File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: towards recommendation for molecular testing and management

DC FieldValueLanguage
dc.contributor.authorAvila, M-
dc.contributor.authorDyment, DA-
dc.contributor.authorSagen, JV-
dc.contributor.authorSt-Onge, J-
dc.contributor.authorMoog, U-
dc.contributor.authorChung, BHY-
dc.contributor.authorMansour, S-
dc.contributor.authorAlbanese, A-
dc.contributor.authorGarcia,, S-
dc.contributor.authorOrtiz Martin, D-
dc.contributor.authorLopez, AA-
dc.contributor.authorClaudi, T-
dc.contributor.authorKönig, R-
dc.contributor.authorWhite, SM-
dc.contributor.authorSawyer, SL-
dc.contributor.authorBernstein, JA-
dc.contributor.authorSlattery, L-
dc.contributor.authorJobling, RK-
dc.contributor.authorYoon, G-
dc.contributor.authorCurry, CJ-
dc.contributor.authorLe Merrer, M-
dc.contributor.authorLe Luyer, B-
dc.contributor.authorHéron, D-
dc.contributor.authorMathieu-Dramard, M-
dc.contributor.authorBitoun, P-
dc.contributor.authorOdent, S-
dc.contributor.authorAmiel, J-
dc.contributor.authorKuentz, P-
dc.contributor.authorThevenon, J-
dc.contributor.authorLaville, M-
dc.contributor.authorReznik, Y-
dc.contributor.authorFagour, C-
dc.contributor.authorNunes, ML-
dc.contributor.authorDelesalle, D-
dc.contributor.authorManouvrier, S-
dc.contributor.authorLascols, O-
dc.contributor.authorHuet, F-
dc.contributor.authorBinquet, C-
dc.contributor.authorFaivre, L-
dc.contributor.authorRivière, JB-
dc.contributor.authorVigouroux, C-
dc.contributor.authorNjølstad, PR-
dc.contributor.authorInnes, AC-
dc.contributor.authorThauvin-Robinet, C-
dc.date.accessioned2015-12-21T05:47:11Z-
dc.date.available2015-12-21T05:47:11Z-
dc.date.issued2015-
dc.identifier.citationClinical Genetics, 2015-
dc.identifier.urihttp://hdl.handle.net/10722/221906-
dc.languageeng-
dc.relation.ispartofClinical Genetics-
dc.titleClinical reappraisal of SHORT syndrome with PIK3R1 mutations: towards recommendation for molecular testing and management -
dc.typeArticle-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.authorityChung, BHY=rp00473-
dc.identifier.doi10.1111/cge.12688-
dc.identifier.hkuros256461-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats