Publications by authors named "Cedrik Tekendo-Ngongang"

13Publications

Noonan syndrome on the African Continent.

Birth Defects Res 2020 Jun;112(10):718-724

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/bdr2.1675DOI Listing
June 2020

MECP2 duplication syndrome in a patient from Cameroon.

Am J Med Genet A 2020 04 13;182(4):619-622. Epub 2020 Feb 13.

Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.a.61510DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7450984PMC
April 2020

Comorbidity of congenital heart defects and holoprosencephaly is likely genetically driven and gene-specific.

Am J Med Genet C Semin Med Genet 2020 03 5;184(1):154-158. Epub 2020 Feb 5.

Medical Genetics Branch, National Human Genome Research Institutes, National Institutes of Health, Bethesda, Maryland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1002/ajmg.c.31770DOI Listing
March 2020

Diversity and dysmorphology.

Curr Opin Pediatr 2019 12;31(6):702-707

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1097/MOP.0000000000000816DOI Listing
December 2019

Novel heterozygous variants in KMT2D associated with holoprosencephaly.

Clin Genet 2019 09 15;96(3):266-270. Epub 2019 Jul 15.

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1111/cge.13598DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6690755PMC
September 2019

Noonan Syndrome in South Africa: Clinical and Molecular Profiles.

Front Genet 2019 16;10:333. Epub 2019 Apr 16.

Division of Human Genetics, Departments of Medicine and Pathology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

View Article

Download full-text PDF

Source
https://www.frontiersin.org/article/10.3389/fgene.2019.00333
Publisher Site
http://dx.doi.org/10.3389/fgene.2019.00333DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6477999PMC
April 2019

Williams-Beuren syndrome in diverse populations.

Am J Med Genet A 2018 05;176(5):1128-1136

Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/ajmg.a.38672
Publisher Site
http://dx.doi.org/10.1002/ajmg.a.38672DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007881PMC
May 2018

The 22q11.2 Deletion Syndrome in Congenital Heart Defects: Prevalence of Microdeletion Syndrome in Cameroon.

Glob Heart 2017 06 13;12(2):115-120. Epub 2017 Mar 13.

Service of Genetic Medicine, Geneva University Hospitals, Geneva, Switzerland.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.gheart.2017.01.003DOI Listing
June 2017

Challenges in clinical diagnosis of williams-beuren syndrome in sub-saharan africans: case reports from cameroon.

Mol Syndromol 2014 Dec 29;5(6):287-92. Epub 2014 Nov 29.

Faculty of Medicine and Biomedical Sciences, University of Yaoundé I, Yaoundé, Cameroon ; Division of Human Genetics, University of Cape Town, Cape Town, South Africa.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000369421DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4281575PMC
December 2014