Another patient with cryptic unbalanced translocation between chromosomes 4q and 18q: Evidence by microarray CGH

This publication has 15 references indexed in Scilit:

• Molecular characterization of a patient with central nervous system dysmyelination and cryptic unbalanced translocation between chromosomes 4q and 18q
  American Journal of Medical Genetics Part A, 2003
• Association of external auditory canal atresia, vertical talus, and hypertelorism: Confirmation of rasmussen syndrome
  American Journal of Medical Genetics, 2002
• Scanning for telomeric deletions and duplications and uniparental disomy using genetic markers in 120 children with malformations
  Human Genetics, 2001
• Identification of Cryptic Rearrangements in Patients with 18q− Deletion Syndrome
  American Journal of Human Genetics, 1998
• Mutations in the SALL1 putative transcription factor gene cause Townes-Brocks syndrome
  Nature Genetics, 1998
• Analysis of clinical variation seen in patients with 18q terminal deletions
  American Journal of Medical Genetics, 1995
• Segmental spinal muscular atrophy and dermatological findings in a patient with chromosome 18q deletion
  Annals of Neurology, 1991
• Localization of the human myelin basic protein gene (MBP) to region 18q22→qter by in situ hybridization
  Cytogenetic and Genome Research, 1985
• Inherited Congenital Bilateral Atresia of the External Auditory Canal, Congenital Bilateral Vertical Talus and Increased Interocular Distance
  Acta Oto-Laryngologica, 1979
• Clinical and chromosomal studies of the 18q-syndrome
  The Journal of Pediatrics, 1971