telford, L M Moynihan, A F Markham, et al.
Current Opinion in Biotechnology|December 1, 1994
Comparative genetic mapping for the identification of novel diagnostic and therapeutic targetsP L Coletta, N J Lench, K A Brown, et al.
Nucleic Acids Research|June 1, 1996
Vectorette PCR isolation of microsatellite repeat sequences using anchored dinucleotide repeat primersN J Lench, A Norris, A Bailey, et al.
Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics|June 1, 1995
Immunoglobulin gene rearrangements in lymphoplasmacytic infiltrates of labial salivary glands in Sjögren's syndrome. A possible predictor of lymphoma developmentR Jordan, T C Diss, N J Lench, et al.
European Journal of Human Genetics : EJHG|February 15, 2001
Maternally inherited hearing impairment in a family with the mitochondrial DNA A7445G mutationT P Hutchin, N J Lench, S Arbuzova, et al.
International Journal of Radiation Biology|December 1, 1994
DNA marker D11S384 shows zero recombination with the ataxia-telangiectasia locus in North American familiesN J Lench, P Athma, A Ottaiano, et al.
Pageof 4