Výsledky vyhledávání - "Noor-Adilah Jaapar"

A Case Series of α-Thalassemia Intermedia Due to Compound Heterozygosity for Hb Adana [HBA2: c179G>A (orHBA1); p.Gly60Asp] With Other α-Thalassemias in Malay Families

Autor: Ainoon Othman, Hafiza Alauddin, Azma Rz, Noor-Farisah Razak, Noor-Adilah Jaapar, Zarina Abdul-Latiff, Azlin Ithnin, Hamidah Alias, C-Khai Loh

Publikováno v: Hemoglobin. 38:277-281

Hb Adana [HBA2: c179G>A (or HBA1); p.Gly60Asp] is a rare hemoglobin (Hb) variant due to a mutation at codon 59 of the α2- or α1-globin gene resulting in a glycine to aspartic acid substitution. Two siblings with a unique coinheritance of Hb Adana a

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1098d29d3d51d26562d1b7b77897bbdc
https://doi.org/10.3109/03630269.2014.916720

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A rare t (9; 12; 22) (q34; q23; q11) translocation in a patient with typical chronic myeloid leukemia: A case report

Autor: Noor Adilah Jaapar, Noor Hamidah Hussin, Zubaidah Zakaria, Chia Wai Kit, Suria Abdul Aziz, Sharifah Noor Akmal, Hafiza Alauddin, Salwati Shuib, Azlin Ithnin, Rafeah Tumian, Azma Rz

Publikováno v: Journal of Hematological Malignancies. 2

Chronic myeloid leukaemia (CML) is typically associated with reciprocal translocation between long arms of chromosome 9 and 22, t (9, 22) (q34; q11.2) and with the formation of a BCR-ABL fusion gene. In a minority of newly diagnosed CML cases, comple

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::e6c73d6df494aaacf821c86f9bc69c9d
https://doi.org/10.5430/jhm.v2n4p17

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