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Humangenetik|November 6, 1975
Human triploid cell strain. Phenotype on cellular levelA M Kuliev, V I Kukharenko, K N Grinberg, et al.Human Genetics|September 22, 1977
Monosomy 21 in a human spontaneous abortus. Morphogenetic disturbances and phenotype at the cellular levelA M Kuliev, K N Grinberg, V I Kukharenko, et al.Vestnik Khirurgii Imeni I. I. Grekova|August 1, 1988
[Arthroplasty of the hip joint in children and adolescents with congenital hip dislocation]V L Andrianov, A M Kuliev, E S Tikhonenkov, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 1, 1985
Diagnostic fetal blood sampling for the haemoglobinopathies--10-year experienceS Kanokpongsukdi, R H Ward, M Petrou, et al.Annals of the New York Academy of Sciences|December 13, 2005
Quality of life in thalassemiaP Telfer, G Constantinidou, P Andreou, et al.Archives of Disease in Childhood|May 1, 1995
Psychosocial and clinical burden of thalassaemia intermedia and its implications for prenatal diagnosisS Ratip, D Skuse, J Porter, et al.Clinical and Experimental Immunology|August 1, 1987
Human fetal lymphocytes require T cell growth factors for cytotoxic responsesL S Rayfield, L Brent, A Boylston, et al.Journal of Community Genetics|April 24, 2023
A review of key terminology and definitions used for birth defects globallyH L Malherbe, B Modell, H Blencowe, et al.Lancet (London, England)|September 13, 1980
Thalassaemia as a model of recessive genetic disease in the communityM Mouzouras, L Camba, P Ioannou, et al.Clinical and Laboratory Haematology|February 15, 2000
Lifetime treatment costs of beta-thalassaemia majorJ Karnon, D Zeuner, J Brown, et al.Pageof 10