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A 5-base pair deletion in the...
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A 5-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a 6-generation Arkansas kindred.
Bibliografske podrobnosti
Main Authors:
Mumm, S
,
Christie, P
,
Finnegan, P
,
Jones, J
,
Dixon, P
,
Pannett, A
,
Harding, B
,
Gottesman, G
,
Thakker, R
,
Whyte, M
Format:
Journal article
Izdano:
2000
Zaloga
Opis
Podobne knjige/članki
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A five-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a six-generation Arkansas kindred.
od: Mumm, S, et al.
Izdano: (2000)
Characterization of two genes within the candidate region for X-linked spondyloepiphyseal dysplasia tarda.
od: Mumm, S, et al.
Izdano: (1997)
Characterization of two genes within the candidate region for X-linked spondyloepiphyseal dysplasia tarda.
od: Mumm, S, et al.
Izdano: (1997)
Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda.
od: Christie, P, et al.
Izdano: (2001)
Clinical Diagnosis of X-Linked Spondyloepiphyseal Dysplasia Tarda and a Novel Missense Mutation in the Sedlin Gene (SEDL)
od: Lei Kong, et al.
Izdano: (2018-01-01)