We have isolated II-10, a new X-chromosomal probe that identifies a highly informative two-allele TaqI restriction fragment length polymorphism at locus DXS466. Using somatic cell hybrids containing distinct portions of the long arm of the X chromosome, we could localize DXS466 between DXS296 and DXS304, both of which are closely linked distal markers for fragile X. This regional localization was supported by the analysis, in fragile X families, of recombination events between these three loci, the fragile X locus and locus DXS52, the latter being located at a more distal position. DXS466 is closely linked to the fragile X locus with a peak lod score of 7.79 at a recombination fraction of 0.02. Heterozygosity of DXS466 is approximately 50%....
A panel of somatic cell hybrids and X-linked hypohidrotic ectodermal dysplasia (EDA) patient-derived...
The human gene for glucose-6-phosphate dehydrogenase (G6PD) has been subregionally mapped to band Xq...
Fragile X syndrome is now a well established common clinical entity and most of those who are aware ...
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...
Abstract DNA from a human-hamster hybrid cell line, 908-K1B17, containing a small terminal port...
The q26-q28 region of the human X chromosome contains several important disease loci, including the ...
The X chromosome is probably the most studied of all human chromosomes, in part because more than 11...
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...
The Fragile X Syndrome is the most common cause of heritable mental retardation, affecting one in 20...
Conclusion Rapid progress has been made in the analysis of the fragile X syndrome during 1991. Di...
A panel of somatic cell hybrids and X-linked hypohidrotic ectodermal dysplasia (EDA) patient-derived...
The human gene for glucose-6-phosphate dehydrogenase (G6PD) has been subregionally mapped to band Xq...
A panel of somatic cell hybrids and X-linked hypohidrotic ectodermal dysplasia (EDA) patient-derived...
The human gene for glucose-6-phosphate dehydrogenase (G6PD) has been subregionally mapped to band Xq...
Fragile X syndrome is now a well established common clinical entity and most of those who are aware ...
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...
Abstract DNA from a human-hamster hybrid cell line, 908-K1B17, containing a small terminal port...
The q26-q28 region of the human X chromosome contains several important disease loci, including the ...
The X chromosome is probably the most studied of all human chromosomes, in part because more than 11...
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...
The Fragile X Syndrome is the most common cause of heritable mental retardation, affecting one in 20...
Conclusion Rapid progress has been made in the analysis of the fragile X syndrome during 1991. Di...
A panel of somatic cell hybrids and X-linked hypohidrotic ectodermal dysplasia (EDA) patient-derived...
The human gene for glucose-6-phosphate dehydrogenase (G6PD) has been subregionally mapped to band Xq...
A panel of somatic cell hybrids and X-linked hypohidrotic ectodermal dysplasia (EDA) patient-derived...
The human gene for glucose-6-phosphate dehydrogenase (G6PD) has been subregionally mapped to band Xq...
Fragile X syndrome is now a well established common clinical entity and most of those who are aware ...