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European Journal of Human Genetics : EJHG|October 31, 2002
Genomic rearrangements of EYA1 account for a large fraction of families with BOR syndromeVirginie S Vervoort, Richard J H Smith, Jane O'Brien, et al.Cytopathology : Official Journal of the British Society for Clinical Cytology|April 2, 1998
Guidelines for anal cytology--to make cytological diagnosis and follow up much more reliableJ H Scholefield, J Johnson, A Hitchcock, et al.The Annals of Otology, Rhinology, and Laryngology|June 15, 2007
H-type congenital tracheoesophageal fistula: University Of Iowa experience 1985 to 2005James T Brookes, Mark C Smith, Richard J H Smith, et al.Nature Reviews. Genetics|December 20, 2011
Genomically humanized mice: technologies and promisesAnny Devoy, Rosie K A Bunton-Stasyshyn, Victor L J Tybulewicz, et al.Microbial & Comparative Genomics|February 23, 1999
An efficient, automatable template preparation for high throughput sequencingM Engelstein, T J Aldredge, D Madan, et al.The Annals of Otology, Rhinology, and Laryngology|November 10, 2009
Unilateral vocal fold paralysis in premature infants after ligation of patent ductus arteriosus: vascular clip versus suture ligatureWilliam C Spanos, James T Brookes, Mark C Smith, et al.Biophysical Journal|June 3, 2009
Col11a2 deletion reveals the molecular basis for tectorial membrane mechanical anisotropyKinuko Masaki, Jianwen Wendy Gu, Roozbeh Ghaffari, et al.Journal of the American Society of Nephrology : JASN|September 14, 2013
Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndromeFengxiao Bu, Tara Maga, Nicole C Meyer, et al.Journal of Psychosomatic Research|January 1, 1993
Non-alimentary aspects of the irritable bowel syndromeH Nyhlin, M J Ford, J Eastwood, et al.American Journal of Human Genetics|May 12, 2009
Mutations of KCNJ10 together with mutations of SLC26A4 cause digenic nonsyndromic hearing loss associated with enlarged vestibular aqueduct syndromeTao Yang, Jose G Gurrola, Hao Wu, et al.Pageof 71