Publications by authors named "Candice Feben"

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Mutation analysis and clinical profile of South African patients with Neurofibromatosis type 1 (NF1) phenotype.
Maria Mabyalwa Mudau, Bronwyn Dillon, Clarice Smal, Candice Feben, Engela Honey

Front Genet· March 2024

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A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments.
Maria Mabyalwa Mudau, Heather Seymour, Patracia Nevondwe, Robyn Kerr, Careni Spencer, Candice Feben

J Community Genet· February 2024

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Mutation profiling in South African patients with Cornelia de Lange syndrome phenotype.
Heather Seymour, Candice Feben, Patracia Nevondwe, Robyn Kerr, Careni Spencer

Mol Genet Genomic Med· January 2024

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Two novel presentations of KCNMA1-related pathology--Expanding the clinical phenotype of a rare channelopathy.
Jotte Rodrigues Bento, Candice Feben, Marlies Kempers, Maartje van Rij, Mallory Woiski

Mol Genet Genomic Med· October 2021

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Ending a diagnostic odyssey-The first case of Takenouchi-Kosaki syndrome in an African patient.
Kaitlyn Flynn, Candice Feben, Lindiwe Lamola, Nadia Carstens, Amanda Krause

Clin Case Rep· April 2021

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Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation.
Bronwyn Dillon, Candice Feben, David Segal, Johannes du Plessis, David Reynders

Mol Genet Genomic Med· August 2020

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Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.
Candice Feben, Careni Spencer, Anneline Lochan, Nakita Laing, Karen Fieggen

Fam Cancer· July 2017

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Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia.
Candice Feben, Jennifer Kromberg, Rosalind Wainwright, David Stones, Janet Poole

Blood Cells Mol Dis· March 2015

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Phenotypic consequences in black South African Fanconi anemia patients homozygous for a founder mutation.
Candice Feben, Jennifer Kromberg, Rosalind Wainwright, David Stones, Chris Sutton

Genet Med· May 2014

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