Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2009-11-30
pubmed:abstractText
Deletions in the beta-globin cluster causing thalassaemia and hereditary persistence of fetal haemoglobin (HPFH) are uncommon and difficult to detect. Data in Chinese are very scarce.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
AIM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
1472-4146
pubmed:author
pubmed:issnType
Electronic
pubmed:volume
62
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
1107-11
pubmed:meshHeading
pubmed-meshheading:19946097-Adolescent, pubmed-meshheading:19946097-Adult, pubmed-meshheading:19946097-Aged, pubmed-meshheading:19946097-Aged, 80 and over, pubmed-meshheading:19946097-Asian Continental Ancestry Group, pubmed-meshheading:19946097-Child, pubmed-meshheading:19946097-Child, Preschool, pubmed-meshheading:19946097-Female, pubmed-meshheading:19946097-Fetal Hemoglobin, pubmed-meshheading:19946097-Gene Deletion, pubmed-meshheading:19946097-Genotype, pubmed-meshheading:19946097-Hemoglobinopathies, pubmed-meshheading:19946097-Humans, pubmed-meshheading:19946097-Infant, pubmed-meshheading:19946097-Male, pubmed-meshheading:19946097-Middle Aged, pubmed-meshheading:19946097-Multigene Family, pubmed-meshheading:19946097-Nucleic Acid Amplification Techniques, pubmed-meshheading:19946097-Phenotype, pubmed-meshheading:19946097-Thalassemia, pubmed-meshheading:19946097-Young Adult, pubmed-meshheading:19946097-beta-Globins, pubmed-meshheading:19946097-beta-Thalassemia
pubmed:year
2009
pubmed:articleTitle
Detection and characterisation of beta-globin gene cluster deletions in Chinese using multiplex ligation-dependent probe amplification.
pubmed:affiliation
Department of Pathology, Li Ka Shing Faculty of Medicine, University of Hong Kong, Hong Kong SAR, China. scc@pathology.hku.hk
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't