Case Report: An Infant With Kabuki Syndrome, Alobar Holoprosencephaly and Truncus Arteriosus: A Case for Whole Exome Sequencing in Neonates With Congenital Anomalies

por Rishika P. Sakaria, Rishika P. Sakaria, Parul G. Zaveri, Parul G. Zaveri, Shannon Holtrop, Jie Zhang, Jie Zhang, Chester W. Brown, Chester W. Brown, Eniko K. Pivnick, Eniko K. Pivnick
Publicado 2021

Unmapped exome reads implicate a role for Anelloviridae in childhood HIV-1 long-term non-progression

por Savannah Mwesigwa, Lesedi Williams, Gaone Retshabile, Eric Katagirya, Gerald Mboowa, Busisiwe Mlotshwa, Samuel Kyobe, David P. Kateete, Eddie Mujjwiga Wampande, Misaki Wayengera, Sununguko Wata Mpoloka, Angella N. Mirembe, Ishmael Kasvosve, Koketso Morapedi, Grace P. Kisitu, Adeodata R. Kekitiinwa, Gabriel Anabwani, Moses L. Joloba, Enock Matovu, Julius Mulindwa, Harry Noyes, Gerrit Botha, Collaborative African Genomics Network (CAfGEN), TrypanoGEN Research Group, Chester W. Brown, Graeme Mardon, Mogomotsi Matshaba, Neil A. Hanchard
Publicado 2021