Abstract DNA from a human-hamster hybrid cell line, 908-K1B17, containing a small terminal portion of the long arm of the human X chromosome as well as the pericentric region of 19q was used as starting material for the isolation of an X-chromosome-specific DNA segment, RN1 (DXS369), which identifies a XmnI RFLP. Linkage analysis in fragile X families resulted in a maximum lod score of 15.3 at a recombination fraction of 0.05 between RN1 and fra(X). Analysis of recombinations around the fra(X) locus assigned RN1 proximal to fra(X) and distal to DXS105. Analysis of the marker content of hybrid cell line 908K1B17 suggests the localization of RN1 between DXS98 and fra(X). Heterozygosity of DXS369 is approximately 50%, which extends the di...
Previously, we showed genetic heterogeneity for linkage between the fra(X) locus and a factor IX DNA...
Genetic linkage between a factor IX DNA restriction fragment length polymorphism (RFLP) and the frag...
Of the seven folate-sensitive fragile sites cloned in the human genome, only two have a proven clini...
We have isolated II-10, a new X-chromosomal probe that identifies a highly informative two-allele Ta...
textabstractWe have isolated II-10, a new X-chromosomal probe that identifies a highly informative t...
al probe that identifies a highly informative two-allele TaqI restriction fragment length polymorphi...
The X chromosome is probably the most studied of all human chromosomes, in part because more than 11...
The Fragile X Syndrome is the most common cause of heritable mental retardation, affecting one in 20...
The q26-q28 region of the human X chromosome contains several important disease loci, including the ...
The fragile X syndrome (FraX), the most common inherited form of mental retardation, has been locate...
The fragile X syndrome (FraX), the most common inherited form of mental retardation, has been locate...
The fragile X syndrome (FraX), the most common inherited form of mental retardation, has been locate...
Conclusion Rapid progress has been made in the analysis of the fragile X syndrome during 1991. Di...
The X-linked fragile X [fra(X)] syndrome, associated with a fragile site at Xq27.3, is the most comm...
Abstract Fragile X syndrome, the most common inherited form of mental retardation syndrome, is cause...
Previously, we showed genetic heterogeneity for linkage between the fra(X) locus and a factor IX DNA...
Genetic linkage between a factor IX DNA restriction fragment length polymorphism (RFLP) and the frag...
Of the seven folate-sensitive fragile sites cloned in the human genome, only two have a proven clini...
We have isolated II-10, a new X-chromosomal probe that identifies a highly informative two-allele Ta...
textabstractWe have isolated II-10, a new X-chromosomal probe that identifies a highly informative t...
al probe that identifies a highly informative two-allele TaqI restriction fragment length polymorphi...
The X chromosome is probably the most studied of all human chromosomes, in part because more than 11...
The Fragile X Syndrome is the most common cause of heritable mental retardation, affecting one in 20...
The q26-q28 region of the human X chromosome contains several important disease loci, including the ...
The fragile X syndrome (FraX), the most common inherited form of mental retardation, has been locate...
The fragile X syndrome (FraX), the most common inherited form of mental retardation, has been locate...
The fragile X syndrome (FraX), the most common inherited form of mental retardation, has been locate...
Conclusion Rapid progress has been made in the analysis of the fragile X syndrome during 1991. Di...
The X-linked fragile X [fra(X)] syndrome, associated with a fragile site at Xq27.3, is the most comm...
Abstract Fragile X syndrome, the most common inherited form of mental retardation syndrome, is cause...
Previously, we showed genetic heterogeneity for linkage between the fra(X) locus and a factor IX DNA...
Genetic linkage between a factor IX DNA restriction fragment length polymorphism (RFLP) and the frag...
Of the seven folate-sensitive fragile sites cloned in the human genome, only two have a proven clini...