Telatar M - Search Results

1

Carrier detection by DNA analysis in Duchenne muscular dystrophy families.

Battaloğlu E, Telatar M, Deymeer F, Serdaroğlu P, Ozdemir C, Kuseyri F, Apak MY, Tolun A. Battaloğlu E, et al. Among authors: telatar m. Turk J Pediatr. 1992 Apr-Jun;34(2):79-92. Turk J Pediatr. 1992. PMID: 1440954

2

DNA analysis in Turkish Duchenne/Becker muscular dystrophy families.

Battaloğlu E, Telatar M, Deymeer F, Serdaroğlu P, Kuseyri F, Ozdemir C, Apak M, Tolun A. Battaloğlu E, et al. Among authors: telatar m. Hum Genet. 1992 Aug;89(6):635-9. doi: 10.1007/BF00221954. Hum Genet. 1992. PMID: 1355068

3

Identification of a one-basepair deletion in exon 6 of the dystrophin gene.

Kavaslar GN, Telatar M, Serdaroglu P, Deymeer F, Ozdemir C, Tolun A. Kavaslar GN, et al. Among authors: telatar m. Hum Mutat. 1995;6(1):85-6. doi: 10.1002/humu.1380060116. Hum Mutat. 1995. PMID: 7550238 No abstract available.

4

Dinucleotide repeat polymorphism at 11q23.

Telatar M, Concannon P, Tolun A. Telatar M, et al. Hum Genet. 1994 Jul;94(1):109. doi: 10.1007/BF02272856. Hum Genet. 1994. PMID: 8034289

5

Dinucleotide repeat polymorphism at the NCAM locus.

Telatar M, Concannon P, Tolun A. Telatar M, et al. Hum Mol Genet. 1994 May;3(5):842. doi: 10.1093/hmg/3.5.842. Hum Mol Genet. 1994. PMID: 8081382 No abstract available.

6

Ataxia-telangiectasia: linkage analysis of chromosome 11q22-23 markers in Turkish families.

Sanal O, Lange E, Telatar M, Sobel E, Salazar-Novak J, Ersoy F, Morrison A, Concannon P, Tolun A, Gatti RA. Sanal O, et al. Among authors: telatar m. FASEB J. 1992 Jul;6(10):2848-52. doi: 10.1096/fasebj.6.10.1634048. FASEB J. 1992. PMID: 1634048

7

Cystic fibrosis patients from the Black Sea region: the 1677delTA mutation.

Angelicheva D, Boteva K, Jordanova A, Savov A, Kufardjieva A, Tolun A, Telatar M, Akarsubaşi A, Köprübaşi F, Aydoğdu S, et al. Angelicheva D, et al. Among authors: telatar m. Hum Mutat. 1994;3(4):353-7. doi: 10.1002/humu.1380030405. Hum Mutat. 1994. PMID: 8081388

8

Splicing defects in the ataxia-telangiectasia gene, ATM: underlying mutations and consequences.

Teraoka SN, Telatar M, Becker-Catania S, Liang T, Onengüt S, Tolun A, Chessa L, Sanal O, Bernatowska E, Gatti RA, Concannon P. Teraoka SN, et al. Among authors: telatar m. Am J Hum Genet. 1999 Jun;64(6):1617-31. doi: 10.1086/302418. Am J Hum Genet. 1999. PMID: 10330348 Free PMC article.

9

New localization of NCAM, proximal to DRD2 at chromosome 11q23.

Telatar M, Lange E, Uhrhammer N, Gatti RA. Telatar M, et al. Mamm Genome. 1995 Jan;6(1):59-60. doi: 10.1007/BF00350901. Mamm Genome. 1995. PMID: 7719033 No abstract available.

10

CAND3: a ubiquitously expressed gene immediately adjacent and in opposite transcriptional orientation to the ATM gene at 11q23.1.

Chen X, Yang L, Udar N, Liang T, Uhrhammer N, Xu S, Bay JO, Wang Z, Dandakar S, Chiplunkar S, Klisak I, Telatar M, Yang H, Concannon P, Gatti RA. Chen X, et al. Among authors: telatar m. Mamm Genome. 1997 Feb;8(2):129-33. Mamm Genome. 1997. PMID: 9060412

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