Neonatal Screening for Sickle Cell Disorders: What About the Carrier Infants?
Anionwu, Elizabeth N.
BMJ (British Medical Journal). 1996 Aug 17; 313(7054): 404-411.
Costs and Benefits; Counseling; Carriers; Diagnosis; Disclosure; Education; Fathers; Genetic Screening; Health; Health Education; Health Personnel; Infants; Minority Groups; Newborns; Parent Child Relationship; Parents; Psychological Stress; Reproduction; Risks and Benefits; Sickle Cell Anemia; Stigmatization; Truth Disclosure; Uncertainty;
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