Gal A - Search Results

1

Genetic mapping of RP1 on 8q11-q21 in an Australian family with autosomal dominant retinitis pigmentosa reduces the critical region to 4 cM between D8S601 and D8S285.

Xu SY, Denton M, Sullivan L, Daiger SP, Gal A. Xu SY, et al. Among authors: gal a. Hum Genet. 1996 Dec;98(6):741-3. doi: 10.1007/s004390050296. Hum Genet. 1996. PMID: 8931712

2

No evidence of linkage between the locus for autosomal dominant retinitis pigmentosa and D3S47 (C17) in three Australian families.

Jiménez JB, Samanns C, Watty A, Pongratz J, Olsson JE, Dickinson P, Buttery R, Gal A, Denton MJ. Jiménez JB, et al. Among authors: gal a. Hum Genet. 1991 Jan;86(3):265-7. doi: 10.1007/BF00202406. Hum Genet. 1991. PMID: 1997379

3

Two different genes for X-linked retinitis pigmentosa.

Wirth B, Denton MJ, Chen JD, Neugebauer M, Halliday FB, van Schooneveld M, Donald J, Bleeker-Wagemakers EM, Pearson PL, Gal A. Wirth B, et al. Among authors: gal a. Genomics. 1988 Apr;2(3):263-6. doi: 10.1016/0888-7543(88)90011-0. Genomics. 1988. PMID: 3397063

4

Autosomal recessive retinitis pigmentosa locus maps on chromosome 1q in a large consanguineous family from Pakistan.

Leutelt J, Oehlmann R, Younus F, van den Born LI, Weber JL, Denton MJ, Mehdi SQ, Gal A. Leutelt J, et al. Among authors: gal a. Clin Genet. 1995 Mar;47(3):122-4. doi: 10.1111/j.1399-0004.1995.tb03943.x. Clin Genet. 1995. PMID: 7634534

5

Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosa.

Fuchs S, Kranich H, Denton MJ, Zrenner E, Bhattacharya SS, Humphries P, Gal A. Fuchs S, et al. Among authors: gal a. Hum Mol Genet. 1994 Jul;3(7):1203. doi: 10.1093/hmg/3.7.1203. Hum Mol Genet. 1994. PMID: 7981701 No abstract available.

6

Gene for autosomal dominant congenital stationary night blindness maps to the same region as the gene for the beta-subunit of the rod photoreceptor cGMP phosphodiesterase (PDEB) in chromosome 4p16.3.

Gal A, Xu S, Piczenik Y, Eiberg H, Duvigneau C, Schwinger E, Rosenberg T. Gal A, et al. Hum Mol Genet. 1994 Feb;3(2):323-5. doi: 10.1093/hmg/3.2.323. Hum Mol Genet. 1994. PMID: 8004102

7

Autosomal dominant 'sector' retinitis pigmentosa due to a point mutation predicting an Asn-15-Ser substitution of rhodopsin.

Kranich H, Bartkowski S, Denton MJ, Krey S, Dickinson P, Duvigneau C, Gal A. Kranich H, et al. Among authors: gal a. Hum Mol Genet. 1993 Jun;2(6):813-4. doi: 10.1093/hmg/2.6.813. Hum Mol Genet. 1993. PMID: 8353500 No abstract available.

8

Autosomal dominant retinitis pigmentosa locus on chromosome 19q in a Japanese family.

Xu S, Nakazawa M, Tamai M, Gal A. Xu S, et al. Among authors: gal a. J Med Genet. 1995 Nov;32(11):915-6. doi: 10.1136/jmg.32.11.915. J Med Genet. 1995. PMID: 8592343 Free PMC article.

9

A ninth locus (RP18) for autosomal dominant retinitis pigmentosa maps in the pericentromeric region of chromosome 1.

Xu SY, Schwartz M, Rosenberg T, Gal A. Xu SY, et al. Among authors: gal a. Hum Mol Genet. 1996 Aug;5(8):1193-7. doi: 10.1093/hmg/5.8.1193. Hum Mol Genet. 1996. PMID: 8842740

10

Dinucleotide repeat polymorphisms at D9S171 and D9S741 are identical.

Xu SY, Schürmann M, Gal A. Xu SY, et al. Among authors: gal a. Clin Genet. 1996 Dec;50(6):531-2. doi: 10.1111/j.1399-0004.1996.tb02730.x. Clin Genet. 1996. PMID: 9147891 No abstract available.

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