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Journal of Medical Genetics
|
January 1, 1990
Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus
C F Inglehearn, S S Papiha, M Jay, et al.
Nature
|
January 20, 1977
Maternal histidine metabolism and its effect on foetal development in the mouse
H Kacser, K M Mya, M Duncker, et al.
Human Mutation
|
March 27, 1999
Identification of a 5' splice site mutation in the RPGR gene in a family with X-linked retinitis pigmentosa (RP3)
K L Dry, F D Manson, A Lennon, et al.
Clinical Genetics
|
May 1, 1993
Linkage analysis in a family with complete type congenital stationary night blindness with and without myopia
K L Dry, D B Van Dorp, M A Aldred, et al.
Progress in Retinal and Eye Research
|
October 10, 2013
Using human induced pluripotent stem cells to treat retinal disease
S Borooah, M J Phillips, B Bilican, et al.
Journal of Medical Genetics
|
April 1, 1992
Evidence for linkage disequilibrium between D16S94 and the adult onset polycystic kidney disease (PKD1) gene
S E Pound, A D Carothers, P M Pignatelli, et al.
Journal of Medical Genetics
|
August 1, 1990
Linkage studies and deletion screening in choroideremia
A F Wright, R L Nussbaum, S S Bhattacharya, et al.
Molecular Psychiatry
|
February 1, 2006
The brain-derived neurotrophic factor Val66Met polymorphism is associated with age-related change in reasoning skills
S E Harris, H Fox, A F Wright, et al.
American Journal of Medical Genetics
|
December 26, 2001
Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X-linked retinitis pigmentosa
A Yokoyama, F Maruiwa, M Hayakawa, et al.
Journal of Affective Disorders
|
March 1, 1989
Cation transport in lymphoblastoid cell lines established from bipolar manic-depressive patients
R E Banks, J F Aiton, G J Naylor, et al.
Page
of 14
Search research articles
Search
Showing results (81-90 of 137) with videos related to
Sort By:
Page
of 14
Journal of Medical Genetics
|
January 1, 1990
Linkage of internal minisatellite loci on chromosome 1 and exclusion of autosomal dominant retinitis pigmentosa proximal to rhesus
C F Inglehearn, S S Papiha, M Jay, et al.
Nature
|
January 20, 1977
Maternal histidine metabolism and its effect on foetal development in the mouse
H Kacser, K M Mya, M Duncker, et al.
Human Mutation
|
March 27, 1999
Identification of a 5' splice site mutation in the RPGR gene in a family with X-linked retinitis pigmentosa (RP3)
K L Dry, F D Manson, A Lennon, et al.
Clinical Genetics
|
May 1, 1993
Linkage analysis in a family with complete type congenital stationary night blindness with and without myopia
K L Dry, D B Van Dorp, M A Aldred, et al.
Progress in Retinal and Eye Research
|
October 10, 2013
Using human induced pluripotent stem cells to treat retinal disease
S Borooah, M J Phillips, B Bilican, et al.
Journal of Medical Genetics
|
April 1, 1992
Evidence for linkage disequilibrium between D16S94 and the adult onset polycystic kidney disease (PKD1) gene
S E Pound, A D Carothers, P M Pignatelli, et al.
Journal of Medical Genetics
|
August 1, 1990
Linkage studies and deletion screening in choroideremia
A F Wright, R L Nussbaum, S S Bhattacharya, et al.
Molecular Psychiatry
|
February 1, 2006
The brain-derived neurotrophic factor Val66Met polymorphism is associated with age-related change in reasoning skills
S E Harris, H Fox, A F Wright, et al.
American Journal of Medical Genetics
|
December 26, 2001
Three novel mutations of the RPGR gene exon ORF15 in three Japanese families with X-linked retinitis pigmentosa
A Yokoyama, F Maruiwa, M Hayakawa, et al.
Journal of Affective Disorders
|
March 1, 1989
Cation transport in lymphoblastoid cell lines established from bipolar manic-depressive patients
R E Banks, J F Aiton, G J Naylor, et al.
Page
of 14