Linkage of infantile Bartter syndrome with sensorineural deafness to chromosome 1p.

Podobne zapisy

• A Bedouin kindred with infantile nephronophthisis demonstrates linkage to chromosome 9 by homozygosity mapping.
  od: Haider, N B, i wsp.
  Wydane: (1998)
• Antenatal Bartter's syndrome with sensorineural deafness
  od: Bhamkar, R. P., i wsp.
  Wydane: (2009)
• Homozygosity and linkage-disequilibrium mapping of the syndrome of congenital hypoparathyroidism, growth and mental retardation, and dysmorphism to a 1-cM interval on chromosome 1q42-43.
  od: Parvari, R, i wsp.
  Wydane: (1998)
• Lipomatous myelomeningocele, athyrotic hypothyroidism, and sensorineural deafness: a new form of syndromal deafness?
  od: Peters, H L, i wsp.
  Wydane: (1998)
• Autozygosity mapping, to chromosome 11q25, of a rare autosomal recessive syndrome causing histiocytosis, joint contractures, and sensorineural deafness.
  od: Moynihan, L M, i wsp.
  Wydane: (1998)