The Gene for Pendred Syndrome Is Located between D7S501 and D7S692 in a 1.7-cM Region on Chromosome 7q

This publication has 19 references indexed in Scilit:

• Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4
  Nature Genetics, 1996
• A comprehensive genetic map of the human genome based on 5,264 microsatellites
  Nature, 1996
• Linkage of congenital, recessive deafness (DFNB4) to chromosome 7q31 and evidence for genetic heterogeneity in the Middle Eastern Druze population
  Human Molecular Genetics, 1995
• Pendred's Syndrome
  Annals of Otology, Rhinology & Laryngology, 1993
• Optimization of Microsatellite Analysis for Genetic Mapping
  Genomics, 1993
• Studies on the Thyroidal Defect in an Atypical Form of Pendred's Syndrome*
  Journal of Clinical Endocrinology & Metabolism, 1975
• Normal Peroxidase Activity in Pendred's Syndrome
  Journal of Clinical Endocrinology & Metabolism, 1973
• Fifteen Cases of Pendred's Syndrome: Congenital Deafness and Sporadic Goiter
  JAMA Otolaryngology–Head & Neck Surgery, 1972
• Association of congenital deafness with goitre (Pendred's syndrome): A study of 207 families
  Annals of Human Genetics, 1964
• Deafness with Sporadic Goiter: Pendred's Syndrome
  JAMA Otolaryngology–Head & Neck Surgery, 1962