Syndrome diagnosis with single-nucleotide polymorphism (SNP) microarray
Matthew Edwards
(1, 2)
,
Sally Brescianini
(2)
,
Catherine Allgood
(1)
,
Michael Freelander
(1)
,
Richard Dunstan
(1)
,
Patrick Patradoon-Ho
(1)
,
Raymond Chin
(1)
,
Lucy Morgan
(3)
,
Tasnuba Pervez
(1)
,
Marie Legendre
(4)
,
Trent Burgess
(5)
,
Serge Amselem
(6, 4)
,
John Whitehall
(1)
1
Western Sydney University
2 CH - Campbelltown Hospital [New South Wales, Australia]
3 CRGH - Concord Repatriation General Hospital [Sydney, Australia]
4 CHU Trousseau [APHP]
5 VCGS - Victorian Clinical Genetics Services [Melbourne, VIC, Australia]
6 Physiopathologie des maladies génétiques d'expression pédiatrique
2 CH - Campbelltown Hospital [New South Wales, Australia]
3 CRGH - Concord Repatriation General Hospital [Sydney, Australia]
4 CHU Trousseau [APHP]
5 VCGS - Victorian Clinical Genetics Services [Melbourne, VIC, Australia]
6 Physiopathologie des maladies génétiques d'expression pédiatrique
Marie Legendre
- Fonction : Auteur
- PersonId : 1147534
- IdHAL : marie-legendre
- ORCID : 0000-0003-2178-0846
Serge Amselem
- Fonction : Auteur
- PersonId : 936326
- IdHAL : serge-amselem
- ORCID : 0000-0001-9506-3968
- IdRef : 066957761
Résumé
No abstract available