Christopher T Gordon
20PUBLICATIONS
68CO-AUTHORS
Get your video featured.
Publish with JoVEGet your video featured.
Publish with JoVE
Publications (20)
Sort by Publication Date:
|Mar 11, 2024
The spectrum of heart defects in the <i>TRAF7</i>-related multiple congenital anomalies-intellectual disability syndrome.Elise Pisan, Chiara De Luca, Francesco Brancati
|Feb 22, 2024
TREX tetramer disruption alters RNA processing necessary for corticogenesis in THOC6 Intellectual Disability Syndrome.Elizabeth A Werren, Geneva R LaForce, Anshika Srivastava
|Sep 18, 2023
Mechanisms of mRNA processing defects in inherited <i>THOC6</i> intellectual disability syndrome.Elizabeth Werren, Geneva LaForce, Anshika Srivastava
|Sep 04, 2023
Biallelic truncating variants in <i>VGLL2</i> cause syngnathia in humans.Valeria Agostini, Aude Tessier, Nabila Djaziri
|Jul 27, 2023
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delays.Mythily Ganapathi, Leticia S Matsuoka, Michael March
|Apr 09, 2022
Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humans.Anne Guimier, Loïc de Pontual, Stephen R Braddock
Pageof 4
Frequent Collaborators
3 joint publications
Bruno Reversade
3 joint publications
Tania Attié-Bitach
2 joint publications
Emmanuelle Szenker-Ravi
2 joint publications
Katta M Girisha
2 joint publications
Stephanie L Bielas
2 joint publications
Ashleigh Schaffer
2 joint publications
Vydianathan Ravi
2 joint publications
Guillaume Louvel
2 joint publications
Anja Beckers
2 joint publications
William G Newman
