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A Comparative Study of Hearing Loss in Two Microdeletion Syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) Syndromes |
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| Authors: | Omer Zarchi Josef Attias Eyal Raveh Lina Basel-Vanagaite Liron Saporta Doron Gothelf |
| Affiliation: | a Behavioral Neurogenetics Center, The Edmond and Lily Safra Children’s Hospital, Sheba Medical Center, Tel Hashomer, Israel b Institute for Clinical Neurophysiology and Audiology, Schneider Children’s Medical Center of Israel, Petah Tiqwa, Israel c Department of Otolaryngology and Head and Neck Surgery, Schneider Children’s Medical Center of Israel, Petah Tiqwa, Israel d Department of Communication Disorders, Haifa University, Haifa, Israel e Department of Medical Genetics and Raphael Recanati Genetic Institute, Rabin Medical Center, Petah Tiqwa, Israel f Interdisciplinary Ph.D. Program in Neuroscience Tel Aviv, Israel g Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel |
| Abstract: | |
| Keywords: | AR, Acoustic reflex COMT, Catechol-O-methyltransferase DD, Developmental disability ENT, Ear, nose, and throat SRT, Speech reception threshold TD, Typically developing VCFS, Velocardiofacial syndrome WS, Williams syndrome |
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