6q16.3q23.3 duplication associated with Prader-Willi-like syndrome.

Laurent Desch,Nathalie Marle,Anne-Laure Mosca-Boidron,Laurence Faivre,Marie Eliade,Muriel Payet,Clémence Ragon,Julien Thevenon,Bernard Aral,Sylviane Ragot,Azarnouche Ardalan,Nabila Dhouibi,Candace Bensignor,Christel Thauvin-Robinet,Salima El Chehadeh,Patrick Callier

6q16.3q23.3 duplication associated with Prader-Willi-like syndrome.

2015

Laurent Desch
Nathalie Marle
Anne-Laure Mosca-Boidron
Laurence Faivre
Marie Eliade
Muriel Payet
Clémence Ragon
Julien Thevenon
Bernard Aral
Sylviane Ragot
Azarnouche Ardalan
Nabila Dhouibi
Candace Bensignor
Christel Thauvin-Robinet
Salima El Chehadeh
Patrick Callier

Background Prader-Willi syndrome (PWS) is characterized by hypotonia, delayed neuropsychomotor development, overeating, obesity and mental deficiency. This phenotype is encountered in other conditions, defining Prader-Willi-like syndrome (PWLS).

Keywords:

Obesity
Hypotonia
Bioinformatics
Phenotype
Overeating
PRADER-WILLI-LIKE SYNDROME
Cytogenetics
Gene duplication
Biology
Human genetics

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