Genetic analysis in a boy aged 8 years 10 months with severe delay in expressive language and orofacial dyspraxia uncovered reciprocal duplications of the Williams-Beuren syndrome (WBS) locus at chromosome 7q11.23, in a report from the University of Alberta, and other centers in Canada, USA, and Spain
Williams–Beuren syndrome (WBS) is a common microdeletion syndrome characterized by a 1.5Mb deletion ...
Williams-Beuren syndrome is a rare genetic disorder with prevalence 1:10.000. Microdeletion on chrom...
Williams or Williams -Beuren Syndrome (WS) is a very rare syndrome associated with a microdeletion o...
We report on a new duplication case of 7q11.23, reciprocal of the Williams-Beuren (WB) deletion. The...
Interstitial deletions of 7q11.23 cause Williams-Beuren syndrome, one of the best characterized micr...
unequal recombination between repeated sequences, are found in a subset of patients with autism. Dup...
Background: Deletion of the Williams-Beuren syndrome (WBS) critical region (WBSCR), at 7q11.23, caus...
Williams-Beuren Syndrome (WBS) is a rare, most often sporadic, genetic disease caused by a chromosom...
International audienceBACKGROUND: Chromosomal rearrangements, arising from unequal recombination bet...
Whether genetic or environmental influences predominate in defining thought, behavior, and physical ...
Genomic rearrangements, particularly deletions and duplications, are known to cause many genetic dis...
Williams-Beuren syndrome (WBS) is a rare neurodevelopmental disorder characterized by a set of somat...
Williams-Beuren syndrome (WBS) is a rare neurodevelopmental disorder characterized by a set of somat...
International audienceBACKGROUND: Deletion of the Williams-Beuren syndrome (WBS) critical region (WB...
Williams-Beuren region reciprocal duplication A significant recent finding in neurogenetics is the c...
Williams–Beuren syndrome (WBS) is a common microdeletion syndrome characterized by a 1.5Mb deletion ...
Williams-Beuren syndrome is a rare genetic disorder with prevalence 1:10.000. Microdeletion on chrom...
Williams or Williams -Beuren Syndrome (WS) is a very rare syndrome associated with a microdeletion o...
We report on a new duplication case of 7q11.23, reciprocal of the Williams-Beuren (WB) deletion. The...
Interstitial deletions of 7q11.23 cause Williams-Beuren syndrome, one of the best characterized micr...
unequal recombination between repeated sequences, are found in a subset of patients with autism. Dup...
Background: Deletion of the Williams-Beuren syndrome (WBS) critical region (WBSCR), at 7q11.23, caus...
Williams-Beuren Syndrome (WBS) is a rare, most often sporadic, genetic disease caused by a chromosom...
International audienceBACKGROUND: Chromosomal rearrangements, arising from unequal recombination bet...
Whether genetic or environmental influences predominate in defining thought, behavior, and physical ...
Genomic rearrangements, particularly deletions and duplications, are known to cause many genetic dis...
Williams-Beuren syndrome (WBS) is a rare neurodevelopmental disorder characterized by a set of somat...
Williams-Beuren syndrome (WBS) is a rare neurodevelopmental disorder characterized by a set of somat...
International audienceBACKGROUND: Deletion of the Williams-Beuren syndrome (WBS) critical region (WB...
Williams-Beuren region reciprocal duplication A significant recent finding in neurogenetics is the c...
Williams–Beuren syndrome (WBS) is a common microdeletion syndrome characterized by a 1.5Mb deletion ...
Williams-Beuren syndrome is a rare genetic disorder with prevalence 1:10.000. Microdeletion on chrom...
Williams or Williams -Beuren Syndrome (WS) is a very rare syndrome associated with a microdeletion o...
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