Zobrazeno 1 - 2
of 2
pro vyhledávání: '"C. R.S. Srisailapathy"'
Autor:
Cynthia C. Morton, Anne B. Skvorak, Rivka Carmi, Ross I. S. Zbar, M Musy, Khalil Elbedour, M. L. Kraft, C. R.S. Srisailapathy, Richard J.H. Smith, Val C. Sheffield, Jacquie Marietta, Arabandi Ramesh, Michael Lovett, Jose M. Manaligod, G. Van Camp, Y. Yairi, Daryl A. Scott, John H. Greinwald
Publikováno v:
Genome Research. 7:879-886
DFNB7 and DFNB11, two loci for autosomal recessive nonsyndromic hearing loss (ARNSHL), have been mapped to chromosome 9q13–21 in separate consanguineous families. Using a radiation hybrid map, we have determined the correct marker order in the DFNB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ed3d76fb18b2bf052fbb3f1f44ed2fb
https://doi.org/10.1101/gr.7.9.879
https://doi.org/10.1101/gr.7.9.879
Autor:
P. Jain, Li Ni, Arabandi Ramesh, Sigrid Wayne, Ross I. S. Zbar, P. Coucke, Judith B. Kenyon, C. R.S. Srisailapathy, E. R. Wilcox, G. Van Camp, Shelley D. Smith, Richard J.H. Smith, Kunihiro Fukushima, Michelle O'Neill
Publikováno v:
Genome research
Scopus-Elsevier
Scopus-Elsevier
Autosomal recessive nonsyndromic hearing loss (ARNSHL) is the most common form of congenitally acquired inherited hearing impairment. Although numerous loci are believed to exist, only five have been identified. Using a pooled genomic DNA screening s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f2aaf66554dd6d68608379b681df81a
https://pubmed.ncbi.nlm.nih.gov/8593615
https://pubmed.ncbi.nlm.nih.gov/8593615