Linkage studies do not confirm the cytogenetic location of incontinentia pigmenti on Xp11

Hum Genet. 1988 Nov;80(3):282-6. doi: 10.1007/BF01790098.

Abstract

Linkage studies have been performed in 5 incontinentia pigmenti (IP) families totaling 29 potentially informative meioses. Ten probes of the Xp arm were used, six of them were precisely localized on the X chromosome, using hamster X human somatic cell hybrids containing a broken X chromosome derived from an incontinentia pigmenti patient carrying an X;9 translocation [46,XX,t(X;9)(p11.21;q34)]. The following order for probes is proposed: pter - (DXS7, DXS146, DXS255) - IP1 - (DXS14, DXS90) - DXS106 - qter. The negative lod scores obtained exclude the possibility that in the families studied, the gene for IP is located in Xp11 or in the major part of the Xp arm.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromosome Mapping
  • Cricetinae
  • Cricetulus
  • DNA Probes
  • Female
  • Genetic Linkage*
  • Genetic Markers
  • Humans
  • Hybrid Cells
  • Incontinentia Pigmenti / genetics*
  • Male
  • Nucleic Acid Hybridization
  • Pedigree
  • Pigmentation Disorders / genetics*
  • X Chromosome*

Substances

  • DNA Probes
  • Genetic Markers