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N V Whittock

Showing results (1-10 of 19) with videos related to

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Clinical and Experimental Dermatology|June 26, 2003
Targetting of desmoglein 1 in inherited and acquired skin diseasesN V Whittock, C Bower
Biochemical and Biophysical Research Communications|February 22, 2001
Genomic organization, amplification, fine mapping, and intragenic polymorphisms of the human hemidesmosomal tetraspanin CD151 geneN V Whittock, W H McLean
Experimental Dermatology|October 4, 2000
Genomic organization and amplification of the human plakoglobin gene (JUP)N V Whittock, R A Eady, J A McGrath
Biochemical and Biophysical Research Communications|January 7, 2000
Genomic organization and amplification of the human keratin 15 and keratin 19 genesN V Whittock, R A Eady, J A McGrath
Biochemical and Biophysical Research Communications|July 25, 2000
Genomic organization and amplification of the human epidermal type II keratin genes K1 and K5N V Whittock, R A Eady, J A McGrath
Genetic Testing|January 1, 1997
Dystrophin point mutation screening using a multiplexed protein truncation testN V Whittock, R G Roberts, C G Mathew, et al.
Prenatal Diagnosis|September 17, 2003
Molecular prenatal diagnosis in a case of an X-linked dominant chondrodysplasia punctataN V Whittock, L Izatt, S L Simpson-Dent, et al.
The British Journal of Dermatology|September 5, 2001
New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of SiemensN V Whittock, G H Ashton, W A Griffiths, et al.
The Journal of Investigative Dermatology|August 22, 2000
Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia/skin fragility syndromeN V Whittock, M Haftek, N Angoulvant, et al.
The British Journal of Dermatology|February 1, 2006
Preimplantation genetic diagnosis of skin fragility-ectodermal dysplasia syndromeH Fassihi, J Grace, A Lashwood, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Clinical and Experimental Dermatology|June 26, 2003
Targetting of desmoglein 1 in inherited and acquired skin diseasesN V Whittock, C Bower
Biochemical and Biophysical Research Communications|February 22, 2001
Genomic organization, amplification, fine mapping, and intragenic polymorphisms of the human hemidesmosomal tetraspanin CD151 geneN V Whittock, W H McLean
Experimental Dermatology|October 4, 2000
Genomic organization and amplification of the human plakoglobin gene (JUP)N V Whittock, R A Eady, J A McGrath
Biochemical and Biophysical Research Communications|January 7, 2000
Genomic organization and amplification of the human keratin 15 and keratin 19 genesN V Whittock, R A Eady, J A McGrath
Biochemical and Biophysical Research Communications|July 25, 2000
Genomic organization and amplification of the human epidermal type II keratin genes K1 and K5N V Whittock, R A Eady, J A McGrath
Genetic Testing|January 1, 1997
Dystrophin point mutation screening using a multiplexed protein truncation testN V Whittock, R G Roberts, C G Mathew, et al.
Prenatal Diagnosis|September 17, 2003
Molecular prenatal diagnosis in a case of an X-linked dominant chondrodysplasia punctataN V Whittock, L Izatt, S L Simpson-Dent, et al.
The British Journal of Dermatology|September 5, 2001
New mutations in keratin 1 that cause bullous congenital ichthyosiform erythroderma and keratin 2e that cause ichthyosis bullosa of SiemensN V Whittock, G H Ashton, W A Griffiths, et al.
The Journal of Investigative Dermatology|August 22, 2000
Genomic amplification of the human plakophilin 1 gene and detection of a new mutation in ectodermal dysplasia/skin fragility syndromeN V Whittock, M Haftek, N Angoulvant, et al.
The British Journal of Dermatology|February 1, 2006
Preimplantation genetic diagnosis of skin fragility-ectodermal dysplasia syndromeH Fassihi, J Grace, A Lashwood, et al.
Pageof 2