Prenatal diagnosis of a case with X-linked spondyloepiphyseal dysplasia tarda

Fang CAO; Qiu-wei WANG; Bin YU; Rui-ping HUANG; Ya-li HU; Xiao-qing ZHANG.
Chinese Journal of Medical Genetics ; (6): 598-600, 2013.
Artículo en Zh | WPRIM | ID: wpr-237198

Documentos relacionados

  1. You "Cantu": Multidisciplinary Collaboration Resulting in Successful Orthognathic Surgery.
  2. [Prenatal diagnosis of a case with X-linked spondyloepiphyseal dysplasia tarda].
  3. AIFM1-associated X-linked spondylometaphyseal dysplasia with cerebral hypomyelination.
  4. [Early prenatal diagnosis for a family affected with X-linked spondyloepiphyseal dysplasia tarda family].
  5. Surgical Management of Craniomaxillofacial Features in the Otopalatodigital Spectrum Disorders.
  6. Novel loss-of-function variants of TRAPPC2 manifesting X-linked spondyloepiphyseal dysplasia tarda: report of two cases.
  7. X-linked frontometaphyseal dysplasia with severe scoliosis and spinal cord compromise in an Indian boy.
  8. [Clinical and molecular genetic analysis of a child with Schmid type metaphyseal chondrodysplasia].
  9. A kilonova following a long-duration gamma-ray burst at 350 Mpc.
  10. DNA Methylation Status of SHOX-Flanking CpG Islands in Healthy Individuals and Short Stature Patients with Pseudoautosomal Copy Number Variations.