Neonatal screening

BMJ

Volumn 312, Issue 7024, 1996, Pages 182-

  Cappuccio, Francesco P ^a   Hickman, Matthew ^a   Barker, Maggie ^a  

^a Brent and Harrow Health Authority   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

COUNSELING; HUMAN; INFORMED CONSENT; MEDICAL ETHICS; NEWBORN; NEWBORN SCREENING; NOTE; CONGENITAL HYPOTHYROIDISM; FAMILY COUNSELING; FOLLOW UP; LETTER; PHENYLKETONURIA; PRIMARY HEALTH CARE; PRIORITY JOURNAL;

COUNSELING; ETHICS, MEDICAL; HUMANS; INFANT, NEWBORN; INFORMED CONSENT; NEONATAL SCREENING;

EID: 0030594009     PISSN: 09598138     EISSN: 14685833     Source Type: Journal    
DOI: 10.1136/bmj.312.7024.182b     Document Type: Letter

References (4)

1. Streetly A, Grant C, Pollitt RJ, Addison GM. Survey of scope of neonatal screening in the United Kingdom. BMJ 1995; 311: 726. (16 September.).
2. Phaorah POD, Madden MP. Audit of screening for congenital hypothyroidism. Arch Dis Child 1992; 67: 1073–6.
3. Elliman D, Garner D. Review of neonatal screening programme for phenylketonuria. BMJ 1991; 303: 471.
4. Streetly A, Grant C, Bickler G, Eldridge P, Bird S, Griffiths W. Variation in coverage by ethnic group of neonatal (Guthrie) screening programme in south London. BMJ 1994; 309: 372–374.