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Stephen Tennant

Showing results (1-10 of 4) with videos related to

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Molecular Syndromology|February 6, 2025
PACS2, PACS1, and VACTERL: A Clinical OverlapHannah Massey, Stephen Tennant, John Dean, et al.
Lancet (London, England)|January 31, 2004
Genetics in reversePatrick F Chinnery, Niall E F Cartlidge, Stephen Tennant, et al.
European Journal of Medical Genetics|March 3, 2017
Long QT syndrome and left ventricular noncompaction in 4 family members across 2 generations with KCNQ1 mutationMira Kharbanda, Amanda Hunter, Stephen Tennant, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 11, 2024
A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorderFrançois Lecoquierre, A Mattijs Punt, Frédéric Ebstein, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Molecular Syndromology|February 6, 2025
PACS2, PACS1, and VACTERL: A Clinical OverlapHannah Massey, Stephen Tennant, John Dean, et al.
Lancet (London, England)|January 31, 2004
Genetics in reversePatrick F Chinnery, Niall E F Cartlidge, Stephen Tennant, et al.
European Journal of Medical Genetics|March 3, 2017
Long QT syndrome and left ventricular noncompaction in 4 family members across 2 generations with KCNQ1 mutationMira Kharbanda, Amanda Hunter, Stephen Tennant, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 11, 2024
A recurrent missense variant in the E3 ubiquitin ligase substrate recognition subunit FEM1B causes a rare syndromic neurodevelopmental disorderFrançois Lecoquierre, A Mattijs Punt, Frédéric Ebstein, et al.
Pageof 1