LINKAGE STUDIES IN A KINDRED WITH AUTOSOMAL-DOMINANT SPONDYLOEPIMETAPHYSEAL DYSPLASIA (SEMD) INDICATE GENETIC-HETEROGENEITY

Slični predmeti

• Linkage studies of a Missouri kindred with autosomal dominant spondyloepimetaphyseal dysplasia (SEMD) indicate genetic heterogeneity.
  od: Gertner, J, i dr.
  Izdano: (1997)
• MMP13 mutation causes spondyloepimetaphyseal dysplasia, Missouri type (SEMD(MO).
  od: Kennedy, A, i dr.
  Izdano: (2005)
• IPSC reprogramming of two patients with spondyloepimetaphyseal dysplasia (SEMD, biglycan type)
  od: Pauline De Kinderen, i dr.
  Izdano: (2023-03-01)
• LINKAGE STUDIES IN A KINDRED WITH HYPOCALCIURIC HYPERCALCEMIA AND INCREASING SERUM PARATHYROID-HORMONE LEVELS INDICATE GENETIC-HETEROGENEITY
  od: Trump, D, i dr.
  Izdano: (1993)
• LINKAGE STUDIES IN A KINDRED FROM OKLAHOMA WITH FAMILIAL BENIGN HYPOCALCIURIC HYPERCALCEMIA (FBH) INDICATE GENETIC-HETEROGENEITY AND A 3RD LOCUS FOR FBH
  od: Trump, D, i dr.
  Izdano: (1995)