Samanns C - Search Results

1

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: samanns c. Hum Genet. 1991 Dec;88(2):162-6. doi: 10.1007/BF00206065. Hum Genet. 1991. PMID: 1684563

2

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: samanns c. Clin Genet. 1992 Mar;41(3):135-8. doi: 10.1111/j.1399-0004.1992.tb03649.x. Clin Genet. 1992. PMID: 1348665

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: samanns c. Ophthalmic Paediatr Genet. 1990 Sep;11(3):165-70. doi: 10.3109/13816819009020975. Ophthalmic Paediatr Genet. 1990. PMID: 2280973

4

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: samanns c. Hum Genet. 1991 Jan;86(3):265-7. doi: 10.1007/BF00202406. Hum Genet. 1991. PMID: 1997379

5

Gene for non-specific X-linked mental retardation maps in the pericentromeric region.

Samanns C, Albrecht R, Neugebauer M, Neri G, Gal A. Samanns C, et al. Am J Med Genet. 1991 Feb-Mar;38(2-3):224-7. doi: 10.1002/ajmg.1320380210. Am J Med Genet. 1991. PMID: 2018062

6

Gene of type II autosomal dominant retinitis pigmentosa maps on the long arm of chromosome 3.

Olsson JE, Samanns C, Jimenez J, Pongratz J, Chand A, Watty A, Seuchter SA, Denton M, Gal A. Olsson JE, et al. Among authors: samanns c. Am J Med Genet. 1990 Apr;35(4):595-9. doi: 10.1002/ajmg.1320350434. Am J Med Genet. 1990. PMID: 2333895

7

[Autosomal dominant hereditary retinopathia pigmentosa with genetic heterogeneity].

Orth U, Samanns C, Gusseck H, Niemeyer G, Ludwig M, Meitinger T, Schinzel A, Schwinger E, Gal A. Orth U, et al. Among authors: samanns c. Fortschr Ophthalmol. 1991;88(5):455-9. Fortschr Ophthalmol. 1991. PMID: 1757031 German.

8

Molecular analysis and genetic mapping of the rhodopsin gene in families with autosomal dominant retinitis pigmentosa.

Bunge S, Wedemann H, David D, Terwilliger DJ, van den Born LI, Aulehla-Scholz C, Samanns C, Horn M, Ott J, Schwinger E, et al. Bunge S, et al. Among authors: samanns c. Genomics. 1993 Jul;17(1):230-3. doi: 10.1006/geno.1993.1309. Genomics. 1993. PMID: 8406457

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