3 results for author:"Yalnizoglu D." in Literature citations
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| Identification of a novel Twinkle mutation in a family with infantile onset spinocerebellar ataxia by whole exome sequencing. Dundar H., Ozgul R.K., Yalnizoglu D., Erdem S., Oguz K.K., Tuncel D., Temucin C.M., Dursun A. Pediatr. Neurol. 46:172-177(2012) · UniProtKB (1) · Mapped (3) |
| Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Bilguvar K., Ozturk A.K., Louvi A., Kwan K.Y., Choi M., Tatli B., Yalnizoglu D., Tuysuz B., Caglayan A.O., Gokben S. et al. |
| A biochemical, genetic, and clinical survey of autosomal recessive limb girdle muscular dystrophies in Turkey. Dincer P., Leturcq F., Richard I., Piccolo F., Yalnizoglu D., de Toma C., Akcoeren Z., Broux O., Deburgrave N., Brenguier L. et al. Ann. Neurol. 42:222-229(1997) · UniProtKB (1) |