Alpha-thalassaemia in association with beta-thalassaemia patients in Malaysia: A study on the co-inheritance of both disorders

Community Genetics

Volumn 11, Issue 3, 2008, Pages 129-134

  Wee, Y C ^a   Tan, K L ^a   Kuldip, K ^a   Tai, K S ^a   George, E ^c   Tan, P C ^a   Chia, P ^b   Subramaniam, R ^b   Yap, S F ^a   Tan, J A M A ^a  

^a UNIVERSITY OF MALAYA   (Malaysia)

^b Fetal Medicine and Gynaecology Centre   (Malaysia)

^c UNIVERSITY PUTRA MALAYSIA   (Malaysia)

Author keywords

Thalassaemia; Thalassaemia; Amplification refractory mutation system; Duplex PCR; Gap PCR; Hb Bart's hydrops foetalis; PCR RFLP; Southeast Asian deletion

Indexed keywords

BETA GLOBIN;

ALPHA THALASSEMIA; ARTICLE; BETA THALASSEMIA; DISEASE ASSOCIATION; FEMALE; FETUS HYDROPS; GENE DELETION; GENE FREQUENCY; GENE MUTATION; GENETIC RISK; HETEROZYGOSITY; HETEROZYGOTE; HUMAN; INCIDENCE; INHERITANCE; MAJOR CLINICAL STUDY; MALAYSIA; MALE; POPULATION GENETICS; PRIORITY JOURNAL; SOUTHEAST ASIA;

ALPHA-THALASSEMIA; ASIAN CONTINENTAL ANCESTRY GROUP; BETA-THALASSEMIA; CHINA; FEMALE; HETEROZYGOTE; HUMANS; INDIA; INHERITANCE PATTERNS; LINKAGE (GENETICS); MALAYSIA; MALE; PREGNANCY; PRENATAL DIAGNOSIS; RETROSPECTIVE STUDIES;

EID: 41549153894     PISSN: 14222795     EISSN: None     Source Type: Journal    
DOI: 10.1159/000113874     Document Type: Article

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