Ozalp I - 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: ozalp i. 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

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

3

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

4

Identification of mutations in the galactose-1-phosphate uridyltransferase (GALT) gene in 16 Turkish patients with galactosemia, including a novel mutation of F294Y. Mutation in brief no. 235. Online.

Seyrantepe V, Ozguc M, Coskun T, Ozalp I, Reichardt JK. Seyrantepe V, et al. Among authors: ozalp i. Hum Mutat. 1999;13(4):339. doi: 10.1002/(SICI)1098-1004(1999)13:4<339::AID-HUMU18>3.0.CO;2-S. Hum Mutat. 1999. PMID: 10220154

5

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: ozalp i. Turk J Pediatr. 1991 Apr-Jun;33(2):79-84. Turk J Pediatr. 1991. PMID: 1844185

6

Mutational analysis of Turkish galactosaemia patients.

Coskun T, Erkul E, Seyrantepe V, Ozgüç M, Tokatli A, Ozalp I. Coskun T, et al. Among authors: ozalp i. J Inherit Metab Dis. 1995;18(3):368-9. doi: 10.1007/BF00710438. J Inherit Metab Dis. 1995. PMID: 7474913 Clinical Trial. No abstract available.

7

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

8

Genetic and neurological evaluation of untreated and late-treated patients with phenylketonuria.

Ozalp I, Coşkun T, Ozgüç M, Tokatli A, Yalaz K, Vanli L, Yilmaz E, Erbay A. Ozalp I, et al. J Inherit Metab Dis. 1994;17(3):371. doi: 10.1007/BF00711834. J Inherit Metab Dis. 1994. PMID: 7807957 No abstract available.

9

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

10

Classical phenylketonuria associated with Goldenhar's syndrome. A case report.

Tokatli A, Coşkun T, Kocabaş CN, Ozalp I, Balci S. Tokatli A, et al. Among authors: ozalp i. Turk J Pediatr. 1994 Apr-Jun;36(2):153-6. Turk J Pediatr. 1994. PMID: 8016917

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