Towards a safety net for management of 22q11.2 deletion syndrome: Guidelines for our times

European Journal of Pediatrics

Volumn 173, Issue 6, 2014, Pages 757-765

  Habel, Alex ^a   Herriot, Richard ^b   Kumararatne, Dinakantha ^c   Allgrove, Jeremy ^d   Baker, Kate ^c   Baxendale, Helen ^e   Bu'Lock, Frances ^f   Firth, Helen ^g   Gennery, Andrew ^h   Holland, Anthony ⁱ   Illingworth, Claire ^c   Mercer, Nigel ^j   Pannebakker, Merel ⁱ   Parry, Andrew ^k   Roberts, Anne ^l   Tsai Goodman, Beverly ^k  

^a CLEFT LIP AND PALATE ASSOCIATION   (United Kingdom)

^b ABERDEEN ROYAL INFIRMARY   (United Kingdom)

^c ADDENBROOKE S HOSPITAL   (United Kingdom)

^d BARTS HEALTH NHS TRUST   (United Kingdom)

^e PAPWORTH HOSPITAL   (United Kingdom)

^f GLENFIELD HOSPITAL   (United Kingdom)

^g CAMBRIDGE UNIVERSITY HOSPITALS NHS FOUNDATION TRUST   (United Kingdom)

^h Newcastle Upon Tyne Hospitals NHS Foundation Trust   (United Kingdom)

ⁱ UNIVERSITY OF CAMBRIDGE   (United Kingdom)

^j FRENCHAY HOSPITAL   (United Kingdom)

^k BRISTOL ROYAL HOSPITAL FOR CHILDREN   (United Kingdom)

^l NORTH BRISTOL NHS TRUST   (United Kingdom)

more..

Author keywords

22q11 deletion syndrome; Congenital abnormalities; Di George; Guidelines; Resource management; Velocardiofacial

Indexed keywords

ARTICLE; AUTOIMMUNE DISEASE; CHILD GROWTH; CHROMOSOME DELETION 22Q11; CONGENITAL HEART MALFORMATION; EARLY INTERVENTION; FEEDING DIFFICULTY; FETUS MALFORMATION; HUMAN; HYPOCALCEMIA; INTERPERSONAL COMMUNICATION; LEARNING; MENTAL HEALTH; MONITORING; PRACTICE GUIDELINE; PRIORITY JOURNAL; CHILD; CHROMOSOME 22; DIGEORGE SYNDROME; GENETICS; PATIENT CARE; PRESCHOOL CHILD;

CHILD; CHILD, PRESCHOOL; CHROMOSOMES, HUMAN, PAIR 22; DIGEORGE SYNDROME; HUMANS; PATIENT CARE TEAM;

EID: 84903817078     PISSN: 03406199     EISSN: 14321076     Source Type: Journal    
DOI: 10.1007/s00431-013-2240-z     Document Type: Article

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