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MAGEL2 gene

Known as: nM15, NDNL1, MAGEL2 
 
National Institutes of Health

Papers overview

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Review
2016
Review
2016
Prader-Willi syndrome (PWS) is a neurodevelopmental disorder characterized by neonatal hypotonia, developmental delay… Expand
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2015
2015
Arthrogryposis multiplex congenita (AMC) is characterized by the presence of multiple joint contractures resulting from reduced… Expand
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Highly Cited
2015
Highly Cited
2015
BACKGROUND Mutations of MAGEL2 have been reported in patients presenting with autism, and loss of MAGEL2 is also associated with… Expand
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2011
2011
Hypothalamic dysfunction may underlie endocrine abnormalities in Prader-Willi syndrome (PWS), a genetic disorder that features GH… Expand
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Highly Cited
2010
Highly Cited
2010
The onset of feeding at birth is a vital step for the adaptation of the neonate to extra uterine life. Prader-Willi syndrome (PWS… Expand
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Highly Cited
2009
Highly Cited
2009
The Prader–Willi syndrome (PWS) is caused by a 5–6 Mbp de novo deletion on the paternal chromosome 15, maternal uniparental… Expand
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2009
2009
BACKGROUND MAGEL2 is one of several genes typically inactivated in the developmental obesity disorder Prader-Willi syndrome (PWS… Expand
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Highly Cited
2000
Highly Cited
2000
Prader-Willi syndrome (PWS) is a neurogenetic disease characterized by infantile hypotonia, gonadal hypoplasia, obsessive… Expand
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Highly Cited
2000
Highly Cited
2000
Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13. Affected individuals… Expand
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Highly Cited
1999
Highly Cited
1999
Prader-Willi syndrome (PWS) is a complex neurogenetic disorder. The phenotype is likely to be a contiguous gene syndrome… Expand
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