Definition of a Critical Region on Chromosome 18 for Congenital Aural Atresia by ArrayCGH

This publication has 24 references indexed in Scilit:

• Characterizing the physical genome
  Nature Genetics, 2002
• High-Throughput Analysis of Subtelomeric Chromosome Rearrangements by Use of Array-Based Comparative Genomic Hybridization
  The American Journal of Human Genetics, 2002
• Association of external auditory canal atresia, vertical talus, and hypertelorism: Confirmation of rasmussen syndrome
  American Journal of Medical Genetics, 2002
• SALL3, a New Member of the Human spalt-like Gene Family, Maps to 18q23
  Genomics, 1999
• Cloning and Characterization of ZNF236, a Glucose-Regulated Kruppel-like Zinc-Finger Gene Mapping to Human Chromosome 18q22–q23
  Genomics, 1999
• Analysis of clinical variation seen in patients with 18q terminal deletions
  American Journal of Medical Genetics, 1995
• Degenerate oligonucleotide-primed PCR: General amplification of target DNA by a single degenerate primer
  Genomics, 1992
• Segmental spinal muscular atrophy and dermatological findings in a patient with chromosome 18q deletion
  Annals of Neurology, 1991
• Interstitial deletion of the long arm of chromosome 18, del(18)(q12.2q21.1): a report of three cases of an autosomal deletion with a mild phenotype.
  Journal of Medical Genetics, 1991
• Syndromes associated with deletion of the long arm of chromosome 18[del(18q)]
  American Journal of Medical Genetics, 1979