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Volumn 132, Issue 2, 2006, Pages 249-250
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Human transferrin G277S mutation and iron deficiency in pregnancy [4]
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Author keywords
Iron deficiency; Pregnancy
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Indexed keywords
FERRITIN;
HEMOGLOBIN;
IRON;
TRANSFERRIN;
TRANSFERRIN RECEPTOR;
CONTROLLED STUDY;
DNA POLYMORPHISM;
FEMALE;
FERRITIN BLOOD LEVEL;
FIRST TRIMESTER PREGNANCY;
GENE FREQUENCY;
GENE MUTATION;
GENE SEQUENCE;
GENETIC RISK;
GENOTYPE;
HEMATOCRIT;
HEMOGLOBIN BLOOD LEVEL;
HUMAN;
IRON BLOOD LEVEL;
IRON DEFICIENCY ANEMIA;
IRON METABOLISM;
LETTER;
MAJOR CLINICAL STUDY;
PREGNANCY;
PRIORITY JOURNAL;
RISK ASSESSMENT;
SECOND TRIMESTER PREGNANCY;
THIRD TRIMESTER PREGNANCY;
TRANSFERRIN BLOOD LEVEL;
ADULT;
GENETIC PREDISPOSITION;
GENETICS;
MUTATION;
PREGNANCY COMPLICATION;
ADULT;
ANEMIA, IRON-DEFICIENCY;
FEMALE;
GENETIC PREDISPOSITION TO DISEASE;
HUMANS;
MUTATION;
PREGNANCY;
PREGNANCY COMPLICATIONS, HEMATOLOGIC;
TRANSFERRIN;
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EID: 33644828739
PISSN: 00071048
EISSN: 13652141
Source Type: Journal
DOI: 10.1111/j.1365-2141.2005.05871.x Document Type: Letter |
Times cited : (11)
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References (6)
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