Alpha- and beta-thalassemia in Thailand
ชื่อเรื่อง
Alpha- and beta-thalassemia in Thailand
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ผู้สร้าง/เจ้าของผลงาน
Wasi, Prawase
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Na-Nakorn, Supa
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Pootrakul, Sa-nga
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Sookanek, Munsit
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Disthasongchan, Pensri
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Pornpatkul, Malida
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Panich, Vicharn
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หัวเรื่อง
History and Philosophy of Science
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General Biochemistry, Genetics and Molecular Biology
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General Neuroscience
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คำอธิบายรายละเอียดของเอกสาร
This study was supported by United States Public Health Service Grant AM 09805 from the National Institute of Arthritis and Metabolic Diseases.
บทคัดย่อ
In Thailand, both a- and ß-thalassemia are widespread and there is more than one subtype in each variety. Hemoglobin (Hb) E which is is a2, p;6G'u+L (Hunt & Ingram, 1959) is remarkably frequent (Na-Nakorn et al., 1956; Sundharagiati et al. 1958, 1959a, 1959b; Flatz et al., 1965; Wasi et al., 1967a), reaching 50 percent in certain areas. These abnormal genes in different combinations result in a spectrum of syndromes ranging from asymptomatic heterozygotes to lethal Hb Bart's hydrops fetalis. Attempts have been made to characterize the various genotypes by clinical, hematologic, biochemical, genetic and cord blood studies. This paper summarizes the manifestations of these syndromes, with particular emphasis on the
diseased forms
diseased forms
ผู้ร่วมงาน
Division of Hematology. Department of Medicine Siriraj Hospital Medical School. Bangkok, Thailand
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ปีที่ผลิตเอกสาร
วันที่บันทึกข้อมูล
2023-04-28
ประเภท
Article
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รูปแบบ
ขนาดหรือจำนวนของเอกสาร
23 pages
ต้นฉบับ/แหล่งที่มาของเอกสาร
Annals of the New York Academy of Sciences, Vol. 165, Page 60-82
ภาษา
รหัส หรือตัวบ่งชี้เอกสาร
ขอบเขต
เจ้าของลิขสิทธิ์
John Wiley & Sons, Inc.
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