Erdem H - Search Results

1

Mutation analysis in Turkish phenylketonuria patients.

Ozgüç M, Ozalp I, Coşkun T, Yilmaz E, Erdem H, Ayter S. Ozgüç M, et al. Among authors: erdem h. J Med Genet. 1993 Feb;30(2):129-30. doi: 10.1136/jmg.30.2.129. J Med Genet. 1993. PMID: 8445616 Free PMC article.

2

Study of 12 mutations in Turkish cystic fibrosis patients.

Yilmaz E, Erdem H, Ozgüç M, Coşkun T, Ozçelik U, Göçmen A, Ozalp I. Yilmaz E, et al. Among authors: erdem h. Hum Hered. 1995 May-Jun;45(3):175-7. doi: 10.1159/000154281. Hum Hered. 1995. PMID: 7542223

3

Association between mutations and the variable number tandem repeat alleles in a sample of Turkish phenylketonuria patients.

Ozgüç M, Yilmaz E, Erdem H, Coşkun T, Tokatli A, Ozalp I. Ozgüç M, et al. Among authors: erdem h. J Inherit Metab Dis. 1994;17(3):373-4. doi: 10.1007/BF00711836. J Inherit Metab Dis. 1994. PMID: 7807959 No abstract available.

4

Frequency of the IVS-10nt546 mutation in 44 Turkish phenylketonuria patients.

Ozgüç M, Ozalp I, Coşkun T, Yilmaz E, Erdem H, Ayter S. Ozgüç M, et al. Among authors: erdem h. Turk J Pediatr. 1993 Jan-Mar;35(1):11-4. Turk J Pediatr. 1993. PMID: 7901929

5

Allele frequencies of Mp6D-9 and GATT markers in 32 Turkish cystic fibrosis families.

Ozgüç M, Yilmaz E, Erdem H, Coşkun T, Ozçelik U, Togan I, Göçmen A, Ayter S, Ozalp I. Ozgüç M, et al. Among authors: erdem h. Clin Genet. 1994 May;45(5):266-8. doi: 10.1111/j.1399-0004.1994.tb04153.x. Clin Genet. 1994. PMID: 8076413

6

Mutations of the CFTR gene in Turkish patients with congenital bilateral absence of the vas deferens.

Dayangaç D, Erdem H, Yilmaz E, Sahin A, Sohn C, Ozgüç M, Dörk T. Dayangaç D, et al. Among authors: erdem h. Hum Reprod. 2004 May;19(5):1094-100. doi: 10.1093/humrep/deh223. Epub 2004 Apr 7. Hum Reprod. 2004. PMID: 15070876

7

Analysis of delta F508 mutation in cystic fibrosis pathology specimens.

Ozgüç M, Tekin A, Erdem H, Yilmaz E, Ayter S, Coşkun T, Can A, Gögüş S, Caglar M, Kale G, et al. Ozgüç M, et al. Among authors: erdem h. Pediatr Pathol. 1994 May-Jun;14(3):491-6. doi: 10.3109/15513819409024278. Pediatr Pathol. 1994. PMID: 7520582

8

Deletion analysis of Duchenne muscular dystrophy.

Erdem H, Ayter S, Ozgüç M, Topçu M, Topaloğlu H, Renda Y. Erdem H, et al. Turk J Pediatr. 1993 Jan-Mar;35(1):15-21. Turk J Pediatr. 1993. PMID: 8236513

9

Allele distribution of D5S125, MAP1B5' and D5S679 microsatellite markers in Turkish spinal muscular atrophy families.

Erdem H, Pehlivan S, Topaloğlu H, Togan I, Ozgüç M. Erdem H, et al. Turk J Pediatr. 1997 Oct-Dec;39(4):447-52. Turk J Pediatr. 1997. PMID: 9433145

10

Deletion analysis in Turkish patients with spinal muscular atrophy.

Erdem H, Pehlivan S, Topaloglu H, Ozgüç M. Erdem H, et al. Brain Dev. 1999 Mar;21(2):86-9. doi: 10.1016/s0387-7604(98)00063-1. Brain Dev. 1999. PMID: 10206524

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