: A multilocus analysis of the fragile X (fra(X] syndrome was conducted with 147 families. Two proximal loci, DXS51 and F9, and two distal loci, DXS52 and DXS15, were studied. Overall, the best multipoint distances were found to be DXS51-F9, 6.9%, F9-fra(X), 22.4%; fra(X)-DXS52, 12.7%; DXS52-DXS15, 2.2%. These distances can be used for multipoint mapping of new probes, carrier testing and counseling of fra(X) families. Consistent with several previous studies, the families as a whole showed genetic heterogeneity for linkage between F9 and fra(X)
Several studies have suggested that fragileXsyndrome (FRAXA), the most common inherited form of ment...
The X chromosome is probably the most studied of all human chromosomes, in part because more than 11...
Several studies have suggested that fragileXsyndrome (FRAXA), the most common inherited form of ment...
: A multilocus analysis of the fragile X (fra(X] syndrome was conducted with 147 families. Two proxi...
: A multilocus analysis of the fragile X (fra(X] syndrome was conducted with 147 families. Two proxi...
The X-linked fragile X [fra(X)] syndrome, associated with a fragile site at Xq27.3, is the most comm...
The q26-q28 region of the human X chromosome contains several important disease loci, including the ...
Previously, we showed genetic heterogeneity for linkage between the fra(X) locus and a factor IX DNA...
Direct diagnosis by DNA analysis of the fragile X syndrome was studied in 511 persons from 63 famili...
Genetic linkage between a factor IX DNA restriction fragment length polymorphism (RFLP) and the frag...
The discovery of the Fragile X (fra(X] syndrome represents a major advance in our understanding of m...
Of the seven folate-sensitive fragile sites cloned in the human genome, only two have a proven clini...
al probe that identifies a highly informative two-allele TaqI restriction fragment length polymorphi...
Fragile X syndrome is an X-linked dominant disorder with incomplete penetrance that is a common caus...
Several studies have suggested that fragileXsyndrome (FRAXA), the most common inherited form of ment...
Several studies have suggested that fragileXsyndrome (FRAXA), the most common inherited form of ment...
The X chromosome is probably the most studied of all human chromosomes, in part because more than 11...
Several studies have suggested that fragileXsyndrome (FRAXA), the most common inherited form of ment...
: A multilocus analysis of the fragile X (fra(X] syndrome was conducted with 147 families. Two proxi...
: A multilocus analysis of the fragile X (fra(X] syndrome was conducted with 147 families. Two proxi...
The X-linked fragile X [fra(X)] syndrome, associated with a fragile site at Xq27.3, is the most comm...
The q26-q28 region of the human X chromosome contains several important disease loci, including the ...
Previously, we showed genetic heterogeneity for linkage between the fra(X) locus and a factor IX DNA...
Direct diagnosis by DNA analysis of the fragile X syndrome was studied in 511 persons from 63 famili...
Genetic linkage between a factor IX DNA restriction fragment length polymorphism (RFLP) and the frag...
The discovery of the Fragile X (fra(X] syndrome represents a major advance in our understanding of m...
Of the seven folate-sensitive fragile sites cloned in the human genome, only two have a proven clini...
al probe that identifies a highly informative two-allele TaqI restriction fragment length polymorphi...
Fragile X syndrome is an X-linked dominant disorder with incomplete penetrance that is a common caus...
Several studies have suggested that fragileXsyndrome (FRAXA), the most common inherited form of ment...
Several studies have suggested that fragileXsyndrome (FRAXA), the most common inherited form of ment...
The X chromosome is probably the most studied of all human chromosomes, in part because more than 11...
Several studies have suggested that fragileXsyndrome (FRAXA), the most common inherited form of ment...