Advancing genetic counselling in Southern Africa

From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.

From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.

From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.

From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.

From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.

From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.

From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.

From the Department of Biochemistry, Clinical Pathology and Genetics (Chimpolo, Calumbuana, Kay), Faculty of Medicine, Universidade A. Neto, Hospital Américo Boavida, Luanda; from the Department of Medical Basic Sciences (Chimpolo), Faculty of Medicine, Universidade Katyavala Bwila, University Campus of Catumbela, Benguela;from Division of Molecular Biology and Human Genetics (Moosa), Stellenbosch University, Cape Town, South Africa; from the Institute of Human Genetics, National Institutes of Health and Department of Pediatrics (Silao), College of Medicine and Philippine General Hospital, University of the Philippines-Manila, Manila, Philippines; from Malaysian Node of the Human Variome Project (Halim-Fikri), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia; from the Department of Cardiovascular Genomics (Kumar), William Harvey Research Institute, Bart’s and The London School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom; from the Human Genome Centre (Zilfalil), School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia.