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Spondyloepimetaphyseal dysplasia with multiple dislocations (Hall type): three further cases and evidence of autosomal dominant inheritance

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dc.contributor.authorELÇİOĞLU, HURİYE NURSEL
dc.contributor.authorsHall, CM; Elcioglu, NH; MacDermot, KD; Offiah, AC; Winter, RM
dc.date.accessioned2022-03-14T10:04:36Z
dc.date.accessioned2026-01-11T15:08:45Z
dc.date.available2022-03-14T10:04:36Z
dc.date.issued2002-09-01
dc.identifier.doi10.1136/jmg.39.9.666
dc.identifier.issn0022-2593
dc.identifier.pubmed12205110
dc.identifier.urihttps://hdl.handle.net/11424/244009
dc.identifier.wosWOS:000178000700008
dc.language.isoeng
dc.publisherBRITISH MED JOURNAL PUBL GROUP
dc.relation.ispartofJOURNAL OF MEDICAL GENETICS
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectSPONASTRIME DYSPLASIA
dc.titleSpondyloepimetaphyseal dysplasia with multiple dislocations (Hall type): three further cases and evidence of autosomal dominant inheritance
dc.typearticle
dspace.entity.typePublication
oaire.citation.endPage670
oaire.citation.issue9
oaire.citation.startPage666
oaire.citation.titleJOURNAL OF MEDICAL GENETICS
oaire.citation.volume39

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