Items where Author is "Schrauwen, Isabelle."

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Schrauwen, Isabelle. and Helfmann, Sarah. and Inagaki, Akira. and Predoehl, Friederike. and Tabatabaiefar, Mohammad Amin. and Magdalena Picher, Maria. and Sommen, Manou. and Seco, Celia Zazo and Oostrik, Jaap. and Kremer, Hannie. and Dheedene, Annelies. and Claes, Charlotte. and Fransen, Erik. and Hashemzadeh Chaleshtori, Morteza. and Coucke, Paul. and Lee, Amy. and Moser, Tobias. and Van Camp, Guy. (2012) A Mutation in CABP2, Expressed in Cochlear Hair Cells, Causes Autosomal-Recessive Hearing Impairment. AMERICAN JOURNAL OF HUMAN GENETICS, 91 (4). pp. 636-645.

Vanwesemael, Maarten. and Schrauwen, Isabelle. and Ceuppens, Ruben. and Alasti, Fatemeh. and Jorssen, Ellen. and Farrokhi, Effat. and Hashemzadeh-Chaleshtori, Morteza. and Van Camp, Guy. (2011) A 1 bp Deletion in the Dual Reading Frame Deafness Gene LRTOMT Causes a Frameshift From the First Into the Second Reading Frame. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 155A (8). pp. 2021-2023.

This list was generated on Mon Apr 6 01:09:35 2020 IRDT.