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Hearing loss in Africa: current genetic profile.
Adadey SM, Wonkam-Tingang E, Aboagye ET, Quaye O, Awandare GA, Wonkam A. Adadey SM, et al. Among authors: wonkam a, wonkam tingang e. Hum Genet. 2022 Apr;141(3-4):505-517. doi: 10.1007/s00439-021-02376-y. Epub 2021 Oct 5. Hum Genet. 2022. PMID: 34609590 Free PMC article. Review.
Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian families.
Lebeko K, Sloan-Heggen CM, Noubiap JJ, Dandara C, Kolbe DL, Ephraim SS, Booth KT, Azaiez H, Santos-Cortez RL, Leal SM, Smith RJ, Wonkam A. Lebeko K, et al. Among authors: wonkam a. Clin Genet. 2016 Sep;90(3):288-90. doi: 10.1111/cge.12799. Epub 2016 Jun 1. Clin Genet. 2016. PMID: 27246798 Free PMC article.
Noonan Syndrome in South Africa: Clinical and Molecular Profiles.
Tekendo-Ngongang C, Agenbag G, Bope CD, Esterhuizen AI, Wonkam A. Tekendo-Ngongang C, et al. Among authors: wonkam a. Front Genet. 2019 Apr 16;10:333. doi: 10.3389/fgene.2019.00333. eCollection 2019. Front Genet. 2019. PMID: 31057598 Free PMC article.
230 results