Turner syndrome (TS) is associated with a characteristic neurocognitive profile that includes impaired visuospatial/perceptual abilities. We used a molecular approach to identify a critical region of the X chromosome for neurocognitive aspects of TS. Partial deletions of Xp in 34 females were mapped by FISH or by loss of heterozygosity of polymorphic markers. Discriminant function analysis optimally identified the TS-associated neurocognitive phenotype. Only subjects missing ∼10 Mb of distal Xp manifested the specified neurocognitive profile. The phenotype was seen with either paternally or maternally inherited deletions and with either complete or incomplete skewing of X inactivation. Fine mapping of informative deletions implicated a crit...
Turner syndrome (TS) is a chromosomal condition associated with partial or complete absence of the X...
Turner syndrome (TS) is a genetic disorder seen in phenotypically female (pf) individuals who have e...
Girls and women with Turner syndrome (TS) have a completely or partially missing X chromosome. Exten...
Turner syndrome (TS) is associated with a characteristic neurocognitive profile that includes impair...
BACKGROUND: Turner syndrome (TS) is associated with a neurocognitive phenotype that includes selecti...
Turner Syndrome (TS) is a genetic condition characterized by the partial or complete loss of one se...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Piagetian scales and the Bender ...
X-monosomy is a form of Turner syndrome (TS) in which an entire X chromosome is missing. It is usual...
Turner's syndrome is a sporadic disorder of human females in which all or part of one X chromosome i...
Women with Turner's syndrome (TS) allow us to study the neurobiological associates of cognitive and ...
Turner syndrome is a genetic disorder that results from an abnormal or missing X chromosome in femal...
We report a detailed phenotypic, cytogenetic and molecular characterization of a patient prenatally ...
Women with Turner's syndrome (TS) allow us to study the neurobiological associates of cognitive and ...
†These authors contributed equally to this work. Turner syndrome (TS), a disorder caused by the cong...
The absence of all or part of one X chromosome in female humans causes Turner’s syndrome (TS), provi...
Turner syndrome (TS) is a chromosomal condition associated with partial or complete absence of the X...
Turner syndrome (TS) is a genetic disorder seen in phenotypically female (pf) individuals who have e...
Girls and women with Turner syndrome (TS) have a completely or partially missing X chromosome. Exten...
Turner syndrome (TS) is associated with a characteristic neurocognitive profile that includes impair...
BACKGROUND: Turner syndrome (TS) is associated with a neurocognitive phenotype that includes selecti...
Turner Syndrome (TS) is a genetic condition characterized by the partial or complete loss of one se...
Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Piagetian scales and the Bender ...
X-monosomy is a form of Turner syndrome (TS) in which an entire X chromosome is missing. It is usual...
Turner's syndrome is a sporadic disorder of human females in which all or part of one X chromosome i...
Women with Turner's syndrome (TS) allow us to study the neurobiological associates of cognitive and ...
Turner syndrome is a genetic disorder that results from an abnormal or missing X chromosome in femal...
We report a detailed phenotypic, cytogenetic and molecular characterization of a patient prenatally ...
Women with Turner's syndrome (TS) allow us to study the neurobiological associates of cognitive and ...
†These authors contributed equally to this work. Turner syndrome (TS), a disorder caused by the cong...
The absence of all or part of one X chromosome in female humans causes Turner’s syndrome (TS), provi...
Turner syndrome (TS) is a chromosomal condition associated with partial or complete absence of the X...
Turner syndrome (TS) is a genetic disorder seen in phenotypically female (pf) individuals who have e...
Girls and women with Turner syndrome (TS) have a completely or partially missing X chromosome. Exten...