Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling (Q29147391)
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Language | Label | Description | Also known as |
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English | Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling |
scientific journal article |
Statements
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Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling (English)
1 reference
Eric Smeets
2 references
Han Brunner
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Evan E Eichler
Usha Kini
2 references
Ruth Newbury-Ecob
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Eric Haan
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Marie Shaw
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Melanie Bienek
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Corinna Jensen
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Bregje W M van Bon
Hilde Van Esch
Kees van Roozendaal
2 references
Nicholas Katsanis
2 references
Tjitske Kleefstra
Andreas Rump
2 references
Rolph Pfundt
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A Micheil Innes
Jolanda Schieving
2 references
Jane Juusola
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Margot R F Reijnders
Janneke Schuurs-Hoeijmakers
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Christian Gilissen
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Alexander Hoischen
Erik Madsen
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Willemijn Wissink-Lindhout
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Connie Stumpel
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Maaike Vreeburg
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Karin Oberndorff
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Hilary Racher
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Katrina Tatton-Brown
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Alex Henderson
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Alan Fryer
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Alison Ross
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Pradeep Vasudevan
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Kate Chandler
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Alison Male
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DDD Study
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Sybe Dijkstra
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Jacques Giltay
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Igor Pediaditakis
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Kyle Retterer
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Patrick Reed
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Eden Haverfield
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Marvin Natowicz
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Angela Myers
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Katherine Keating
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Joel Charrow
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Jennifer Norman
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Audrey Foster-Barber
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Amy Kimball
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Margaret Harr
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Joyce Fox
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Julie McLaughlin
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Kristin Lindstrom
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Megan T Cho
Tom S Koemans
Sascha Vermeer
Michael J Parker
Sally A Lynch
Perciliz L Tan
Kristin G Monaghan
Michael C Kruer
Kevin A Strauss
Karlla W Brigatti
Barbara K Burton
Katherine H Kim
Antonie D Kline
Elaine Zackai
Katrina M Haude
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