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(2020) Indirect Molecular Diagnosis of Congenital Factor XIII Deficiency by Candidate Microsatellites and Single Nucleotide Polymorphisms. Iranian Journal of Pediatric Hematology and Oncology. pp. 114-130. ISSN 2008-8892
(2020) Indirect molecular diagnosis of congenital factor ΧIII deficiency by candidate microsatellites and single nucleotide polymorphisms. Iranian Journal of Pediatric Hematology and Oncology. pp. 114-130. ISSN 20088892 (ISSN)
(2016) Spectrum of factor X gene mutations in Iranian patients with congenital factor X deficiency. Blood Coagulation & Fibrinolysis. pp. 324-327. ISSN 0957-5235
(2014) Congenital factor V deficiency, comparison the severity of clinical presentations among patients with rare bleeding disorders. Haemophilia. p. 107. ISSN 1351-8216
(2014) Long term two central follow up study on a large group of patients with congenital factor XIII deficiency treated prophylactically with Fibrogammin P (R). Haemophilia. p. 107. ISSN 1351-8216
(2014) Molecular analysis, clinical manifestations and management of factor XIII deficiency in Southeast of Iran. Haemophilia. p. 108. ISSN 1351-8216