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- Scopus: eid_2-s2.0-0035018158
- PMID: 11325652
- WOS: WOS:000168303800018
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Article: Diagnosis of concurrent hemoglobin H disease and heterozygous β-thalassemia [1]
Title | Diagnosis of concurrent hemoglobin H disease and heterozygous β-thalassemia [1] |
---|---|
Authors | |
Keywords | Diagnosis Globin gene mutation Hb H disease β-thalassemia |
Issue Date | 2001 |
Citation | Haematologica, 2001, v. 86 n. 4, p. 432-433 How to Cite? |
Persistent Identifier | http://hdl.handle.net/10722/148230 |
ISSN | 2023 Impact Factor: 8.2 2023 SCImago Journal Rankings: 2.490 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kwan Ma, ES | en_US |
dc.contributor.author | Yin Chan, AY | en_US |
dc.contributor.author | Au, WY | en_US |
dc.contributor.author | Yeung, YM | en_US |
dc.contributor.author | Chan, LC | en_US |
dc.date.accessioned | 2012-05-29T06:11:39Z | - |
dc.date.available | 2012-05-29T06:11:39Z | - |
dc.date.issued | 2001 | en_US |
dc.identifier.citation | Haematologica, 2001, v. 86 n. 4, p. 432-433 | en_US |
dc.identifier.issn | 0390-6078 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/148230 | - |
dc.language | eng | en_US |
dc.relation.ispartof | Haematologica | en_US |
dc.subject | Diagnosis | - |
dc.subject | Globin gene mutation | - |
dc.subject | Hb H disease | - |
dc.subject | β-thalassemia | - |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Anemia, Hypochromic - Etiology | en_US |
dc.subject.mesh | Dna Mutational Analysis | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Globins - Genetics | en_US |
dc.subject.mesh | Heterozygote | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Mutation | en_US |
dc.subject.mesh | Pregnancy | en_US |
dc.subject.mesh | Pregnancy Complications, Hematologic | en_US |
dc.subject.mesh | Alpha-Thalassemia - Complications - Diagnosis - Genetics | en_US |
dc.subject.mesh | Beta-Thalassemia - Complications - Diagnosis - Genetics | en_US |
dc.title | Diagnosis of concurrent hemoglobin H disease and heterozygous β-thalassemia [1] | en_US |
dc.type | Article | en_US |
dc.identifier.email | Chan, LC:chanlc@hkucc.hku.hk | en_US |
dc.identifier.authority | Chan, LC=rp00373 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.pmid | 11325652 | en_US |
dc.identifier.scopus | eid_2-s2.0-0035018158 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-0035018158&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 86 | en_US |
dc.identifier.issue | 4 | en_US |
dc.identifier.spage | 432 | en_US |
dc.identifier.epage | 433 | en_US |
dc.identifier.isi | WOS:000168303800018 | - |
dc.publisher.place | Italy | en_US |
dc.identifier.issnl | 0390-6078 | - |