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Article: Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations

TitleVariable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations
Authors
Issue Date2016
PublisherBMJ Group. The Journal's web site is located at http://jmg.bmj.com/
Citation
Journal of Medical Genetics, 2016, v. 53 n. 6, p. 427-430 How to Cite?
Persistent Identifierhttp://hdl.handle.net/10722/221903
ISSN
2021 Impact Factor: 5.941
2020 SCImago Journal Rankings: 2.439
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorAldinger, KA-
dc.contributor.authorMendelsohn, NJ-
dc.contributor.authorChung, BHY-
dc.contributor.authorZhang, W-
dc.contributor.authorCohn, DH-
dc.contributor.authorFernandez, B-
dc.contributor.authorAlkuraya, FS-
dc.contributor.authorDobyns, WB-
dc.contributor.authorCurry, CJ-
dc.date.accessioned2015-12-21T05:47:06Z-
dc.date.available2015-12-21T05:47:06Z-
dc.date.issued2016-
dc.identifier.citationJournal of Medical Genetics, 2016, v. 53 n. 6, p. 427-430-
dc.identifier.issn0022-2593-
dc.identifier.urihttp://hdl.handle.net/10722/221903-
dc.languageeng-
dc.publisherBMJ Group. The Journal's web site is located at http://jmg.bmj.com/-
dc.relation.ispartofJournal of Medical Genetics-
dc.rightsJournal of Medical Genetics. Copyright © BMJ Group.-
dc.titleVariable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations-
dc.typeArticle-
dc.identifier.emailChung, BHY: bhychung@hku.hk-
dc.identifier.authorityChung, BHY=rp00473-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1136/jmedgenet-2015-103476-
dc.identifier.scopuseid_2-s2.0-84974808948-
dc.identifier.hkuros256455-
dc.identifier.volume53-
dc.identifier.issue6-
dc.identifier.spage427-
dc.identifier.epage430-
dc.identifier.isiWOS:000377110800009-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl0022-2593-

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