Ozgüç M - Search Results

1

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. Turk J Pediatr. 1993 Jan-Mar;35(1):11-4. Turk J Pediatr. 1993. PMID: 7901929

2

Prenatal diagnosis of cystic fibrosis in a Turkish family.

Yilmaz E, Ozgüç M, Coşkun T, Beksaç S, Cakar N, Ayter S, Ozalp I. Yilmaz E, et al. Among authors: ozguc m. Turk J Pediatr. 1991 Apr-Jun;33(2):79-84. Turk J Pediatr. 1991. PMID: 1844185

3

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: ozguc m. Hum Hered. 1995 May-Jun;45(3):175-7. doi: 10.1159/000154281. Hum Hered. 1995. PMID: 7542223

4

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. J Inherit Metab Dis. 1994;17(3):373-4. doi: 10.1007/BF00711836. J Inherit Metab Dis. 1994. PMID: 7807959 No abstract available.

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. Clin Genet. 1994 May;45(5):266-8. doi: 10.1111/j.1399-0004.1994.tb04153.x. Clin Genet. 1994. PMID: 8076413

6

Deletion analysis of Duchenne muscular dystrophy.

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

7

Mutation analysis in Turkish phenylketonuria patients.

Ozgüç M, Ozalp I, Coşkun T, Yilmaz E, Erdem H, Ayter S. Ozgüç M, et al. 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.

8

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. Among authors: ozguc m. Turk J Pediatr. 1997 Oct-Dec;39(4):447-52. Turk J Pediatr. 1997. PMID: 9433145

9

Newborn PKU screening in Turkey: at present and organization for future.

Ozalp I, Coşkun T, Tokatli A, Kalkanoğlu HS, Dursun A, Tokol S, Köksal G, Ozgüc M, Köse R. Ozalp I, et al. Among authors: ozguc m. Turk J Pediatr. 2001 Apr-Jun;43(2):97-101. Turk J Pediatr. 2001. PMID: 11432505

10

Analysis of the modifying effects of TAP 1/2 genes on cystic fibrosis phenotype.

Ozbaş-Gerçeker F, Ozçelik U, Kiper N, Anadol D, Ayhan G, Yilmaz E, Erdem-Yurter H, Ozgüç M. Ozbaş-Gerçeker F, et al. Among authors: ozguc m. Turk J Pediatr. 2002 Apr-Jun;44(2):91-7. Turk J Pediatr. 2002. PMID: 12026214

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