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American Journal of Human Genetics
|
April 1, 1997
Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors
A H Prowse, A R Webster, F M Richards, et al.
Genomics
|
February 15, 1997
Chromosomal assignment of 311 sequences transcribed in human adult testis
M H Jones, Y Zhang, K N Tirosvoutis, et al.
Eye (London, England)
|
June 27, 2015
Diverse clinical phenotypes associated with a nonsense mutation in FAM161A
A M Rose, P Sergouniotis, G Alfano, et al.
The British Journal of Ophthalmology
|
February 22, 2005
A detailed phenotypic study of "cone dystrophy with supernormal rod ERG"
M Michaelides, G E Holder, A R Webster, et al.
The British Journal of Ophthalmology
|
October 27, 2007
Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophy
A G Robson, M Michaelides, V A Luong, et al.
The British Journal of Ophthalmology
|
May 23, 2006
Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene
M Tschernutter, S A Jenkins, N H Waseem, et al.
Molecular Vision
|
June 19, 2009
Clinical and biochemical effects of the E139K missense mutation in the TIMP3 gene, associated with Sorsby fundus dystrophy
Z Saihan, Z Li, J Rice, et al.
The British Journal of Ophthalmology
|
November 21, 2007
ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy
M Michaelides, L L Chen, M A Brantley, et al.
Experimental Eye Research
|
April 20, 2001
Spectrum of mutations in USH2A in British patients with Usher syndrome type II
B P Leroy, J A Aragon-Martin, M D Weston, et al.
Journal of Medical Genetics
|
November 17, 2007
A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts
A Arora, P J Minogue, X Liu, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 45) with videos related to
Sort By:
Page
of 5
American Journal of Human Genetics
|
April 1, 1997
Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors
A H Prowse, A R Webster, F M Richards, et al.
Genomics
|
February 15, 1997
Chromosomal assignment of 311 sequences transcribed in human adult testis
M H Jones, Y Zhang, K N Tirosvoutis, et al.
Eye (London, England)
|
June 27, 2015
Diverse clinical phenotypes associated with a nonsense mutation in FAM161A
A M Rose, P Sergouniotis, G Alfano, et al.
The British Journal of Ophthalmology
|
February 22, 2005
A detailed phenotypic study of "cone dystrophy with supernormal rod ERG"
M Michaelides, G E Holder, A R Webster, et al.
The British Journal of Ophthalmology
|
October 27, 2007
Functional correlates of fundus autofluorescence abnormalities in patients with RPGR or RIMS1 mutations causing cone or cone rod dystrophy
A G Robson, M Michaelides, V A Luong, et al.
The British Journal of Ophthalmology
|
May 23, 2006
Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene
M Tschernutter, S A Jenkins, N H Waseem, et al.
Molecular Vision
|
June 19, 2009
Clinical and biochemical effects of the E139K missense mutation in the TIMP3 gene, associated with Sorsby fundus dystrophy
Z Saihan, Z Li, J Rice, et al.
The British Journal of Ophthalmology
|
November 21, 2007
ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy
M Michaelides, L L Chen, M A Brantley, et al.
Experimental Eye Research
|
April 20, 2001
Spectrum of mutations in USH2A in British patients with Usher syndrome type II
B P Leroy, J A Aragon-Martin, M D Weston, et al.
Journal of Medical Genetics
|
November 17, 2007
A novel connexin50 mutation associated with congenital nuclear pulverulent cataracts
A Arora, P J Minogue, X Liu, et al.
Page
of 5