Gal A - Search Results

1

Norrie's disease: close linkage with genetic markers from the proximal short arm of the X chromosome.

Gal A, Stolzenberger C, Wienker T, Wieacker P, Ropers HH, Friedrich U, Bleeker-Wagemakers L, Pearson P, Warburg M. Gal A, et al. Clin Genet. 1985 Mar;27(3):282-3. doi: 10.1111/j.1399-0004.1985.tb00221.x. Clin Genet. 1985. PMID: 3857130 No abstract available.

2

X-linked retinitis pigmentosa: linkage with the centromere and a cloned DNA sequence from the proximal short arm of the X chromosome.

Friedrich U, Warburg M, Wieacker P, Wienker TF, Gal A, Ropers HH. Friedrich U, et al. Among authors: gal a. Hum Genet. 1985;71(2):93-9. doi: 10.1007/BF00283360. Hum Genet. 1985. PMID: 2995237

3

Close linkage between Norrie disease, a cloned DNA sequence from the proximal short arm, and the centromere of the X chromosome.

Bleeker-Wagemakers LM, Friedrich U, Gal A, Wienker TF, Warburg M, Ropers HH. Bleeker-Wagemakers LM, et al. Among authors: gal a. Hum Genet. 1985;71(3):211-4. doi: 10.1007/BF00284575. Hum Genet. 1985. PMID: 2998969

4

Mutations in the candidate gene for Norrie disease.

Berger W, van de Pol D, Warburg M, Gal A, Bleeker-Wagemakers L, de Silva H, Meindl A, Meitinger T, Cremers F, Ropers HH. Berger W, et al. Among authors: gal a. Hum Mol Genet. 1992 Oct;1(7):461-5. doi: 10.1093/hmg/1.7.461. Hum Mol Genet. 1992. PMID: 1307245 Review.

5

X-linked dominant Charcot-Marie-Tooth disease: suggestion of linkage with a cloned DNA sequence from the proximal Xq.

Gal A, Mücke J, Theile H, Wieacker PF, Ropers HH, Wienker TF. Gal A, et al. Hum Genet. 1985;70(1):38-42. doi: 10.1007/BF00389456. Hum Genet. 1985. PMID: 2987105

6

Norrie's disease: delineation of carriers among daughters of obligate carriers by linkage analysis.

Warburg M, Friedrich U, Bleeker-Wagemakers L, Wienker TF, Gal A, Ropers HH. Warburg M, et al. Among authors: gal a. Trans Ophthalmol Soc U K (1962). 1986;105 ( Pt 1):88-93. Trans Ophthalmol Soc U K (1962). 1986. PMID: 3459299

7

Submicroscopic interstitial deletion of the X chromosome explains a complex genetic syndrome dominated by Norrie disease.

Gal A, Wieringa B, Smeets DF, Bleeker-Wagemakers L, Ropers HH. Gal A, et al. Cytogenet Cell Genet. 1986;42(4):219-24. doi: 10.1159/000132282. Cytogenet Cell Genet. 1986. PMID: 3502689

8

Gene of X-chromosomal congenital stationary night blindness is closely linked to DXS7 on Xp.

Gal A, Schinzel A, Orth U, Fraser NA, Mollica F, Craig IW, Kruse T, Mächler M, Neugebauer M, Bleeker-Wagemakers LM. Gal A, et al. Hum Genet. 1989 Mar;81(4):315-8. doi: 10.1007/BF00283682. Hum Genet. 1989. PMID: 2564836

9

[Molecular genetic diagnosis in X chromosome-linked retinitis pigmentosa].

Hogenkamp T, Wienker TF, Majewski F, Gal A. Hogenkamp T, et al. Among authors: gal a. Klin Monbl Augenheilkd. 1987 Oct;191(4):307-9. doi: 10.1055/s-2008-1050516. Klin Monbl Augenheilkd. 1987. PMID: 2891868 German.

10

X-linked dominant hypophosphatemia is closely linked to DNA markers DXS41 and DXS43 at Xp22.

Mächler M, Frey D, Gal A, Orth U, Wienker TF, Fanconi A, Schmid W. Mächler M, et al. Among authors: gal a. Hum Genet. 1986 Jul;73(3):271-5. doi: 10.1007/BF00401243. Hum Genet. 1986. PMID: 3015771

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