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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 4, 2023. (Total: 217641Documents)
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Records 1 - 4 (of 4 Records)

Query Trace: Abnormalities and HBB[original query]
Genetic basis of persistent red blood cell microcytosis in the Chinese unexplained by phenotypical testing.
Journal of clinical pathology 2015 Jan 68 (1): 69-72.
So Chi-Chiu, Liu Ada K, Tsang Mandy H, Ngai Donna Y, Leung Kin-Sang, Chan Amy
Newborn Screening for Hemoglobinopathies and Red Cell Enzymopathies in Tripura State: A Malaria-Endemic State in Northeast India.
Hemoglobin 2018 2 42 (1): 43-46.
Upadhye Dipti, Das Rajat S, Ray Jayanta, Acharjee Shukdeb, Ghosh Kanjaksha, Colah Roshan B, Mukherjee Malay
Hb S (HBB: c.20A>T) and ?- and ?-Thalassemia Coinheritance in Iranian Patients.
Hemoglobin 2020 5 44 (2): 109-112.
Azarkeivan Azita, Cohan Nader, Niazkar Hamid Reza, Azizi Arsalan, Rad Fari
Clinical Severity of ?-Thalassemia Pediatric Patients in Myanmar.
Hemoglobin 2022 8 46 (1): 66-70.
Khaing Aye Aye, Myint Phyu Phyu, Paiboonsukwong Kittiphong, Win Ne, Fucharoen Suthat, Sripichai Orap
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