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Search Results - Ngouprommin, L.~
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Genetic compound heterozygosity for Southeast Asian ovalocytosis and thalassemia in Thailand: prevalence and phenotypic analysis
by
Ngouprommin, L.
,
Sae-ung, N.
,
Fucharoen, S.
,
Fucharoen, G.
,
Sanchaisuriya, K.
,
Jetsrisuparb, A.
Published in
Clinical genetics
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Etiology and outcome of non-immune hydrops fetalis in relation to gestational age at diagnosis and intrauterine treatment
by
Chainarong, Natthicha
,
Muangpaisarn, Worachot
,
Suwanrath, Chitkasaem
Published in
Journal of perinatology
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Trans-acting genetic modifiers of clinical severity in heterozygous β-Thalassemia trait
by
Loh, Joanna B.
,
Ross, Jules M.
,
Musallam, Khaled M.
,
Kuo, Kevin H. M.
Published in
Annals of hematology
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Concurrent β-thalassaemia trait and Southeast Asian ovalocytosis associated with clinically significant iron loading
by
Chen, Yunxin
,
Law, Hai Yang
,
Tan, Guek Peng
,
Ang, Ai Leen
Published in
Blood cells, molecules, & diseases
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The evolutionary origins of Southeast Asian Ovalocytosis
by
Paquette, A.M.
,
Harahap, A.
,
Laosombat, V.
,
Patnode, J.M.
,
Satyagraha, A.
,
Sudoyo, H.
,
Thompson, M.K.
,
Yusoff, N.M.
,
Wilder, J.A.
Published in
Infection, genetics and evolution
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Annals Of Hematology
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Anion Exchange Protein 1, Erythrocyte - Genetics
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Elliptocytosis, Hereditary - Genetics
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Gene Frequency
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Hematology
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Heterozygote
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692/700/139/1735
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692/700/1421
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