Types of α-Globin Gene Deficiencies in Chinese Newborn Babies in the Guangxi Region, P.R. China (English)
- New search for: Zhao, Jing-Bo
- New search for: Zhao, Lin
- New search for: Gu, Y-C.
- New search for: Huisman, T. H. J.
- New search for: Zhao, Jing-Bo
- New search for: Zhao, Lin
- New search for: Gu, Y-C.
- New search for: Huisman, T. H. J.
In:
Hemoglobin
;
16
, 4
;
325-328
;
1992
- Article (Journal) / Electronic Resource
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Title:Types of α-Globin Gene Deficiencies in Chinese Newborn Babies in the Guangxi Region, P.R. China
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Contributors:Zhao, Jing-Bo ( author ) / Zhao, Lin ( author ) / Gu, Y-C. ( author ) / Huisman, T. H. J. ( author )
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Published in:Hemoglobin ; 16, 4 ; 325-328
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Publisher:
- New search for: Taylor & Francis
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Publication date:1992-01-01
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Size:4 pages
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ISSN:
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DOI:
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Type of media:Article (Journal)
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Type of material:Electronic Resource
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Language:English
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Source:
Table of contents – Volume 16, Issue 4
The tables of contents are generated automatically and are based on the data records of the individual contributions available in the index of the TIB portal. The display of the Tables of Contents may therefore be incomplete.
- 237
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The β- and δ-Thalassemia RepositoryHuisman, T. H. J. et al. | 1992
- 259
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A new Variant, Hb Muscat [α2β232(B14)Leu→val] Observed in Association With Hb S in an Arabian FamilyRamachandran, M. / Gu, L-H. / Wilson, J. B. / Kitundu, M. N. / Adekile, A. D. / Liu, J-C. / McKie, K. M. / Huisman, T. H. J. et al. | 1992
- 267
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Hb Bab-Saaooun or α2β248(CD7)Leu→pro, A Mildly Unstable Variant Found in an Arabian Boy from TunisiaMolchanova, T. P. / Wilson, J. B. / Gu, L-H. / Guemira, F. / Fattoum, S. / Huisman, T. H. J. et al. | 1992
- 275
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Hb Prato α31(B12)Arg→ser] in a Calabrian FamilyDe Marco, E. V. / Crescibene, L. / Pasqua, A. / Brancati, C. / Bria, M. / Qualtieri, A. et al. | 1992
- 281
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Erythrocytosis Secondary to Hb Bunbury [α2β294(FG1)Asp→asn]Ballas, S. K. / Park, D. / Fernandez, L. / Hine, T. K. / Jue, D. L. / Johnson, M. H. / Moo-Penn, W. F. et al. | 1992
- 287
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Anomalous Results from a new Hematology Analyzer Reveal HemoglobinopathiesLaharrague, P. F. / Corberand, J. X. / Fillola, G. / Cambus, J. P. et al. | 1992
- 291
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A Mutation at CDS 82/83 (-G) Observed in a Yugoslavian Family with a Heterozygosity for β-ThalassemiaJankovic, L. / Dimovski, A. J. / Efremov, G. D. / Juricic, D. et al. | 1992
- 295
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Two β-Thalassemia Mutations in Japan: Codon 121 (Gaa→Taa) and IVS-I-130 (G→C)Yamamoto, Ku. / Yamamoto, Ki. / Hattori, Y. / Yamashiro, Y. / Hoshitani, M. / Morishita, M. / Ohba, Y. / Katahira, H. / Karasawa, M. / Omine, M. et al. | 1992
- 303
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Japanese β-Thalassemia [Codon 90 (GAG→TAG)] Has at Least two OriginsHattori, Y. / Yamashiro, Y. / Ohba, Y. / Miyaji, T. / Terai, S. / Morishita, M. / Yamamoto, Ku. / Yamamoto, Ki. / Matsumoto, N. / Kawano, F. et al. | 1992
- 309
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A Novel Frameshift Mutation: Deletion of C in Codons 74/75 of the β-Globin Gene Causes β°-Thalassemia in a Turkish PatientBaşak, A. N. / Özer, A. / Özçelik, H. / Kirdar, B. / Gürgey, A. et al. | 1992
- 313
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A β-Thalassemia Mutation Found in KoreaKoo, M. S. / Kim, S. I. / Cho, H. I. / Hattori, Y. / Yamashiro, Y. / Hoshitani, M. / Ohba, Y. / Miyaji, T. / Yamamoto, Ku. / Yamamoto, Ki. et al. | 1992
- 321
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Mild HB Constant Spring-HB H Disease with β°-Thalassemia TraitWen, X-J. / Liang, S. et al. | 1992
- 325
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Types of α-Globin Gene Deficiencies in Chinese Newborn Babies in the Guangxi Region, P.R. ChinaZhao, Jing-Bo / Zhao, Lin / Gu, Y-C. / Huisman, T. H. J. et al. | 1992
- 329
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Special FeatureHuisman, T. H. J. et al. | 1992
- 331
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Hemoglobinopathies in SardiniaMasala, Bruno et al. | 1992