AbstractMolecular analysis of a small hemizygous deletion in a patient with partial Williams syndrome suggests that loss of the LIM-Kinase 1 gene may be responsible for the impaired visuospatial constructive cognition characteristic of the syndrome
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
AbstractA unique opportunity to understand genetic determinants of cognition is offered by Williams ...
AbstractTo identify genes important for human cognitive development, we studied Williams syndrome (W...
AbstractTo identify genes important for human cognitive development, we studied Williams syndrome (W...
SummaryIn Williams syndrome (WS), a deletion of ∼1.5 Mb on one copy of chromosome 7 causes specific ...
SummaryIn Williams syndrome (WS), a deletion of ∼1.5 Mb on one copy of chromosome 7 causes specific ...
Williams syndrome (WS) is a multisystem developmental disorder caused by the deletion of contiguous ...
Background\ud \ud Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizy...
BACKGROUND: Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic ...
BACKGROUND: Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic ...
Background Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic ...
Williams Syndome (WS) is as complex neurodevelopmental disorder characterized by vascular and heart ...
Abstract Background Williams syndrome (WS), a rare neurodevelopmental disorder caused by hemizygous ...
Williams syndrome (WS) is a genetic disorder associated with impairments of spatial cognition. This ...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
AbstractA unique opportunity to understand genetic determinants of cognition is offered by Williams ...
AbstractTo identify genes important for human cognitive development, we studied Williams syndrome (W...
AbstractTo identify genes important for human cognitive development, we studied Williams syndrome (W...
SummaryIn Williams syndrome (WS), a deletion of ∼1.5 Mb on one copy of chromosome 7 causes specific ...
SummaryIn Williams syndrome (WS), a deletion of ∼1.5 Mb on one copy of chromosome 7 causes specific ...
Williams syndrome (WS) is a multisystem developmental disorder caused by the deletion of contiguous ...
Background\ud \ud Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizy...
BACKGROUND: Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic ...
BACKGROUND: Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic ...
Background Williams syndrome (WS) is a rare neurodevelopmental disorder arising from a hemizygotic ...
Williams Syndome (WS) is as complex neurodevelopmental disorder characterized by vascular and heart ...
Abstract Background Williams syndrome (WS), a rare neurodevelopmental disorder caused by hemizygous ...
Williams syndrome (WS) is a genetic disorder associated with impairments of spatial cognition. This ...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
Williams syndrome (WS) is a contiguous gene syndrome caused by hemizygous deletion of approximately ...
AbstractA unique opportunity to understand genetic determinants of cognition is offered by Williams ...
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