Prader-Willi syndrome (PWS) is a congenital developmental disorder of childhood, characterized by mental retardation, neonatal hypotonia and feeding difficulty followed by excessive eating in childhood which leads to obesity. It is caused by an absence of 15q11-13 region on a paternally derived chromosome 15. This is an imprinted region which contains several imprinted genes. The majority of PWS cases are caused by an interstitial deletion of the PWS critical region. Some are cause
Prader-Willi syndrome (PWS) is a congenital neurodevelopmental disorder caused by loss of function o...
Prader-Willi syndrome (PWS) is a developmental disorder caused by a deficiency of paternal contribut...
Thirty-seven patients presenting features of the Prader-Willi syndrome (PWS) have been examined usin...
Prader–Willi syndrome (PWS) is a contiguous gene syndrome caused by the loss of function of genes si...
Prader-Willi syndrome (PWS) is characterised by infantilehypotonia, feeding difficulties, hypogonadi...
BACKGROUND. Prader—Willi syndrome is a genetic disorder characterized by infantile hypotonia, obesit...
BackgroundPrader-Willi syndrome (PWS) is due to errors in genomic imprinting. PWS is recognised as t...
Prader-Willi syndrome (PWS) is caused by a deficiency of imprinted genes in the 15q11-q13 region and...
Abstract We describe two Prader-Willi syndrome (PWS) patients who exhibit maternal uniparental disom...
Abstract Background Prader-Willi syndrome (PWS) is a multisystemic complex genetic disorder caused b...
BackgroundPrader-Willi syndrome (PWS) is due to errors in genomic imprinting. PWS is recognised as t...
Prader-Willi syndrome (PWS) is a complex, multisystem genetic disorder characterized by endocrine, n...
Background: Prader-Willi syndrome (PWS) is a rare genetic disorder resulting from the lack of expres...
BackgroundPrader-Willi syndrome (PWS) is an imprinting disorder caused by the absence of paternal ex...
Here we describe the genetic studies performed in 53 patients with the suspected diagnosis of Prader...
Prader-Willi syndrome (PWS) is a congenital neurodevelopmental disorder caused by loss of function o...
Prader-Willi syndrome (PWS) is a developmental disorder caused by a deficiency of paternal contribut...
Thirty-seven patients presenting features of the Prader-Willi syndrome (PWS) have been examined usin...
Prader–Willi syndrome (PWS) is a contiguous gene syndrome caused by the loss of function of genes si...
Prader-Willi syndrome (PWS) is characterised by infantilehypotonia, feeding difficulties, hypogonadi...
BACKGROUND. Prader—Willi syndrome is a genetic disorder characterized by infantile hypotonia, obesit...
BackgroundPrader-Willi syndrome (PWS) is due to errors in genomic imprinting. PWS is recognised as t...
Prader-Willi syndrome (PWS) is caused by a deficiency of imprinted genes in the 15q11-q13 region and...
Abstract We describe two Prader-Willi syndrome (PWS) patients who exhibit maternal uniparental disom...
Abstract Background Prader-Willi syndrome (PWS) is a multisystemic complex genetic disorder caused b...
BackgroundPrader-Willi syndrome (PWS) is due to errors in genomic imprinting. PWS is recognised as t...
Prader-Willi syndrome (PWS) is a complex, multisystem genetic disorder characterized by endocrine, n...
Background: Prader-Willi syndrome (PWS) is a rare genetic disorder resulting from the lack of expres...
BackgroundPrader-Willi syndrome (PWS) is an imprinting disorder caused by the absence of paternal ex...
Here we describe the genetic studies performed in 53 patients with the suspected diagnosis of Prader...
Prader-Willi syndrome (PWS) is a congenital neurodevelopmental disorder caused by loss of function o...
Prader-Willi syndrome (PWS) is a developmental disorder caused by a deficiency of paternal contribut...
Thirty-seven patients presenting features of the Prader-Willi syndrome (PWS) have been examined usin...