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

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

Volume 12 (2017): Issue 2

By: Ambroise Wonkam, Ricardo Toko, David Chelo, Cedrik Tekendo-Ngongang, Samuel Kingue and Sophie Dahoun

Open Access

|Jun 2017

Authors

Ambroise Wonkam

ambroise.wonkam@uct.ac.za

Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town

Ricardo Toko

info@ubiquitypress.com

Faculty of Medicine and Biomedical Sciences, University of Yaoundé 1, Yaoundé

David Chelo

info@ubiquitypress.com

Faculty of Medicine and Biomedical Sciences, University of Yaoundé 1, Yaoundé

Cedrik Tekendo-Ngongang

info@ubiquitypress.com

Division of Human Genetics, Faculty of Health Sciences, University of Cape Town, Cape Town

Samuel Kingue

info@ubiquitypress.com

Faculty of Medicine and Biomedical Sciences, University of Yaoundé 1, Yaoundé

Sophie Dahoun

info@ubiquitypress.com

Service of Genetic Medicine, Geneva University Hospitals, Geneva

DOI: https://doi.org/10.1016/j.gheart.2017.01.003 | Journal eISSN: 2211-8179

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Language: English

Published on: Jun 1, 2017

Published by: Ubiquity Press

In partnership with: Paradigm Publishing Services

Publication frequency: 1 issue per year

© 2017 Ambroise Wonkam, Ricardo Toko, David Chelo, Cedrik Tekendo-Ngongang, Samuel Kingue, Sophie Dahoun, published by Ubiquity Press
This work is licensed under the Creative Commons Attribution 4.0 License.

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