A report of 8 cases with hemoglobin H disease in an Iranian family.

Azarkeivan, Azita; Azita, Azarkeivan; Neishabury, Maryam; Hadavi, Valeh; Esteghamat, Fatemehsadat; Fatemehsadat, Esteghamat; Enrahimkhani, Saideh; Najmabadi, Hossein; Hossein, Najmabadi

Azarkeivan, Azita; Azita, Azarkeivan; Neishabury, Maryam; Hadavi, Valeh; Esteghamat, Fatemehsadat; Fatemehsadat, Esteghamat; Enrahimkhani, Saideh; Najmabadi, Hossein; Hossein, Najmabadi.

Affiliation

Azarkeivan A; Research Center of Iranian Blood Transfusion Organization, Thalassemia Clinic, Tehran, Iran. azazarkeivan@yahoo.com

Pediatr Hematol Oncol ; 27(5): 405-12, 2010 Aug.

Article in En | MEDLINE | ID: mdl-20670167

Subject(s)

Hemoglobin H/genetics; alpha-Thalassemia/diagnosis; DNA Mutational Analysis; Family; Female; Genetic Testing; Genotype; Humans; Hydrops Fetalis/diagnosis; Iran; Middle Aged; Phenotype; Pregnancy; Prenatal Diagnosis; alpha-Thalassemia/genetics

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Hemoglobin H / Alpha-Thalassemia Type of study: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Limits: Female / Humans / Middle aged / Pregnancy Country/Region as subject: Asia Language: En Journal: Pediatr Hematol Oncol Journal subject: HEMATOLOGIA / NEOPLASIAS / PEDIATRIA Year: 2010 Document type: Article Affiliation country: Iran Country of publication: United kingdom

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