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Volumn 120 Suppl 2, Issue , 2007, Pages
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Linking family history in obstetric and pediatric care: assessing risk for genetic disease and birth defects.
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Author keywords
[No Author keywords available]
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Indexed keywords
ADULT;
ANAMNESIS;
CHILD;
CLASSIFICATION;
CONGENITAL MALFORMATION;
DEVELOPMENTAL DISORDER;
FAMILY HEALTH;
FEMALE;
GENETIC DISORDER;
GENETIC PREDISPOSITION;
GENETIC SCREENING;
GENETICS;
HUMAN;
MALE;
METHODOLOGY;
NEWBORN;
OBSTETRICS;
ORGANIZATION AND MANAGEMENT;
PEDIATRICS;
PEDIGREE;
PREGNANCY;
PREGNANCY COMPLICATION;
PRENATAL CARE;
PRIMARY HEALTH CARE;
REVIEW;
RISK ASSESSMENT;
UNITED STATES;
ABNORMALITIES;
ADULT;
CHILD;
DEVELOPMENTAL DISABILITIES;
FAMILY HEALTH;
FEMALE;
GENETIC DISEASES, INBORN;
GENETIC PREDISPOSITION TO DISEASE;
GENETIC SCREENING;
HUMANS;
INFANT, NEWBORN;
MALE;
MEDICAL HISTORY TAKING;
OBSTETRICS;
PEDIATRICS;
PEDIGREE;
PREGNANCY;
PREGNANCY COMPLICATIONS;
PRENATAL CARE;
PRIMARY HEALTH CARE;
RISK ASSESSMENT;
UNITED STATES;
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EID: 34548554401
PISSN: None
EISSN: 10984275
Source Type: Journal
DOI: 10.1542/peds.2007-1010E Document Type: Review |
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Times cited : (31)
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References (20)
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