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STAG1 mutations cause a novel cohesinopathy characterised by unspecific syndromic intellectual disability
- Authors :
- Genetica Klinische Genetica
Child Health
Genetica Sectie Genoomdiagnostiek
Lehalle, Daphné
Mosca-Boidron, Anne-Laure
Begtrup, Amber
Boute-Benejean, Odile
Charles, Perrine
Cho, Megan T
Clarkson, Amanda
Devinsky, Orrin
Duffourd, Yannis
Duplomb-Jego, Laurence
Gérard, Bénédicte
Jacquette, Aurélia
Kuentz, Paul
Masurel-Paulet, Alice
McDougall, Carey
Moutton, Sébastien
Olivié, Hilde
Park, Soo-Mi
Rauch, Anita
Revencu, Nicole
Rivière, Jean-Baptiste
Rubin, Karol
Simonic, Ingrid
Shears, Deborah J
Smol, Thomas
Taylor Tavares, Ana Lisa
Terhal, Paulien
Thevenon, Julien
Van Gassen, Koen
Vincent-Delorme, Catherine
Willemsen, Marjolein H
Wilson, Golder N
Zackai, Elaine
Zweier, Christiane
Callier, Patrick
Thauvin-Robinet, Christel
Faivre, Laurence
Genetica Klinische Genetica
Child Health
Genetica Sectie Genoomdiagnostiek
Lehalle, Daphné
Mosca-Boidron, Anne-Laure
Begtrup, Amber
Boute-Benejean, Odile
Charles, Perrine
Cho, Megan T
Clarkson, Amanda
Devinsky, Orrin
Duffourd, Yannis
Duplomb-Jego, Laurence
Gérard, Bénédicte
Jacquette, Aurélia
Kuentz, Paul
Masurel-Paulet, Alice
McDougall, Carey
Moutton, Sébastien
Olivié, Hilde
Park, Soo-Mi
Rauch, Anita
Revencu, Nicole
Rivière, Jean-Baptiste
Rubin, Karol
Simonic, Ingrid
Shears, Deborah J
Smol, Thomas
Taylor Tavares, Ana Lisa
Terhal, Paulien
Thevenon, Julien
Van Gassen, Koen
Vincent-Delorme, Catherine
Willemsen, Marjolein H
Wilson, Golder N
Zackai, Elaine
Zweier, Christiane
Callier, Patrick
Thauvin-Robinet, Christel
Faivre, Laurence
- Publication Year :
- 2017
Details
- Database :
- OAIster
- Notes :
- English
- Publication Type :
- Electronic Resource
- Accession number :
- edsoai.on1395293526
- Document Type :
- Electronic Resource