Neidio i'r cynnwys
VuFind
English
Deutsch
Español
Français
Italiano
日本語
Nederlands
Português
Português (Brasil)
中文(简体)
中文(繁體)
Türkçe
עברית
Gaeilge
Cymraeg
Ελληνικά
Català
Euskara
Русский
Čeština
Suomi
Svenska
polski
Dansk
slovenščina
اللغة العربية
বাংলা
Galego
Tiếng Việt
Hrvatski
हिंदी
Հայերէն
Українська
Sámegiella
Монгол
Iaith
Pob Maes
Teitl
Awdur
Pwnc
Rhif Galw
ISBN/ISSN
Tag
Canfod
Uwch
A 5-base pair deletion in the...
Dyfynnu hwn
Anfonwch hwn fel neges destun
E-bostio hwn
Argraffu
Allforio Cofnod
Allforio i RefWorks
Allforio i EndNoteWeb
Allforio i EndNote
Permanent link
A 5-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a 6-generation Arkansas kindred.
Manylion Llyfryddiaeth
Prif Awduron:
Mumm, S
,
Christie, P
,
Finnegan, P
,
Jones, J
,
Dixon, P
,
Pannett, A
,
Harding, B
,
Gottesman, G
,
Thakker, R
,
Whyte, M
Fformat:
Journal article
Cyhoeddwyd:
2000
Daliadau
Disgrifiad
Eitemau Tebyg
Dangos Staff
Eitemau Tebyg
A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred.
gan: Mumm, S, et al.
Cyhoeddwyd: (2000)
Characterization of two genes within the candidate region for X-linked spondyloepiphyseal dysplasia tarda.
gan: Mumm, S, et al.
Cyhoeddwyd: (1997)
Characterization of two genes within the candidate region for X-linked spondyloepiphyseal dysplasia tarda.
gan: Mumm, S, et al.
Cyhoeddwyd: (1997)
Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda.
gan: Christie, P, et al.
Cyhoeddwyd: (2001)
Clinical Diagnosis of X-Linked Spondyloepiphyseal Dysplasia Tarda and a Novel Missense Mutation in the Sedlin Gene (SEDL)
gan: Lei Kong, et al.
Cyhoeddwyd: (2018-01-01)