Gal A - Search Results

1

Two novel mutations in the Norrie disease gene associated with the classical ocular phenotype.

Caballero M, Veske A, Rodriguez JJ, Lugo N, Schroeder B, Hesse L, Gal A. Caballero M, et al. Among authors: gal a. Ophthalmic Genet. 1996 Dec;17(4):187-91. doi: 10.3109/13816819609057892. Ophthalmic Genet. 1996. PMID: 9010869

2

Five novel mutations in the L1CAM gene in families with X linked hydrocephalus.

Gu SM, Orth U, Veske A, Enders H, Klunder K, Schlosser M, Engel W, Schwinger E, Gal A. Gu SM, et al. Among authors: gal a. J Med Genet. 1996 Feb;33(2):103-6. doi: 10.1136/jmg.33.2.103. J Med Genet. 1996. PMID: 8929944 Free PMC article.

3

Histopathological and immunohistochemical findings associated with a null mutation in the Norrie disease gene.

Schroeder B, Hesse L, Brück W, Gal A. Schroeder B, et al. Among authors: gal a. Ophthalmic Genet. 1997 Jun;18(2):71-7. doi: 10.3109/13816819709057118. Ophthalmic Genet. 1997. PMID: 9228243

4

Norrie-Warburg syndrome: two novel mutations in patients with classical clinical phenotype.

Gal A, Veske A, Jojart G, Grammatico B, Huber B, Gu S, del Porto G, Senyi K. Gal A, et al. Acta Ophthalmol Scand Suppl. 1996;(219):13-6. doi: 10.1111/j.1600-0420.1996.tb00374.x. Acta Ophthalmol Scand Suppl. 1996. PMID: 8741107

5

A missense point mutation (Leu13Arg) of the Norrie disease gene in a large Cuban kindred with Norrie disease.

Fuchs S, Xu SY, Caballero M, Salcedo M, La O A, Wedemann H, Gal A. Fuchs S, et al. Among authors: gal a. Hum Mol Genet. 1994 Apr;3(4):655-6. doi: 10.1093/hmg/3.4.655. Hum Mol Genet. 1994. PMID: 8069314 No abstract available.

6

Autosomal recessive non-syndromic deafness locus (DFNB8) maps on chromosome 21q22 in a large consanguineous kindred from Pakistan.

Veske A, Oehlmann R, Younus F, Mohyuddin A, Müller-Myhsok B, Mehdi SQ, Gal A. Veske A, et al. Among authors: gal a. Hum Mol Genet. 1996 Jan;5(1):165-8. doi: 10.1093/hmg/5.1.165. Hum Mol Genet. 1996. PMID: 8789456

7

Microsatellite (TTCC)n polymorphism in intron 6 of the canine rod photoreceptor cGMP-gated cation channel alpha-subunit gene.

Veske A, Nilsson SE, Gal A. Veske A, et al. Among authors: gal a. Anim Genet. 1997 Oct;28(5):374-5. Anim Genet. 1997. PMID: 9363608 No abstract available.

8

Microsatellite (CA)n polymorphism in intron 2 of the canine rod photoreceptor cGMP-phosphodiesterase alpha-subunit gene.

Veske A, Nilsson SE, Gal A. Veske A, et al. Among authors: gal a. Anim Genet. 1997 Oct;28(5):380. doi: 10.1111/j.1365-2052.1997.tb03284.x. Anim Genet. 1997. PMID: 9363616 No abstract available.

9

Characterization of canine rod photoreceptor cGMP-gated cation channel alpha-subunit gene and exclusion of its involvement in the hereditary retinal dystrophy of Swedish Briards.

Veske A, Nilsson SE, Gal A. Veske A, et al. Among authors: gal a. Gene. 1997 Nov 20;202(1-2):115-9. doi: 10.1016/s0378-1119(97)00461-7. Gene. 1997. PMID: 9427553

10

Organization of the canine gene encoding the E isoform of retinal guanylate cyclase (cGC-E) and exclusion of its involvement in the inherited retinal dystrophy of the Swedish Briard and Briard-beagle dogs.

Veske A, Nilsson SE, Gal A. Veske A, et al. Among authors: gal a. Biochim Biophys Acta. 1998 Jun 24;1372(1):69-77. doi: 10.1016/s0005-2736(98)00047-9. Biochim Biophys Acta. 1998. PMID: 9651484 Free article.

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