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Paper Details

Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder.
Hum Mol Genet
46
2018
Author NameAffiliation
Kelly Schoch
Xi LuoBaylor College of Medicine
Loren D M Pena
Zöe PowisClinical Genomics
Kelly RadtkeClinical Genomics
Allyn McConkie-Rosell
Anna C NeedImperial College London
David BickHudsonAlpha Institute for Biotechnology
David BickHudsonAlpha Institute for Biotechnology
Elizabeth A WortheyHudsonAlpha Institute for Biotechnology
Elizabeth A WortheyHudsonAlpha Institute for Biotechnology
Shawn LevyHudsonAlpha Institute for Biotechnology
Shawn LevyHudsonAlpha Institute for Biotechnology
Michael F WanglerBaylor College of Medicine
Michael F WanglerJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital
Michael F WanglerBaylor College of Medicine
Hugo J BellenBaylor College of Medicine
Hugo J BellenHoward Hughes Medical Institute
Hugo J BellenBaylor College of Medicine
Hugo J BellenBaylor College of Medicine
Hugo J BellenJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital
Hugo J BellenBaylor College of Medicine
Hugo J BellenJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital
Hugo J BellenBaylor College of Medicine
Hugo J BellenBaylor College of Medicine
Hugo J BellenHoward Hughes Medical Institute
Vandana Shashi
Shinya YamamotoBaylor College of Medicine
Shinya YamamotoJan and Dan Duncan Neurological Research Institute, Texas Children's Hospital
Shinya YamamotoBaylor College of Medicine
Shinya YamamotoBaylor College of Medicine
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