Zobrazeno 1 - 6 of 6 pro vyhledávání: '"J G, Hendy"'
3
Hb Khartoum [beta124(H2)Pro--Arg] in a Vietnamese female
Autor: K. Garofalo, J. G. Hendy, D. K. Bowden
Publikováno v: Hemoglobin. 23(3)
Hb Khartoum [β124(H2)Pro→Arg] was first identified during screening for hemoglobinopathies in Khartoum (1). The abnormal hemoglobin (Hb), which comprised approximately 30% of the total Hb, had an electrophoretic mobility similar to Hb S. Although
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bae5368e01e8033ba4209584b8bca276
https://pubmed.ncbi.nlm.nih.gov/10490144
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5
Hb Footscray or alpha 133(H16) Ser--Arg: a new hemoglobin variant
Autor: M. C. Owen, J. G. Hendy
Publikováno v: Hemoglobin. 18(1)
Hb Footscray, alpha 133(H16) Ser--Arg, is a newly described hemoglobin variant found in an adult male of Polish-Hungarian descent. Hematological data and stability by the isopropanol stability test were normal. The abnormal hemoglobin comprised 15% o
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::332dd1c2f50e1b1ed4b5379b7125a8dc
https://pubmed.ncbi.nlm.nih.gov/8195006
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6
Direct detection of beta thalassemic mutations: use of biotin-labelled allele specific probes
Autor: J. G. Hendy, M. N. Cauchi
Publikováno v: American journal of hematology. 34(2)
Mutations at positions beta IVS1-6, beta IVS1-110, and beta 39 of the beta globin gene are responsible for the three most common thalassemic genes in the Mediterranean population. The polymerase chain reaction (PCR) was employed to amplify a 536 base
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab80c7bccef4bf8704024eed2aa4b9f2
https://pubmed.ncbi.nlm.nih.gov/2339680
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Plný text Recenzováno Digitální knihovna AV ČR
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