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A C Nicholls

Showing results (51-60 of 58) with videos related to

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The Journal of Investigative Dermatology|June 1, 1996
The gene encoding collagen alpha1(V)(COL5A1) is linked to mixed Ehlers-Danlos syndrome type I/IIN P Burrows, A C Nicholls, J R Yates, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1988
Spontaneous carotid cavernous fistula in Ehlers Danlos syndromeR Fox, F M Pope, P Narcisi, et al.
American Journal of Human Genetics|July 31, 1998
A point mutation in an intronic branch site results in aberrant splicing of COL5A1 and in Ehlers-Danlos syndrome type II in two British familiesN P Burrows, A C Nicholls, A J Richards, 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.
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 imperfectaD H Cohn, S Apone, D R Eyre, et al.
Clinical Genetics|March 1, 1989
Phenotypical features of an unique Irish family with severe autosomal recessive osteogenesis imperfectaE M Williams, A C Nicholls, S C Daw, et al.
Clinical and Experimental Dermatology|September 1, 1988
Type III collagen mutations in Ehlers Danlos syndrome type IV and other related disordersF M Pope, A C Nicholls, P Narcisi, et al.
Journal of Medical Genetics|August 1, 1984
The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfectaA C Nicholls, G Osse, H G Schloon, et al.
Pageof 6

Showing results (51-60 of 58) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 58 results.
The Journal of Investigative Dermatology|June 1, 1996
The gene encoding collagen alpha1(V)(COL5A1) is linked to mixed Ehlers-Danlos syndrome type I/IIN P Burrows, A C Nicholls, J R Yates, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1988
Spontaneous carotid cavernous fistula in Ehlers Danlos syndromeR Fox, F M Pope, P Narcisi, et al.
American Journal of Human Genetics|July 31, 1998
A point mutation in an intronic branch site results in aberrant splicing of COL5A1 and in Ehlers-Danlos syndrome type II in two British familiesN P Burrows, A C Nicholls, A J Richards, 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.
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 imperfectaD H Cohn, S Apone, D R Eyre, et al.
Clinical Genetics|March 1, 1989
Phenotypical features of an unique Irish family with severe autosomal recessive osteogenesis imperfectaE M Williams, A C Nicholls, S C Daw, et al.
Clinical and Experimental Dermatology|September 1, 1988
Type III collagen mutations in Ehlers Danlos syndrome type IV and other related disordersF M Pope, A C Nicholls, P Narcisi, et al.
Journal of Medical Genetics|August 1, 1984
The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfectaA C Nicholls, G Osse, H G Schloon, et al.
Pageof 6