Search research articles
Contact Us
Filters
Showing results (151-160 of 168) with videos related to
Page
of 17
Sort By:
Journal of Medical Genetics
|
September 1, 1995
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosa
M G Dunnill, C H Rodeck, A J Richards, et al.
The British Journal of Dermatology
|
May 30, 2019
Electron microscopy in the diagnosis of Ehlers-Danlos syndromes: correlation with clinical and genetic investigations
C Angwin, N Ghali, D Baker, et al.
The Journal of Biological Chemistry
|
October 15, 1988
Substitution of cysteine for glycine within the carboxyl-terminal telopeptide of the alpha 1 chain of type I collagen produces mild osteogenesis imperfecta
D H Cohn, S Apone, D R Eyre, et al.
Journal of Medical Genetics
|
February 1, 1990
Linkage data for Marfan syndrome and markers on chromosomes 1 and 11
J de Groote, P A Farndon, M V Kilpatrick, et al.
Journal of Medical Genetics
|
October 1, 1994
Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities
M G Dunnill, A J Richards, G Milana, et al.
Clinical and Experimental Dermatology
|
January 1, 1984
The prevalence of bone cysts in Darier's disease: a survey of 31 cases
A J Crisp, C M Payne, J Adams, et al.
The British Journal of Dermatology
|
April 1, 1996
First trimester DNA-based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus sampling
J A McGrath, M G Dunnill, A M Christiano, et al.
The British Journal of Dermatology
|
November 28, 2002
Severe panniculitis caused by homozygous ZZ alpha1-antitrypsin deficiency treated successfully with human purified enzyme (Prolastin)
M M U Chowdhury, E J Williams, J S Morris, et al.
Journal of Medical Genetics
|
February 1, 1990
An exclusion map of Marfan syndrome
S H Blanton, M Sarfarazi, H Eiberg, et al.
Clinical Genetics
|
March 1, 1989
Phenotypical features of an unique Irish family with severe autosomal recessive osteogenesis imperfecta
E M Williams, A C Nicholls, S C Daw, et al.
Page
of 17
Search research articles
Search
Showing results (151-160 of 168) with videos related to
Sort By:
Page
of 17
Journal of Medical Genetics
|
September 1, 1995
Use of type VII collagen gene (COL7A1) markers in prenatal diagnosis of recessive dystrophic epidermolysis bullosa
M G Dunnill, C H Rodeck, A J Richards, et al.
The British Journal of Dermatology
|
May 30, 2019
Electron microscopy in the diagnosis of Ehlers-Danlos syndromes: correlation with clinical and genetic investigations
C Angwin, N Ghali, D Baker, et al.
The Journal of Biological Chemistry
|
October 15, 1988
Substitution of cysteine for glycine within the carboxyl-terminal telopeptide of the alpha 1 chain of type I collagen produces mild osteogenesis imperfecta
D H Cohn, S Apone, D R Eyre, et al.
Journal of Medical Genetics
|
February 1, 1990
Linkage data for Marfan syndrome and markers on chromosomes 1 and 11
J de Groote, P A Farndon, M V Kilpatrick, et al.
Journal of Medical Genetics
|
October 1, 1994
Genetic linkage to the type VII collagen gene (COL7A1) in 26 families with generalised recessive dystrophic epidermolysis bullosa and anchoring fibril abnormalities
M G Dunnill, A J Richards, G Milana, et al.
Clinical and Experimental Dermatology
|
January 1, 1984
The prevalence of bone cysts in Darier's disease: a survey of 31 cases
A J Crisp, C M Payne, J Adams, et al.
The British Journal of Dermatology
|
April 1, 1996
First trimester DNA-based exclusion of recessive dystrophic epidermolysis bullosa from chorionic villus sampling
J A McGrath, M G Dunnill, A M Christiano, et al.
The British Journal of Dermatology
|
November 28, 2002
Severe panniculitis caused by homozygous ZZ alpha1-antitrypsin deficiency treated successfully with human purified enzyme (Prolastin)
M M U Chowdhury, E J Williams, J S Morris, et al.
Journal of Medical Genetics
|
February 1, 1990
An exclusion map of Marfan syndrome
S H Blanton, M Sarfarazi, H Eiberg, et al.
Clinical Genetics
|
March 1, 1989
Phenotypical features of an unique Irish family with severe autosomal recessive osteogenesis imperfecta
E M Williams, A C Nicholls, S C Daw, et al.
Page
of 17