F M Pope|A C Nicholls - JoVE Visualize

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Journal of Medical Genetics|June 1, 1992

Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IVL Nuytinck, P Narcisi, A Nicholls, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 15, 1993

The gene responsible for Werner syndrome may be a cell division "counting" geneR G Faragher, I R Kill, J A Hunter, et al.

Cardiovascular Surgery (London, England)|February 8, 2000

Emergency repair of type A aortic dissection in type IV Ehlers-Danlos syndromeR Ascione, W J Gomes, M Bates, et al.

Journal of Medical Genetics|June 1, 1992

Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locusL al-Imara, A J Richards, R A Eady, et al.

American Journal of Medical Genetics|May 15, 1993

Single base mutation that substitutes glutamic acid for glycine 1021 in the COL3A1 gene and causes Ehlers-Danlos syndrome type IVP Narcisi, Y Wu, G Tromp, et al.

Clinical and Experimental Dermatology|June 30, 2009

An atypical cutaneous presentation of vasculitis with features of Churg-Strauss syndrome, associated with anti-neutrophil cytoplasmic antibodies and anti-glomerular basement membrane antibodiesC M Gleeson, J B Levy, H T Cook, et al.

Journal of Medical Genetics|July 1, 1991

Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IVA J Richards, J C Lloyd, P N Ward, et al.

Clinical and Experimental Dermatology|October 27, 2001

Elastosis perforans serpiginosa and associated disordersR K Mehta, N P Burrows, C M Payne, et al.

Archives of Dermatology|January 1, 1979

Cutaneous histologic features in Ehlers-Danlos syndrome: study of 21 patientsV I Sulica, P H Cooper, F M Pope, et al.

Genomics|July 1, 1994

Localization of the gene (LAMA4) to chromosome 6q21 and isolation of a partial cDNA encoding a variant laminin A chainA J Richards, L al-Imara, N P Carter, et al.

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Showing results (81-90 of 119) with videos related to

Sort By:

Pageof 12

Journal of Medical Genetics|June 1, 1992

Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IVL Nuytinck, P Narcisi, A Nicholls, et al.

Proceedings of the National Academy of Sciences of the United States of America|December 15, 1993

The gene responsible for Werner syndrome may be a cell division "counting" geneR G Faragher, I R Kill, J A Hunter, et al.

Cardiovascular Surgery (London, England)|February 8, 2000

Emergency repair of type A aortic dissection in type IV Ehlers-Danlos syndromeR Ascione, W J Gomes, M Bates, et al.

Journal of Medical Genetics|June 1, 1992

Linkage of autosomal dominant dystrophic epidermolysis bullosa in three British families to the marker D3S2 close to the COL7A1 locusL al-Imara, A J Richards, R A Eady, et al.

American Journal of Medical Genetics|May 15, 1993

Single base mutation that substitutes glutamic acid for glycine 1021 in the COL3A1 gene and causes Ehlers-Danlos syndrome type IVP Narcisi, Y Wu, G Tromp, et al.

Clinical and Experimental Dermatology|June 30, 2009

An atypical cutaneous presentation of vasculitis with features of Churg-Strauss syndrome, associated with anti-neutrophil cytoplasmic antibodies and anti-glomerular basement membrane antibodiesC M Gleeson, J B Levy, H T Cook, et al.

Journal of Medical Genetics|July 1, 1991

Characterisation of a glycine to valine substitution at amino acid position 910 of the triple helical region of type III collagen in a patient with Ehlers-Danlos syndrome type IVA J Richards, J C Lloyd, P N Ward, et al.

Clinical and Experimental Dermatology|October 27, 2001

Elastosis perforans serpiginosa and associated disordersR K Mehta, N P Burrows, C M Payne, et al.

Archives of Dermatology|January 1, 1979

Cutaneous histologic features in Ehlers-Danlos syndrome: study of 21 patientsV I Sulica, P H Cooper, F M Pope, et al.

Genomics|July 1, 1994

Localization of the gene (LAMA4) to chromosome 6q21 and isolation of a partial cDNA encoding a variant laminin A chainA J Richards, L al-Imara, N P Carter, et al.

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