Genetic disorders in haematological practice in India

Community Genetics

Volumn 5, Issue 3, 2002, Pages 197-200

  Mohanty, D ^a,b   Colah, R B ^a   Gorakshakar, A C ^a   Nadkarni, A H ^a   Phanasgaonkar, S P ^a   Shetty, S ^a   Ghosh, K ^a   Mukherjee, M B ^a  

^a NATIONAL INSTITUTE OF IMMUNOHAEMATOLOGY   (India)

^b KEM HOSPITAL   (India)

Author keywords

Community genetics; Haemophilia; India; Sickle cell disease; Thalassaemia

Indexed keywords

BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 9; HEMOGLOBIN E; HEMOGLOBIN S;

ALPHA THALASSEMIA; ARTICLE; BETA THALASSEMIA; CHORION VILLUS SAMPLING; DOT HYBRIDIZATION; FIRST TRIMESTER PREGNANCY; GENE DELETION; GENE MUTATION; GENETIC COUNSELING; GENETIC DISORDER; GENETIC POLYMORPHISM; GENOTYPE; HEALTH EDUCATION; HEMOGLOBINOPATHY; HEMOPHILIA; HETEROZYGOTE DETECTION; HUMAN; INDIA; INTRON; PRENATAL DIAGNOSIS; PREVALENCE; PRIORITY JOURNAL; SCREENING;

EID: 0036434178     PISSN: 14222795     EISSN: None     Source Type: Journal    
DOI: 10.1159/000066336     Document Type: Article

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