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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
1
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pubmed:dateCreated |
2011-1-3
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pubmed:abstractText |
Co-inheritance of ?- and ?-globin mutations in Iran is not uncommon. This situation may interfere with correct diagnosis and genetic counseling of ?- and ?-thalassemia in screening programs. Here we report the co-inheritance of ?- and ?-globin gene mutations in an individual with microcytosis, hypochromia and a normal hemoglobin A? (HbA?) level.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Jan
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pubmed:issn |
1029-2977
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
8-11
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pubmed:meshHeading |
pubmed-meshheading:21194254-Adult,
pubmed-meshheading:21194254-DNA Mutational Analysis,
pubmed-meshheading:21194254-Diagnosis, Differential,
pubmed-meshheading:21194254-Female,
pubmed-meshheading:21194254-Hemoglobin A2,
pubmed-meshheading:21194254-Hemoglobins, Abnormal,
pubmed-meshheading:21194254-Humans,
pubmed-meshheading:21194254-Inheritance Patterns,
pubmed-meshheading:21194254-Iran,
pubmed-meshheading:21194254-Male,
pubmed-meshheading:21194254-Mass Screening,
pubmed-meshheading:21194254-Middle Aged,
pubmed-meshheading:21194254-Point Mutation,
pubmed-meshheading:21194254-Polymerase Chain Reaction,
pubmed-meshheading:21194254-beta-Globins,
pubmed-meshheading:21194254-beta-Thalassemia,
pubmed-meshheading:21194254-delta-Globins,
pubmed-meshheading:21194254-delta-Thalassemia
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pubmed:year |
2011
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pubmed:articleTitle |
First report on the co-inheritance of beta-globin IVS-I-5 (G-->C) thalassemia with delta globin CD12 {Asn-->Lys (AAT-->AAA)}HbA?-NYU in Iran.
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pubmed:affiliation |
Molecular Medicine Department, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran.
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pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
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