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Carrier detection by DNA analysis in Duchenne muscular dystrophy families.
Turk J Pediatr. 1992 Apr-Jun;34(2):79-92.
Turk J Pediatr. 1992.
PMID: 1440954
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: kuseyri f.
Hum Genet. 1992 Aug;89(6):635-9. doi: 10.1007/BF00221954.
Hum Genet. 1992.
PMID: 1355068
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Neu-Laxova syndrome: report of a case from Turkey.
Kuseyri F, Bilge I, Bilgiç L, Apak MY.
Kuseyri F, et al.
Clin Genet. 1993 May;43(5):267-9. doi: 10.1111/j.1399-0004.1993.tb03815.x.
Clin Genet. 1993.
PMID: 8375108
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Screening of deletions and RFLP analysis in Turkish DMD/BMD families by PCR.
Gökgöz N, Kuseyri F, Topaloğlu H, Yüksel-Apak M, Kirdar B.
Gökgöz N, et al. Among authors: kuseyri f.
Clin Genet. 1993 May;43(5):261-6. doi: 10.1111/j.1399-0004.1993.tb03814.x.
Clin Genet. 1993.
PMID: 8104108
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Clinical, ultrastructural and biochemical studies in two sibs with Ehlers-Danlos syndrome type VI-B-like features.
Oğur G, Baykan N, De Paepe A, Steinmann B, Quatacker J, Kuseyrí F, Yüksel-Apak M.
Oğur G, et al. Among authors: kuseyri f.
Clin Genet. 1994 Dec;46(6):417-22. doi: 10.1111/j.1399-0004.1994.tb04409.x.
Clin Genet. 1994.
PMID: 7889658
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Tetra-amelia, lung hypo-/aplasia, cleft lip-palate, and heart defect: a new syndrome?
Başaran S, Yüksel A, Ermiş H, Kuseyri F, Ağan M, Yüksel-Apak M.
Başaran S, et al. Among authors: kuseyri f.
Am J Med Genet. 1994 May 15;51(1):77-80. doi: 10.1002/ajmg.1320510116.
Am J Med Genet. 1994.
PMID: 8030673
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