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Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|July 10, 2003
Modeling open-set spoken word recognition in postlingually deafened adults after cochlear implantation: some preliminary results with the neighborhood activation modelTed A Meyer, Stefan A Frisch, David B Pisoni, et al.
Vox Sanguinis|September 24, 2010
Influence of late irradiation on the in vitro RBC storage variables of leucoreduced RBCs in SAGM additive solutionR Zimmermann, A M Schoetz, A Frisch, et al.
American Journal of Medical Genetics|July 24, 1998
Linkage disequilibrium of common Gaucher disease mutations with a polymorphic site in the pyruvate kinase (PKLR) geneR Rockah, R Narinsky, M Frydman, et al.
Annals of Neurology|May 1, 1997
Juvenile-onset spinal muscular atrophy caused by compound heterozygosity for mutations in the HEXA geneR Navon, R Khosravi, J Melki, et al.
Neurology|March 1, 1995
A new mutation in the HEXA gene associated with a spinal muscular atrophy phenotypeR Navon, R Khosravi, T Korczyn, et al.
Medical and Pediatric Oncology|April 1, 1996
Vincristine treatment triggering the expression of asymptomatic Charcot-Marie-Tooth diseaseY Neumann, A Toren, G Rechavi, et al.
Israel Journal of Medical Sciences|October 1, 1992
The autosomal dominant polycystic kidney disease gene in a Jewish family from Uzbekistan is PKD1A Frisch, M Frydman, O Blau, et al.
Nature|September 27, 2019
Milk of ruminants in ceramic baby bottles from prehistoric child gravesJ Dunne, K Rebay-Salisbury, R B Salisbury, et al.
Molecular Psychiatry|June 21, 2007
Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish familiesT Venken, M Alaerts, D Souery, et al.
TAG. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik|June 5, 2003
Construction and utility of 10-kb libraries for efficient clone-gap closure for rice genome sequencingTae-Jin Yang, Yeisoo Yu, Gyoungju Nah, et al.
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