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P Beighton

Showing results (251-260 of 292) with videos related to

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The British Journal of Radiology|June 1, 1979
The radiological manifestations of metaphyseal dysplasia (Pyle disease)N G Heselson, M S Raad, H Hamersma, et al.
Clinical Genetics|April 1, 1983
The fragile X chromosome in a large Indian kindredR J Gardner, R D Smart, J M Cornell, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 26, 1985
Ectrodactyly in central AfricaD Viljoen, H M Farrell, J J Brossy, et al.
American Journal of Human Genetics|October 1, 1995
Fine localization of the locus for autosomal dominant retinitis pigmentosa on chromosome 17pR Goliath, Y Shugart, P Janssens, et al.
American Journal of Human Genetics|November 1, 1992
Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldismR A Spritz, S A Holmes, R Ramesar, et al.
American Journal of Medical Genetics|June 1, 1989
Two rare developmental defects of the lower limbs with confirmation of the Lewin and Opitz hypothesis on the fibular and tibial developmental fieldsL Pavone, D Viljoen, S Ardito, et al.
American Journal of Medical Genetics|October 1, 1990
Spondyloepiphyseal dysplasia, mild autosomal dominant type is not due to primary defects of type II collagenI J Anderson, P Tsipouras, C Scher, 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.
Journal of Medical Genetics|June 1, 1996
Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneityR S Ramesar, J Greenberg, R Martin, et al.
American Journal of Human Genetics|March 3, 1999
Autosomal dominant (Beukes) premature degenerative osteoarthropathy of the hip joint maps to an 11-cM region on chromosome 4q35P Roby, S Eyre, J Worthington, et al.
Pageof 30

Showing results (251-260 of 292) with videos related to

Sort By:
Pageof 30
The British Journal of Radiology|June 1, 1979
The radiological manifestations of metaphyseal dysplasia (Pyle disease)N G Heselson, M S Raad, H Hamersma, et al.
Clinical Genetics|April 1, 1983
The fragile X chromosome in a large Indian kindredR J Gardner, R D Smart, J M Cornell, et al.
South African Medical Journal = Suid-Afrikaanse Tydskrif Vir Geneeskunde|October 26, 1985
Ectrodactyly in central AfricaD Viljoen, H M Farrell, J J Brossy, et al.
American Journal of Human Genetics|October 1, 1995
Fine localization of the locus for autosomal dominant retinitis pigmentosa on chromosome 17pR Goliath, Y Shugart, P Janssens, et al.
American Journal of Human Genetics|November 1, 1992
Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldismR A Spritz, S A Holmes, R Ramesar, et al.
American Journal of Medical Genetics|June 1, 1989
Two rare developmental defects of the lower limbs with confirmation of the Lewin and Opitz hypothesis on the fibular and tibial developmental fieldsL Pavone, D Viljoen, S Ardito, et al.
American Journal of Medical Genetics|October 1, 1990
Spondyloepiphyseal dysplasia, mild autosomal dominant type is not due to primary defects of type II collagenI J Anderson, P Tsipouras, C Scher, 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.
Journal of Medical Genetics|June 1, 1996
Mapping of the gene for cleidocranial dysplasia in the historical Cape Town (Arnold) kindred and evidence for locus homogeneityR S Ramesar, J Greenberg, R Martin, et al.
American Journal of Human Genetics|March 3, 1999
Autosomal dominant (Beukes) premature degenerative osteoarthropathy of the hip joint maps to an 11-cM region on chromosome 4q35P Roby, S Eyre, J Worthington, et al.
Pageof 30