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Journal of Inherited Metabolic Disease|July 18, 2002
Maple syrup urine disease: mutation analysis in Turkish patientsA Dursun, M Henneke, K Ozgül, et al.Human Genetics|January 12, 2001
Molecular analysis of 16 Turkish families with DHPR deficiency using denaturing gradient gel electrophoresis (DGGE)A Romstad, H S Kalkanoğlu, T Coşkun, et al.JIMD Reports|February 23, 2013
Identification of mutations and evaluation of cardiomyopathy in Turkish patients with primary carnitine deficiencyM Kilic, R K Ozgül, T Coşkun, et al.International Journal of Pediatric Otorhinolaryngology|December 13, 2006
Audiologic findings in children with biotinidase deficiency in TurkeyG A Genc, H S Sivri-Kalkanoğlu, A Dursun, et al.Nucleosides, Nucleotides & Nucleic Acids|October 27, 2006
A Turkish case with molybdenum cofactor deficiencyK Ichida, H Ibrahim Aydin, M Hosoyamada, et al.The Journal of Pediatrics|March 20, 1998
Delayed-onset profound biotinidase deficiencyB Wolf, R J Pomponio, K J Norrgard, et al.Human Heredity|May 9, 2000
Fine mapping of the human biotinidase gene and haplotype analysis of five common mutationsS H Blanton, A Pandya, B L Landa, et al.Pageof 3