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Spondyloepiphyseal dysplasia, Omani type: further definition of the phenotype.
van Roij, Mirjam H H; Mizumoto, Shuji; Yamada, Shuhei; Morgan, Tim; Tan-Sindhunata, M B; Meijers-Heijboer, H; Verbeke, J I L M; Markie, David; Sugahara, Kazuyuki; Robertson, Stephen P.
Affiliation
  • van Roij MH; Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands.
Am J Med Genet A ; 146A(18): 2376-84, 2008 Sep 15.
Article in En | MEDLINE | ID: mdl-18698629
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteochondrodysplasias / Sulfotransferases / Point Mutation Type of study: Diagnostic_studies Limits: Child / Child, preschool / Female / Humans Country/Region as subject: Asia Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2008 Document type: Article Affiliation country: Netherlands
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteochondrodysplasias / Sulfotransferases / Point Mutation Type of study: Diagnostic_studies Limits: Child / Child, preschool / Female / Humans Country/Region as subject: Asia Language: En Journal: Am J Med Genet A Journal subject: GENETICA MEDICA Year: 2008 Document type: Article Affiliation country: Netherlands