Probes for CpG islands were cloned from the distal long arm of the human X chromosome; three of them were found to be polymorphic. A HindIII RFLP was identified by the probe 2-25 (DXS606), and it was mapped to the Xq27-Xq28 boundary. Probes 2-19 (DXS605) and 2-55 (DXS707), which identify EcoRI and MspI polymorphisms, respectively, have been mapped to the distal part of Xq28, in the G6PD-RCP/GCP gene region. Probe 2-19 has been further localized about 16 kb from the 3' end of the G6PD gene. The new RFLPs may be useful for the precise mapping of the many disease genes localized in this part of the human X chromosome. Probe 2-19 is highly informative, and it has been studied in greater detail. Using the methylation-sensitive rare-cutter enzyme...
X-linked agammaglobulinemia is a primary immunodeficiency which arises as a result of a block in B c...
Retinitis Pigmentosa (RP) is an inherited disease of the retina, in which progressive degeneration o...
The process of X-chromosome inactivation achieves dosage compensation between mammalian males and fe...
Probes for CpG islands were cloned from the distal long arm of the human X chromosome; three of them...
The isolation and characterization of DNA probes which detect RFLPs from a small region of the human...
We have isolated and characterized 55 EagI-containing genomic DNA clones from the distal long arm of...
In a search for highly polymorphic X-specific loci, the X-chromosome DOE Ch35 phage library (LAOXNL0...
The X chromosome is probably the most studied of all human chromosomes, in part because more than 11...
Several genes involved in human genetic diseases map to the Xq22 band on the long arm of the human X...
The q26-q28 region of the human X chromosome contains several important disease loci, including the ...
dissertationThe genetic mapping of many X-linked disease genes has been hindered by the uninformativ...
X-linked agammaglobulinemia (XLA) is an inherited immunodeficiency disease which results in a defici...
The gene for X-linked agammaglobulinemia (XLA) has been mapped to Xq22. No recombinations have been ...
International audienceA repeated DNA element (STIR) interspersed in Xp22.3 and on the Y chromosome h...
Two males and two females with different but overlapping deletions on the proximal long arm of the X...
X-linked agammaglobulinemia is a primary immunodeficiency which arises as a result of a block in B c...
Retinitis Pigmentosa (RP) is an inherited disease of the retina, in which progressive degeneration o...
The process of X-chromosome inactivation achieves dosage compensation between mammalian males and fe...
Probes for CpG islands were cloned from the distal long arm of the human X chromosome; three of them...
The isolation and characterization of DNA probes which detect RFLPs from a small region of the human...
We have isolated and characterized 55 EagI-containing genomic DNA clones from the distal long arm of...
In a search for highly polymorphic X-specific loci, the X-chromosome DOE Ch35 phage library (LAOXNL0...
The X chromosome is probably the most studied of all human chromosomes, in part because more than 11...
Several genes involved in human genetic diseases map to the Xq22 band on the long arm of the human X...
The q26-q28 region of the human X chromosome contains several important disease loci, including the ...
dissertationThe genetic mapping of many X-linked disease genes has been hindered by the uninformativ...
X-linked agammaglobulinemia (XLA) is an inherited immunodeficiency disease which results in a defici...
The gene for X-linked agammaglobulinemia (XLA) has been mapped to Xq22. No recombinations have been ...
International audienceA repeated DNA element (STIR) interspersed in Xp22.3 and on the Y chromosome h...
Two males and two females with different but overlapping deletions on the proximal long arm of the X...
X-linked agammaglobulinemia is a primary immunodeficiency which arises as a result of a block in B c...
Retinitis Pigmentosa (RP) is an inherited disease of the retina, in which progressive degeneration o...
The process of X-chromosome inactivation achieves dosage compensation between mammalian males and fe...