检索结果 - Mohammad Amin Tabatabaiefar
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A Mutation in CABP2 , Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment 由 Isabelle Schrauwen, Sarah Helfmann, Akira Inagaki, Friederike Predoehl, Mohammad Amin Tabatabaiefar, Maria Magdalena Picher, Manou Sommen, Celia Zazo Seco, Jaap Oostrik, Hannie Kremer, Annelies Dheedene, Charlotte Claes, Erik Fransén, Morteza Hashemzadeh Chaleshtori, Paul Coucke, Amy Lee, Tobias Moser, Guy Van Camp
出版 2012Artigo -
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Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform 由 Sarah De Keulenaer, Jan Hellemans, Steve Lefever, Jean‐Pierre Renard, Joachim De Schrijver, Hendrik Van de Voorde, Mohammad Amin Tabatabaiefar, Filip Van Nieuwerburgh, Daisy Flamez, Filip Pattyn, Bieke Scharlaken, Dieter Deforce, Sofie Bekaert, Wim Van Criekinge, Jo Vandesompele, Guy Van Camp, Paul Coucke
出版 2012Artigo -
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A Versatile Biomimic Nanotemplating Fluidic Assay for Multiplex Quantitative Monitoring of Viral Respiratory Infections and Immune Responses in Saliva and Blood 由 Roozbeh Siavash Moakhar, Carolina del Real Mata, Mahsa Jalali, Houda Shafique, Alireza Sanati, Justin de Vries, Julia Strauss, Tamer AbdElFatah, Fahimeh Ghasemi, Myles McLean, Imman I. Hosseini, Yao Lü, Sripadh Guptha Yedire, Sara Mahshid, Mohammad Amin Tabatabaiefar, Chen Liang, Sara Mahshid
出版 2022Artigo
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