Gal A - Search Results

1

Assignment of a gene for autosomal recessive retinitis pigmentosa (RP12) to chromosome 1q31-q32.1 in an inbred and genetically heterogeneous disease population.

van Soest S, van den Born LI, Gal A, Farrar GJ, Bleeker-Wagemakers LM, Westerveld A, Humphries P, Sandkuijl LA, Bergen AA. van Soest S, et al. Among authors: gal a. Genomics. 1994 Aug;22(3):499-504. doi: 10.1006/geno.1994.1422. Genomics. 1994. PMID: 8001962

2

Evidence for nonallelic genetic heterogeneity in autosomal recessive retinitis pigmentosa.

Bleeker-Wagemakers LM, Gal A, Kumar-Singh R, van den Born LI, Li Y, Schwinger E, Sandkuijl LA, Bergen AA, Kenna P, Humphries P, et al. Bleeker-Wagemakers LM, et al. Among authors: gal a. Genomics. 1992 Nov;14(3):811-2. doi: 10.1016/s0888-7543(05)80195-8. Genomics. 1992. PMID: 1427914

3

Localization of the X-linked ocular albinism gene (OA1) between DXS278/DXS237 and DXS143/DXS16 by linkage analysis.

Bergen AA, Samanns C, Van Dorp DB, Ferguson-Smith MA, Gal A, Bleeker-Wagemakers EM. Bergen AA, et al. Among authors: gal a. Ophthalmic Paediatr Genet. 1990 Sep;11(3):165-70. doi: 10.3109/13816819009020975. Ophthalmic Paediatr Genet. 1990. PMID: 2280973

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

Thr4Lys rhodopsin mutation is associated with autosomal dominant retinitis pigmentosa of the cone-rod type in a small Dutch family.

van den Born LI, van Schooneveld MJ, de Jong LA, Riemslag FC, de Jong PT, Gal A, Bleeker-Wagemakers EM. van den Born LI, et al. Among authors: gal a. Ophthalmic Genet. 1994 Jun;15(2):51-60. doi: 10.3109/13816819409098864. Ophthalmic Genet. 1994. PMID: 7850269

6

Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8).

Kumar-Singh R, Farrar GJ, Mansergh F, Kenna P, Bhattacharya S, Gal A, Humphries P. Kumar-Singh R, et al. Among authors: gal a. Hum Mol Genet. 1993 Jul;2(7):875-8. doi: 10.1093/hmg/2.7.875. Hum Mol Genet. 1993. PMID: 8364569

7

Multipoint linkage analysis in X-linked juvenile retinoschisis.

Bergen AA, van Schooneveld MJ, Orth U, Bleeker-Wagemakers EM, Gal A. Bergen AA, et al. Among authors: gal a. Clin Genet. 1993 Mar;43(3):113-6. doi: 10.1111/j.1399-0004.1993.tb04433.x. Clin Genet. 1993. PMID: 8500256

8

Carrier detection in X-linked ocular albinism of the Nettleship-Falls type by DNA analysis.

Bergen AA, Schuurman EJ, van den Born LI, Samanns C, van Dorp DB, Pinckers AJ, Bakker E, van Ommen GJ, Gal A, Bleeker-Wagemakers EM. Bergen AA, et al. Among authors: gal a. Clin Genet. 1992 Mar;41(3):135-8. doi: 10.1111/j.1399-0004.1992.tb03649.x. Clin Genet. 1992. PMID: 1348665

9

Multipoint linkage analysis in X-linked ocular albinism of the Nettleship-Falls type.

Bergen AA, Samanns C, Schuurman EJ, van Osch L, van Dorp DB, Pinckers AJ, Bakker E, Gal A, van Ommen GJ, Bleeker-Wagemakers EM. Bergen AA, et al. Among authors: gal a. Hum Genet. 1991 Dec;88(2):162-6. doi: 10.1007/BF00206065. Hum Genet. 1991. PMID: 1684563

10

Localizing multiple X chromosome-linked retinitis pigmentosa loci using multilocus homogeneity tests.

Ott J, Bhattacharya S, Chen JD, Denton MJ, Donald J, Dubay C, Farrar GJ, Fishman GA, Frey D, Gal A, et al. Ott J, et al. Among authors: gal a. Proc Natl Acad Sci U S A. 1990 Jan;87(2):701-4. doi: 10.1073/pnas.87.2.701. Proc Natl Acad Sci U S A. 1990. PMID: 2300556 Free PMC article.

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