Frey D - Search Results

1

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: frey d. 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.

2

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: frey d. Hum Genet. 1986 Jul;73(3):271-5. doi: 10.1007/BF00401243. Hum Genet. 1986. PMID: 3015771

3

Gene deletion in a patient with chronic granulomatous disease and McLeod syndrome: fine mapping of the Xk gene locus.

Frey D, Mächler M, Seger R, Schmid W, Orkin SH. Frey D, et al. Blood. 1988 Jan;71(1):252-5. Blood. 1988. PMID: 3334897 Free article.

4

Analysis of the gene and gene product in patients with X linked chronic granulomatous disease (XL-CGD).

Frey D, Mühlebach T, Seger R. Frey D, et al. Acta Paediatr Hung. 1988-1989;29(1-2):185-9. Acta Paediatr Hung. 1988. PMID: 3255401 No abstract available.

5

Localization of the McLeod locus (XK) within Xp21 by deletion analysis.

Bertelson CJ, Pogo AO, Chaudhuri A, Marsh WL, Redman CM, Banerjee D, Symmans WA, Simon T, Frey D, Kunkel LM. Bertelson CJ, et al. Among authors: frey d. Am J Hum Genet. 1988 May;42(5):703-11. Am J Hum Genet. 1988. PMID: 3358422 Free PMC article.

6

Molecular deletion patterns in Duchenne and Becker type muscular dystrophy.

Liechti-Gallati S, Koenig M, Kunkel LM, Frey D, Boltshauser E, Schneider V, Braga S, Moser H. Liechti-Gallati S, et al. Among authors: frey d. Hum Genet. 1989 Mar;81(4):343-8. doi: 10.1007/BF00283688. Hum Genet. 1989. PMID: 2784778

7

Short stature: a common feature in Duchenne muscular dystrophy.

Eiholzer U, Boltshauser E, Frey D, Molinari L, Zachmann M. Eiholzer U, et al. Among authors: frey d. Eur J Pediatr. 1988 Aug;147(6):602-5. doi: 10.1007/BF00442472. Eur J Pediatr. 1988. PMID: 3181201

8

Relationship of Serum Bicarbonate Levels with 1-Year Graft Function in Kidney Transplant Recipients in Switzerland.

Wiegand A, Graf N, Bonani M, Frey D, Wüthrich RP, Mohebbi N. Wiegand A, et al. Among authors: frey d. Kidney Blood Press Res. 2019;44(5):1179-1188. doi: 10.1159/000502527. Epub 2019 Sep 19. Kidney Blood Press Res. 2019. PMID: 31536994 Free article.

9

Pure red cell aplasia of long duration complicating major ABO-incompatible bone marrow transplantation.

Gmür JP, Burger J, Schaffner A, Neftel K, Oelz O, Frey D, Metaxas M. Gmür JP, et al. Among authors: frey d. Blood. 1990 Jan 1;75(1):290-5. Blood. 1990. PMID: 2294993 Free article.

10

Down's syndrome with XYY additional aneuploidy.

Stoll C, Frey D, Willard D, Messer J. Stoll C, et al. Among authors: frey d. Hum Genet. 1976 Sep 10;34(1):85-8. doi: 10.1007/BF00284442. Hum Genet. 1976. PMID: 134970 No abstract available.

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