Zobrazeno 1 - 10
of 78
pro vyhledávání: '"Luan Eng Lie-Injo"'
Publikováno v:
Human Heredity; 1971, Vol. 21 Issue 4, p376-383, 8p
Autor:
Lopez, C.G., Luan Eng, Lie-Injo
Publikováno v:
Human Heredity; 1971, Vol. 21 Issue 2, p185-191, 7p
Autor:
Luan Eng, Lie-Injo, Pillay, R.P.
Publikováno v:
Acta Haematologica; 1964, Vol. 31 Issue 5, p282-288, 7p
Autor:
J. Ganesan, Luan Eng Lie-Injo
Publikováno v:
Acta Haematologica. 59:341-347
The haematological findings resulting from the interaction of Hb A2Indonesia trait with β-thalassaemia trait and HbA2Indtrait with Hb E trait are discussed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7850b4a6ae3e8d7f52414282b68cca6
https://doi.org/10.1159/000207785
https://doi.org/10.1159/000207785
Publikováno v:
Human Genetics. 53:87-90
Human alcohol dehydrogenase ADH2 and ADH3 were investigated in liver and stomach specimens of Chinese and Indians from West Malaysia. Eight-nine percent of the Chinese carry the atypical ADH2 type, a proportion very similar to that reported in Japane
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d98a2c05cb9aaee785560d7eeb11d3e
https://doi.org/10.1007/bf00289455
https://doi.org/10.1007/bf00289455
Publikováno v:
Blood. 54:1407-1416
Two Chinese patients with HbQ-alpha 2 74 Asp replaced by His beta 2- alpha-thalassemia, one HbQ-alpha 2 74 or 75 Asp replaced by His beta 2 carrier, and one HbG-alpha 2 30 Glu replaced by Gln beta 2 carrier were studied to determine the number of alp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d07f554a3e42f0042607fd5449eabc6
https://doi.org/10.1182/blood.v54.6.1407.1407
https://doi.org/10.1182/blood.v54.6.1407.1407
Publikováno v:
American Journal of Hematology. 6:17-25
The ratio of Ggamma to Agamma was studied in 13 normal healthy newborns and in eight neonates with hydrops fetalis due to homozygous alpha-thalassemia. The findings in the normal healthy newborns agreed with those of earlier reports. In homozygous al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7493c4563faf16121781af8a6d328fcc
https://doi.org/10.1002/ajh.2830060104
https://doi.org/10.1002/ajh.2830060104
Publikováno v:
Blood. 43:251-259
A 12-yr-old Malay boy who was studied because his youngest brother and both his parents had the slow-moving Hb X components (earlier reported to lead to Hb H disease when combined with α-thalassemia) was found to be homozygous for the same slow-movi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a4a611e5b898b28fca52dbfb7098ed2
https://doi.org/10.1182/blood.v43.2.251.251
https://doi.org/10.1182/blood.v43.2.251.251
Publikováno v:
American Journal of Hematology. 29:22-26
A Batak Indonesian from North Sumatra with hemoglobin (Hb) D Punjab (alpha 2 beta 2 121----Gln) and hemoglobin Constant Spring (Hb CoSp) is described. The 24-year-old man did not have clinical symptoms, and his hematological indices were normal. Howe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::419809f131847b238f25346c33baa333
https://doi.org/10.1002/ajh.2830290106
https://doi.org/10.1002/ajh.2830290106
Autor:
Luan Eng Lie-Injo
Publikováno v:
Clinica Chimica Acta. 72:83-87
The unusual behaviour of an α 1 -antitrypsin, probably genetically determined, found in the serum of a Filipino in San Francisco is described. On starch gel electrophoresis the α 1 -antitrypsin did not show any pattern or a very weak Pi MM type pat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5a414c1a33940419a92aeb6b9b7f9aa3
https://doi.org/10.1016/0009-8981(76)90038-3
https://doi.org/10.1016/0009-8981(76)90038-3