-
1
-
-
0006902140
-
Glaucoma in infants and children
-
Nelson LB, Calhoun JH, Robinson DHWB (eds): Philadelphia, Saunders
-
Walton DS: Glaucoma in infants and children; in Nelson LB, Calhoun JH, Robinson DHWB (eds): Pediatric Ophthalmology, ed 3. Philadelphia, Saunders, 1991.
-
(1991)
Pediatric Ophthalmology, Ed 3
-
-
Walton, D.S.1
-
2
-
-
0019291895
-
Congenital glaucoma and its inheritance
-
François J: Congenital glaucoma and its inheritance. Ophthalmologica 1972;181:61-73.
-
(1972)
Ophthalmologica
, vol.181
, pp. 61-73
-
-
François, J.1
-
3
-
-
0003116189
-
Care of the infantile glaucoma patient
-
Reineck RD (ed): New York, Raven Press
-
Jaffar MS: Care of the infantile glaucoma patient; in Reineck RD (ed): Ophthalmol Annual, New York, Raven Press, 1988, p 15.
-
(1988)
Ophthalmol Annual
, pp. 15
-
-
Jaffar, M.S.1
-
4
-
-
0018831303
-
Genetic heterogeneity of congenital glaucoma
-
Genčík A, Genčíková A, Gerinec A: Genetic heterogeneity of congenital glaucoma. Clin Genet 1980;17:241-248.
-
(1980)
Clin Genet
, vol.17
, pp. 241-248
-
-
Genčík, A.1
Genčíková, A.2
Gerinec, A.3
-
5
-
-
0020071174
-
Congenital glaucoma in Gypsies from Slovakia
-
Genčíková A, Genčík A: Congenital glaucoma in Gypsies from Slovakia. Hum Hered 1982;32:270-273.
-
(1982)
Hum Hered
, vol.32
, pp. 270-273
-
-
Genčíková, A.1
Genčík, A.2
-
6
-
-
0024388554
-
Epidemiology and genetics of primary congenital glaucoma in Slovakia, Description of a form of primary congenital glaucoma m gypsies with autosomal-recessive inheritance and complete penetrance
-
Genčík A: Epidemiology and genetics of primary congenital glaucoma in Slovakia, Description of a form of primary congenital glaucoma m gypsies with autosomal-recessive inheritance and complete penetrance. Dev Ophthalmol 1989;16:76-115.
-
(1989)
Dev Ophthalmol
, vol.16
, pp. 76-115
-
-
Genčík, A.1
-
7
-
-
0028880039
-
Assignment of a locus (GLC3A) for primary congenital glaucoma (buphthalmos) to 2p21 and evidence for genetic heterogeneity
-
Sarfarazi M, Akarsu AN, Hossain A, Turacli ME, Aktan SG, Barsoum-Homsy M, Chevrette L, Sayli BS: Assignment of a locus (GLC3A) for primary congenital glaucoma (buphthalmos) to 2p21 and evidence for genetic heterogeneity. Genomics 1995;30:171-177.
-
(1995)
Genomics
, vol.30
, pp. 171-177
-
-
Sarfarazi, M.1
Akarsu, A.N.2
Hossain, A.3
Turacli, M.E.4
Aktan, S.G.5
Barsoum-Homsy, M.6
Chevrette, L.7
Sayli, B.S.8
-
8
-
-
0029836678
-
A second locus (GLC3B) for primary congenital glaucoma (buphthalmos) maps to the 1p36 region
-
Akarsu AN, Turacli ME, Aktan SG, Barsoum-Homsy M, Chevrette L, Sayli BS, Sarfarazi M: A second locus (GLC3B) for primary congenital glaucoma (buphthalmos) maps to the 1p36 region. Hum Mol Genet 1996;5:1199-1203.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1199-1203
-
-
Akarsu, A.N.1
Turacli, M.E.2
Aktan, S.G.3
Barsoum-Homsy, M.4
Chevrette, L.5
Sayli, B.S.6
Sarfarazi, M.7
-
9
-
-
6844225883
-
Mapping strategies in primary congenital glaucoma (PGC)
-
Bejjani BA, Anderson KL, Lewis RA, Tomey KF, Astle WF, Dueker DK, Karcioglu ZA, Otterud B, Leppert M, Lupski JR: Mapping strategies in primary congenital glaucoma (PGC). Am J Hum Genet 1996; 59(suppl):A212/1216.
-
(1996)
Am J Hum Genet
, vol.59
, Issue.SUPPL.
-
-
Bejjani, B.A.1
Anderson, K.L.2
Lewis, R.A.3
Tomey, K.F.4
Astle, W.F.5
Dueker, D.K.6
Karcioglu, Z.A.7
Otterud, B.8
Leppert, M.9
Lupski, J.R.10
-
10
-
-
0030942553
-
Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (buphthalmos) in families linked to the GLC3A locus on chromosome 2p21
-
Stoilov I, Akarsu AN, Sarfarazi M: Identification of three different truncating mutations in cytochrome P4501B1 (CYP1B1) as the principal cause of primary congenital glaucoma (buphthalmos) in families linked to the GLC3A locus on chromosome 2p21. Hum Mol Genet 1997;6:641-647.
-
(1997)
Hum Mol Genet
, vol.6
, pp. 641-647
-
-
Stoilov, I.1
Akarsu, A.N.2
Sarfarazi, M.3
-
11
-
-
0028931597
-
Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome
-
Dubovsky J, Sheffield VC, Duyk GM, Weber JL: Sets of short tandem repeat polymorphisms for efficient linkage screening of the human genome. Hum Mol Genet 1995;4: 449-452.
-
(1995)
Hum Mol Genet
, vol.4
, pp. 449-452
-
-
Dubovsky, J.1
Sheffield, V.C.2
Duyk, G.M.3
Weber, J.L.4
-
12
-
-
0027942568
-
A comprehensive human linkage map with centimorgan density
-
Murray JC, Buetow KH, Weber JL, Ludwigsen S, Scherpbier-Heddema T, Manion F, Quillen J, Scheffield VC, Sunden S, Duyk GM, Weissenbach J, Gyapay G, Dib C: A comprehensive human linkage map with centimorgan density. Science 1994; 265:2049-2054.
-
(1994)
Science
, vol.265
, pp. 2049-2054
-
-
Murray, J.C.1
Buetow, K.H.2
Weber, J.L.3
Ludwigsen, S.4
Scherpbier-Heddema, T.5
Manion, F.6
Quillen, J.7
Scheffield, V.C.8
Sunden, S.9
Duyk, G.M.10
Weissenbach, J.11
Gyapay, G.12
Dib, C.13
-
13
-
-
13344259999
-
The Généthon human genetic linkage map
-
Dib C, Faure S, Fizames C, Samson D, Drouot N, Vignal A, Millasseau P: The Généthon human genetic linkage map. Nature 1996;380:152-154.
-
(1996)
Nature
, vol.380
, pp. 152-154
-
-
Dib, C.1
Faure, S.2
Fizames, C.3
Samson, D.4
Drouot, N.5
Vignal, A.6
Millasseau, P.7
-
15
-
-
6844244462
-
Linkage analysis and family classification under heterogeneity
-
Ott J: Linkage analysis and family classification under heterogeneity. Ann Hum Genet 1983;6:415-419.
-
(1983)
Ann Hum Genet
, vol.6
, pp. 415-419
-
-
Ott, J.1
-
16
-
-
0023286166
-
Slovak Roms (Gypsies): Population with the highest coefficient of inbreeding in Europe
-
Ferák V, Sieglová Z, Siváková D: Slovak Roms (Gypsies): Population with the highest coefficient of inbreeding in Europe. Bratislavské lekárske listy 1987;87:168-175.
-
(1987)
Bratislavské Lekárske Listy
, vol.87
, pp. 168-175
-
-
Ferák, V.1
Sieglová, Z.2
Siváková, D.3
-
17
-
-
0020000365
-
Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effect
-
Ferák V, Genčíková A, Genčík A: Population genetic aspects of primary congenital glaucoma. II. Fitness, parental consanguinity, founder effect. Hum Genet 1982;61:198-200.
-
(1982)
Hum Genet
, vol.61
, pp. 198-200
-
-
Ferák, V.1
Genčíková, A.2
Genčík, A.3
|