Physical mapping in the region of human Xq12-21.1 using pulsed field gel electrophoresis

[1]  S. Malcolm,et al.  Pulsed-field gel electrophoresis and radiation hybrid mapping analyses enable the ordering of eleven DNA loci in Xq22. , 1993, Genomics.

[2]  M. Conley X-linked severe combined immunodeficiency. , 1991, Clinical immunology and immunopathology.

[3]  H. Willard,et al.  Physical mapping of 60 DNA markers in the p21.1----q21.3 region of the human X chromosome. , 1991, Genomics.

[4]  H. Willard,et al.  An 18-locus linkage map of the pericentromeric region of the human X chromosome: genetic framework for mapping X-linked disorders. , 1991, Genomics.

[5]  A. Monaco,et al.  Report of the committee on the genetic constitution of the X chromosome (Part 1 of 7) , 1991 .

[6]  T. Glover,et al.  Localization of the translocation breakpoint in a female with Menkes syndrome to Xq13.2-q13.3 proximal to PGK-1. , 1991, American journal of human genetics.

[7]  F. Cremers,et al.  Molecular analysis of male-viable deletions and duplications allows ordering of 52 DNA probes on proximal Xq. , 1988, American journal of human genetics.

[8]  R. Nussbaum,et al.  Report of the committee on the genetic constitution of the X chromosome. , 1988, Cytogenetics and cell genetics.

[9]  P. Harper,et al.  Recognition and reanalysis of a cell line from a manifesting female with X linked hypohidrotic ectodermal dysplasia and an X; autosome balanced translocation. , 1988, Journal of medical genetics.

[10]  D. Page,et al.  Regional localization of polymorphic DNA loci on the proximal long arm of the X chromosome using deletions associated with choroideremia , 1988, Human Genetics.

[11]  A. Feinberg,et al.  A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. , 1983, Analytical biochemistry.

[12]  R. Nussbaum,et al.  Physical fine mapping of the choroideremia locus using Xq21 deletions associated with complex syndromes. , 1989, Genomics.

[13]  R. Nussbaum,et al.  Report of the committee on the genetic constitution of the X chromosome. , 1988, Cytogenetics and cell genetics.

[14]  A. Feinberg,et al.  "A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity". Addendum. , 1984, Analytical biochemistry.