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Surgical Neurology
|
August 1, 1993
Giant aneurysm of internal carotid artery in a four-year-old child: a case report
N K Swamy, F M Pope, H B Coakham
Clinical and Experimental Dermatology
|
March 1, 1996
Cutis laxa complicating Ehlers-Danlos syndrome type II
L S Ostlere, F M Pope, C A Holden
Journal of Medical Genetics
|
June 1, 1977
Inheritance of Ehlers-Danlos type IV syndrome
F M Pope, G R Martin, V A McKusick
Journal of Medical Genetics
|
May 1, 1993
A T+6 to C+6 mutation in the donor splice site of COL3A1 IVS7 causes exon skipping and results in Ehlers-Danlos syndrome type IV
J Lloyd, P Narcisi, A Richards, et al.
Neuropediatrics
|
November 1, 1991
Type III collagen deficient EDS IV producing muscular hypotonia with abnormal muscle fibroblasts
A Fidziańska, Z Glinka, A Kamińska, et al.
Journal of the Royal Society of Medicine
|
January 1, 1993
Spontaneous rupture of the femoral arteries
M A Cadier, G Watkin, F M Pope, et al.
Journal of the Royal Society of Medicine
|
December 1, 1983
Molecular abnormalities of collagen: a review
F M Pope, A C Nicholls, J Dorling, et al.
Thorax
|
October 1, 1983
Emphysema and cutis laxa
L Turner-Stokes, C Turton, F M Pope, et al.
Journal of Medical Genetics
|
April 6, 2001
Homozygosity for a splice site mutation of the COL1A2 gene yields a non-functional pro(alpha)2(I) chain and an EDS/OI clinical phenotype
A C Nicholls, D Valler, S Wallis, et al.
The British Journal of Dermatology
|
April 12, 2001
The Buschke-Ollendorff syndrome presenting as familial elastic tissue naevi
S L Woodrow, F M Pope, S E Handfield-Jones
Page
of 17
Search research articles
Search
Showing results (51-60 of 168) with videos related to
Sort By:
Page
of 17
Surgical Neurology
|
August 1, 1993
Giant aneurysm of internal carotid artery in a four-year-old child: a case report
N K Swamy, F M Pope, H B Coakham
Clinical and Experimental Dermatology
|
March 1, 1996
Cutis laxa complicating Ehlers-Danlos syndrome type II
L S Ostlere, F M Pope, C A Holden
Journal of Medical Genetics
|
June 1, 1977
Inheritance of Ehlers-Danlos type IV syndrome
F M Pope, G R Martin, V A McKusick
Journal of Medical Genetics
|
May 1, 1993
A T+6 to C+6 mutation in the donor splice site of COL3A1 IVS7 causes exon skipping and results in Ehlers-Danlos syndrome type IV
J Lloyd, P Narcisi, A Richards, et al.
Neuropediatrics
|
November 1, 1991
Type III collagen deficient EDS IV producing muscular hypotonia with abnormal muscle fibroblasts
A Fidziańska, Z Glinka, A Kamińska, et al.
Journal of the Royal Society of Medicine
|
January 1, 1993
Spontaneous rupture of the femoral arteries
M A Cadier, G Watkin, F M Pope, et al.
Journal of the Royal Society of Medicine
|
December 1, 1983
Molecular abnormalities of collagen: a review
F M Pope, A C Nicholls, J Dorling, et al.
Thorax
|
October 1, 1983
Emphysema and cutis laxa
L Turner-Stokes, C Turton, F M Pope, et al.
Journal of Medical Genetics
|
April 6, 2001
Homozygosity for a splice site mutation of the COL1A2 gene yields a non-functional pro(alpha)2(I) chain and an EDS/OI clinical phenotype
A C Nicholls, D Valler, S Wallis, et al.
The British Journal of Dermatology
|
April 12, 2001
The Buschke-Ollendorff syndrome presenting as familial elastic tissue naevi
S L Woodrow, F M Pope, S E Handfield-Jones
Page
of 17