HuGE Literature Finder
Records 1-2
Frequency of Usher syndrome in two pediatric populations: Implications for genetic screening of deaf and hard of hearing children.
Genetics in medicine : official journal of the American College of Medical Genetics 2010 Aug 12 (8): 512-6. Kimberling William J, Hildebrand Michael S, Shearer A Eliot, Jensen Maren L, Halder Jennifer A, Trzupek Karmen, Cohn Edward S, Weleber Richard G, Stone Edwin M, Smith Richard J |
The R245X mutation of PCDH15 in Ashkenazi Jewish children diagnosed with nonsyndromic hearing loss foreshadows retinitis pigmentosa.
Pediatric research 2004 Jun 55 (6): 995-1000. Brownstein Zippora, Ben-Yosef Tamar, Dagan Orit, Frydman Moshe, Abeliovich Dvorah, Sagi Michal, Abraham Fabian A, Taitelbaum-Swead Riki, Shohat Mordechai, Hildesheimer Minka, Friedman Thomas B, Avraham Karen |
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- Page last updated:Jan 19, 2021
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