Publications by authors named "Stephen Tennant"

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PACS2, PACS1, and VACTERL: A Clinical Overlap.
Hannah Massey, Stephen Tennant, John Dean,

Mol Syndromol· February 2025

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A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorder.
François Lecoquierre, A Mattijs Punt, Frédéric Ebstein, Ilse Wallaard, Rob Verhagen, Stephen Tennant

Genet Med· June 2024

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Long QT syndrome and left ventricular noncompaction in 4 family members across 2 generations with KCNQ1 mutation.
Mira Kharbanda, Amanda Hunter, Stephen Tennant, David Moore, Stephanie Curtis

Eur J Med Genet· May 2017

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Genetics in reverse.
Patrick F Chinnery, Niall E F Cartlidge, Stephen Tennant, Daniel Birchall, Su A R Stenhouse

Lancet· January 2004

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