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

The commonest autosomal deletion, 22q11.2 deletion syndrome (22q11DS) is a multisystem disorder varying greatly in severity and age of identification between affected individuals. Holistic care is best served by a multidisciplinary team, with an anticipatory approach. Priorities tend to change with...

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Detalles Bibliográficos
Autores principales: Habel, Alex, Herriot, Richard, Kumararatne, Dinakantha, Allgrove, Jeremy, Baker, Kate, Baxendale, Helen, Bu’Lock, Frances, Firth, Helen, Gennery, Andrew, Holland, Anthony, Illingworth, Claire, Mercer, Nigel, Pannebakker, Merel, Parry, Andrew, Roberts, Anne, Tsai-Goodman, Beverly
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032642/
https://www.ncbi.nlm.nih.gov/pubmed/24384789
http://dx.doi.org/10.1007/s00431-013-2240-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032642/
https://www.ncbi.nlm.nih.gov/pubmed/24384789
http://dx.doi.org/10.1007/s00431-013-2240-z

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