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1.2 Population genetics (16)

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5151 Are optic disc drusen inherited?
Antcliff RJ; Spalton DJ
Ophthalmology 1999; 106: 1278-1281
5152 X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28
Armfield K; Nelson R; Lubs HA; Hane B; Schroer RJ; Arena F; Schwartz CE; Stevenson RE
American Journal of Medical Genetics 1999; 85: 236-242
5153 Family history of glaucoma in the primary and secondary open-angle glaucomas
Budde WM; Jonas JB
Graefe's Archive for Clinical and Experimental Ophthalmology 1999; 237: 554-557
5154 Glaucoma genetics: Where are we? where will we go?
Craig JE; Mackey DA
Current Opinions in Ophthalmology 1999; 10: 126-134
5155 Analysis of myocilin mutations in 1703 glaucoma patients from five different populations.
Fingert JH; Heon E; Liebmann JM; Yamamoto T; Craig J; Rait J; Kawase K; Hoh ST; Buys YM; Dickinson J
Human Molecular Genetics 1999; 8: 899-905
5156 Mutational analysis of PAX6: 16 novel mutations including 5 missense mutations with a mild aniridia phenotype
Gronskov K; Rosenberg T; Sand A; Brondum-Nielsen K
European Journal of Human Genetics 1999; 7: 274-286
5157 Family history and some other factors in primary open angle glaucoma.
Konareva-Kostianeva M
Folia Medica 1998; 40: 78-81
5158 Dominant inheritance of chronic open-angle glaucoma in an Algerian family
Ouhadj O; Degheb N; Nouri MT
Journal Français d'Ophtalmologie 1999; 22: 571-576
5159 Identification of a single ancestral CYP1B1 mutation in Slovak Gypsies (Roms) affected with primary congenital glaucoma.
Plasilova M; Stoilov I; Sarfarazi M; Kadasi L; Ferakova E; Ferak V
Journal of Medical Genetics 1999; 36: 290-294
5160 The inheritance of the pigment dispersion syndrome in blacks
Roberts DK; Meetz RE; Chaglasian MA
Journal of Glaucoma 1999; 8: 250-256
5161 A novel gene (oculomedin) induced by mechanical stretching in human trabecular cells of the eye
Sato Y; Matsuo T; Ohtsuki H
Biochemical and Biophysical Research Communications 1999; 259: 349-351
5162 Expression pattern and in situ localization of the mouse homologue of the human MYOC (GLC1A) gene in adult brain.
Swiderski RE; Ying L; Cassell MD; Alward WL; Stone EM; Sheffield VC
Molecular Brain Research 1999; 68: 64-72
5163 Clinical phenotype of a Japanese family with primary open angle glaucoma caused by a Pro370Leu mutation in the MYOC/TIGR gene.
Taniguchi F; Suzuki Y; Shirato S; Ohta S
Japanese Journal of Ophthalmology 1999; 43: 80-84
5164 Detection of a new TIGR gene mutation in a Japanese family with primary open angle glaucoma.
Yokoyama A; Nao-i N; Date Y; Nakazato M; Chumann H; Chihara E; Sawada A; Matsukura S
Japanese Journal of Ophthalmology 1999; 43: 85-88
5165 Mutations of the TIGR/MYOC gene in primary open-angle glaucoma in Korea (letter)
Yoon SJ; Kim HS; Moon JI; Lim JM; Joo CK
American Journal of Human Genetics 1999; 64: 1775-1778
5166 Discordance of primary infantile glaucoma in monozygotic twins
Zhang K; Jampel HD
American Journal of Ophthalmology 1999; 128: 97-98

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