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F M Pope

Showing results (141-150 of 168) with videos related to

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The British Journal of Dermatology|July 1, 1987
Ehlers-Danlos syndrome type I: a clinical and ultrastructural study of a family with reduced amounts of collagen type IIIA De Paepe, A Nicholls, P Narcisi, et al.
The British Journal of Ophthalmology|March 24, 2000
COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromesA J Richards, S Martin, J R Yates, et al.
Birth Defects Original Article Series|January 1, 1975
The molecular bases of certain inherited diseases of connective tissues involving collagenG R Martin, J R Lichtenstein, V A McKusick, et al.
Human Genetics|January 1, 1992
A 27-bp deletion from one allele of the type III collagen gene (COL3A1) in a large family with Ehlers-Danlos syndrome type IVA J Richards, J C Lloyd, P Narcisi, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|October 1, 1992
Ehlers Danlos syndrome type I with novel dental featuresF M Pope, A Komorowska, K W Lee, et al.
Journal of the American Academy of Dermatology|January 1, 1994
Classification of pseudoxanthoma elasticum: report of a consensus conferenceM Lebwohl, K Neldner, F M Pope, et al.
American Journal of Human Genetics|February 1, 1990
Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2B Sykes, D Ogilvie, P Wordsworth, et al.
American Journal of Medical Genetics|February 15, 1992
Molecular nosology of heritable disorders of connective tissueP Beighton, A De Paepe, J G Hall, et al.
The British Journal of Ophthalmology|May 1, 1981
Angioid streaks in Jamaican patients with homozygous sickle cell diseaseA M Hamilton, F M Pope, P I Condon, et al.
Eye (London, England)|January 1, 1994
Stickler syndrome: correlation between vitreoretinal phenotypes and linkage to COL 2A1M P Snead, S J Payne, D E Barton, et al.
Pageof 17

Showing results (141-150 of 168) with videos related to

Sort By:
Pageof 17
The British Journal of Dermatology|July 1, 1987
Ehlers-Danlos syndrome type I: a clinical and ultrastructural study of a family with reduced amounts of collagen type IIIA De Paepe, A Nicholls, P Narcisi, et al.
The British Journal of Ophthalmology|March 24, 2000
COL2A1 exon 2 mutations: relevance to the Stickler and Wagner syndromesA J Richards, S Martin, J R Yates, et al.
Birth Defects Original Article Series|January 1, 1975
The molecular bases of certain inherited diseases of connective tissues involving collagenG R Martin, J R Lichtenstein, V A McKusick, et al.
Human Genetics|January 1, 1992
A 27-bp deletion from one allele of the type III collagen gene (COL3A1) in a large family with Ehlers-Danlos syndrome type IVA J Richards, J C Lloyd, P Narcisi, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|October 1, 1992
Ehlers Danlos syndrome type I with novel dental featuresF M Pope, A Komorowska, K W Lee, et al.
Journal of the American Academy of Dermatology|January 1, 1994
Classification of pseudoxanthoma elasticum: report of a consensus conferenceM Lebwohl, K Neldner, F M Pope, et al.
American Journal of Human Genetics|February 1, 1990
Consistent linkage of dominantly inherited osteogenesis imperfecta to the type I collagen loci: COL1A1 and COL1A2B Sykes, D Ogilvie, P Wordsworth, et al.
American Journal of Medical Genetics|February 15, 1992
Molecular nosology of heritable disorders of connective tissueP Beighton, A De Paepe, J G Hall, et al.
The British Journal of Ophthalmology|May 1, 1981
Angioid streaks in Jamaican patients with homozygous sickle cell diseaseA M Hamilton, F M Pope, P I Condon, et al.
Eye (London, England)|January 1, 1994
Stickler syndrome: correlation between vitreoretinal phenotypes and linkage to COL 2A1M P Snead, S J Payne, D E Barton, et al.
Pageof 17