Gal A - Search Results

1

Choroideremia-locus maps between DXS3 and DXS11 on Xq.

Gal A, Brunsmann F, Hogenkamp D, Rüther K, Ahlert D, Wienker TF, Hammerstein W, Pawlowitzki IH. Gal A, et al. Hum Genet. 1986 Jun;73(2):123-6. doi: 10.1007/BF00291600. Hum Genet. 1986. PMID: 3755117

2

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

3

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

4

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

5

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

6

Three cases of 45,X/46,XYnf mosaicism. Molecular analysis revealed heterogeneity of the nonfluorescent Y chromosome.

Gänshirt-Ahlert D, Pawlowitzki IH, Gal A. Gänshirt-Ahlert D, et al. Among authors: gal a. Hum Genet. 1987 Jun;76(2):153-6. doi: 10.1007/BF00284913. Hum Genet. 1987. PMID: 2886420

7

[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.

8

Ring Y chromosome: molecular characterization by DNA probes.

Pohlschmidt M, Rappold G, Krause M, Ahlert D, Hosenfeld D, Weissenbach J, Gal A. Pohlschmidt M, et al. Among authors: gal a. Cytogenet Cell Genet. 1991;56(2):65-8. doi: 10.1159/000133051. Cytogenet Cell Genet. 1991. PMID: 2013232

9

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

10

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.

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