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American Journal of Human Genetics|April 25, 2000
A novel locus (DFNA23) for prelingual autosomal dominant nonsyndromic hearing loss maps to 14q21-q22 in a Swiss German kindredA A Salam, F M Häfner, T E Linder, et al.Catheterization and Cardiovascular Diagnosis|June 1, 1993
Contrast echocardiography during cardiac catheterization in patients with congenital heart diseasesJ L Andrade, S M Leal, O Campos Filho, et al.Clinical Genetics|December 25, 2004
Low prevalence of Connexin 26 (GJB2) variants in Pakistani families with autosomal recessive non-syndromic hearing impairmentR L P Santos, M Wajid, T L Pham, et al.HNO|November 17, 1998
[Hereditary deafness in Turkey. Initial results]F Apaydin, M Pfister, M Iber, et al.Clinical Genetics|August 16, 2005
Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB55 to chromosome 4q12-q13.2S Irshad, R L P Santos, D Muhammad, et al.Genetic Epidemiology|January 1, 1997
False positive rates in a genomic screen for complex quantitative traitsW K Scott, M C Speer, S M Leal, et al.Genomics|October 1, 1990
Multipoint linkage analysis and heterogeneity testing in 20 X-linked retinitis pigmentosa familiesM A Musarella, L Anson-Cartwright, S M Leal, et al.Microbiology Spectrum|January 23, 2023
Test Performance and Potential Clinical Utility of the GenMark Dx ePlex Blood Culture Identification Gram-Negative PanelT P McCarty, P Cumagun, J Meeder, et al.Genome Research|May 1, 1996
Genetic and physical mapping of the progressive epilepsy with mental retardation (EPMR) locus on chromosome 8pS Ranta, A E Lehesjoki, A Hirvasniemi, et al.American Journal of Human Genetics|March 31, 2000
A novel locus (DFNA24) for prelingual nonprogressive autosomal dominant nonsyndromic hearing loss maps to 4q35-qter in a large Swiss German kindredF M Häfner, A A Salam, T E Linder, et al.Pageof 8