Alport syndrome, mental retardation, midface hypoplasia, and elliptocytosis: A new X linked contiguous gene deletion syndrome?

  1. Jonsson, J.J.
  2. Renieri, A.
  3. Gallagher, P.G.
  4. Kashtan, C.E.
  5. Cherniske, E.M.
  6. Bruttini, M.
  7. Piccini, M.
  8. Vitelli, F.
  9. Ballabio, A.
  10. Pober, B.R.
Revue:
Journal of Medical Genetics

ISSN: 0022-2593

Année de publication: 1998

Volumen: 35

Número: 4

Pages: 273-278

Type: Article

DOI: 10.1136/JMG.35.4.273 GOOGLE SCHOLAR lock_openAccès ouvert editor

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