Lafrenière R G, Brown C J, Powers V E, Carrel L, Davies K E, Barker D F, Willard H F
Department of Genetics, Stanford University School of Medicine, California 94305.
Genomics. 1991 Oct;11(2):352-63. doi: 10.1016/0888-7543(91)90143-3.
Using a panel of human/rodent somatic cell hybrids and human lymphoblast lines segregating 18 different human X-chromosome rearrangements and deletions, we have assigned 60 DNA markers to the physical map of the X chromosome from Xp21.1 to Xq21.3. Data from Southern blot hybridization and polymerase chain reaction (PCR) amplification assign these markers to 15 primary map intervals. This provides a basis for further long-range cloning and mapping of the pericentromeric region of the X chromosome.