Publications by authors named "Liani Smit"

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STAC3 disorder: a common cause of congenital hypotonia in Southern African patients.
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Liani Smit

Eur J Hum Genet· January 2025

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Correction: STAC3 disorder: a common cause of congenital hypotonia in Southern African patients.
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Liani Smit

Eur J Hum Genet· July 2024

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Utility of genetic testing in children with developmental and epileptic encephalopathy (DEE) at a tertiary hospital in South Africa: A prospective study.
Farida Essajee, Michael Urban, Liani Smit, Jo M Wilmshurst, Regan Solomons

Seizure· October 2022

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Hyperphosphatasia with mental retardation syndrome type 4 in three unrelated South African patients.
Heidre Bezuidenhout, Samantha Bayley, Liani Smit, Craig Kinnear, Marlo Möller

Am J Med Genet A· October 2020

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CHARGE syndrome: genetic aspects and dental challenges, a review and case presentation.
Manogari Chetty, Tina Sharon Roberts, Mona Elmubarak, Heidre Bezuidenhout, Liani Smit

Head Face Med· May 2020

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A Community Perspective on the Inclusion of Pregnant Women in Tuberculosis Drug Trials.
Lindsay McKenna, Mike Frick, Cynthia Lee, Dorothy Namutamba, Liani Smit

Clin Infect Dis· October 2017

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