Genetic Interaction of BBS1 Mutations with Alleles at Other BBS Loci Can Result in Non-Mendelian Bardet-Biedl Syndrome

Lignende værker

• BBS4 Is a Minor Contributor to Bardet-Biedl Syndrome and May Also Participate in Triallelic Inheritance
  af: Katsanis, Nicholas, et al.
  Udgivet: (2002)
• Identification of a Novel Bardet-Biedl Syndrome Protein, BBS7, That Shares Structural Features with BBS1 and BBS2
  af: Badano, José L., et al.
  Udgivet: (2003)
• Genetic and Mutational Analyses of a Large Multiethnic Bardet-Biedl Cohort Reveal a Minor Involvement of BBS6 and Delineate the Critical Intervals of Other Loci
  af: Beales, Philip L., et al.
  Udgivet: (2001)
• Bardet–Biedl syndrome
  af: Forsythe, Elizabeth, et al.
  Udgivet: (2013)
• Delineation of the Critical Interval of Bardet-Biedl Syndrome 1 (BBS1) to a Small Region of 11q13, through Linkage and Haplotype Analysis of 91 Pedigrees
  af: Katsanis, Nicholas, et al.
  Udgivet: (1999)