Molecular Cytogenetic Evidence for a Common Breakpoint in the Largest Inverted Duplications of Chromosome 15

This publication has 40 references indexed in Scilit:

• EXTRA DICENTRIC 15pter→q21/22 CHROMOSOMES IN FIVE UNRELATED PATIENTS WITH A DISTINCT SYNDROME OF PROGRESSIVE PSYCHOMOTOR RETARDATION, SEIZURES, HYPER-REACTIVITY AND DERMATOGLYPHIC ABNORMALITIES
  Journal of Intellectual Disability Research, 2008
• Cytogenetic and molecular analysis of inv dup(15) chromosomes observed in two patients with autistic disorder and mental retardation
  American Journal of Medical Genetics, 1996
• Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11–q13
  American Journal of Medical Genetics, 1995
• A complete YAC contig of the Prader-Willi/Angelman chromosome region (15q11–q13) and refined localization of the SNRPN gene
  Genomics, 1993
• A linkage map of human chromosome 15 with an average resolution of 2 cM and containing 55 polymorphic microsatellites
  Human Molecular Genetics, 1993
• Clarification of subtle reciprocal rearrangements using fluorescence in situ hybridization
  American Journal of Medical Genetics, 1993
• Genomic imprinting and uniparental disomy in Angelman and Prader‐Willi syndromes: A review
  American Journal of Medical Genetics, 1993
• Regional localization of the gene for cardiac muscle actin (ACTC) on chromosome 15q
  Genomics, 1992
• Small marker chromosomes in man: origin from pericentric heterochromatin of chromosomes 1, 9, and 16.
  Journal of Medical Genetics, 1990
• Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader‐Willi syndrome
  American Journal of Medical Genetics, 1989