Candice Feben

Johannesburg, GT, South Africa

Last Updated: 09/26/2026

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Found 11 publications

Case Report: FBN1 mutation screening in South African patients with Marfan syndrome.

Case Report: FBN1 mutation screening in South African patients with Marfan syndrome.

Journal: Frontiers in genetics

Published: April 15, 2025

Mutation analysis and clinical profile of South African patients with Neurofibromatosis type 1 (NF1) phenotype.

Mutation analysis and clinical profile of South African patients with Neurofibromatosis type 1 (NF1) phenotype.

Journal: Frontiers in genetics

Published: October 31, 2023

Mutation profiling in South African patients with Cornelia de Lange syndrome phenotype.

Mutation profiling in South African patients with Cornelia de Lange syndrome phenotype.

Journal: Molecular genetics & genomic medicine

Published: September 07, 2023

A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments.

A feasible molecular diagnostic strategy for rare genetic disorders within resource-constrained environments.

Journal: Journal of community genetics

Published: February 03, 2023

Ending a diagnostic odyssey-The first case of Takenouchi-Kosaki syndrome in an African patient.

Ending a diagnostic odyssey-The first case of Takenouchi-Kosaki syndrome in an African patient.

Journal: Clinical case reports

Published: December 22, 2020

Two novel presentations of KCNMA1-related pathology--Expanding the clinical phenotype of a rare channelopathy.

Two novel presentations of KCNMA1-related pathology--Expanding the clinical phenotype of a rare channelopathy.

Journal: Molecular genetics & genomic medicine

Published: November 24, 2020

Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation.

Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation.

Journal: Molecular genetics & genomic medicine

Published: February 21, 2020

Fanconi anaemia in South Africa: Past, present and future.

Fanconi anaemia in South Africa: Past, present and future.

Journal: South African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde

Published: April 25, 2018

Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.

Biallelic BRCA2 mutations in two black South African children with Fanconi anaemia.

Journal: Familial cancer

Published: February 11, 2017

Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia.

Hematological consequences of a FANCG founder mutation in Black South African patients with Fanconi anemia.

Journal: Blood cells, molecules & diseases

Published: October 22, 2014

Phenotypic consequences in black South African Fanconi anemia patients homozygous for a founder mutation.

Phenotypic consequences in black South African Fanconi anemia patients homozygous for a founder mutation.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: March 15, 2013

Showing 1-11 of 11

Last Updated: 09/26/2026