Linkage of congenital recessive deafness (gene DFNB10) to chromosome 21q22.3.

Eitemau Tebyg

• Mutations of MYO6 Are Associated with Recessive Deafness, DFNB37
  gan: Ahmed, Zubair M., et al.
  Cyhoeddwyd: (2003)
• A Novel Autosomal Recessive Nonsyndromic Hearing Impairment Locus (DFNB42) Maps to Chromosome 3q13.31-q22.3
  gan: Aslam, Muhammad, et al.
  Cyhoeddwyd: (2005)
• Novel mutations of TMPRSS3 in four DFNB8/B10 families segregating congenital autosomal recessive deafness
  gan: Ben-Yosef, T., et al.
  Cyhoeddwyd: (2001)
• A Recessive Mendelian Model to Predict Carrier Probabilities of DFNB1 for Nonsyndromic Deafness
  gan: González, Juan R., et al.
  Cyhoeddwyd: (2006)
• Genetic Linkage Analysis of DFNB3, DFNB9 and DFNB21 Loci in GJB2 Negative Families with Autosomal Recessive Non-syndromic Hearing Loss
  gan: MASOUDI, Marjan, et al.
  Cyhoeddwyd: (2016)