A 5-base pair deletion in the sedlin gene causes spondyloepiphyseal dysplasia tarda in a 6-generation Arkansas kindred.
Glavni autori: | Mumm, S, Christie, P, Finnegan, P, Jones, J, Dixon, P, Pannett, A, Harding, B, Gottesman, G, Thakker, R, Whyte, M |
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Format: | Journal article |
Izdano: |
2000
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Slični predmeti
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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, i dr.
Izdano: (2000) -
Characterization of two genes within the candidate region for X-linked spondyloepiphyseal dysplasia tarda.
od: Mumm, S, i dr.
Izdano: (1997) -
Characterization of two genes within the candidate region for X-linked spondyloepiphyseal dysplasia tarda.
od: Mumm, S, i dr.
Izdano: (1997) -
Mutational analysis in X-linked spondyloepiphyseal dysplasia tarda.
od: Christie, P, i dr.
Izdano: (2001) -
Clinical Diagnosis of X-Linked Spondyloepiphyseal Dysplasia Tarda and a Novel Missense Mutation in the Sedlin Gene (SEDL)
od: Lei Kong, i dr.
Izdano: (2018-01-01)