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Lancet (London, England)|June 18, 1988
Simple non-invasive method to obtain DNA for gene analysisN Lench, P Stanier, R WilliamsonBritish Dental Journal|June 24, 1995
Amelogenesis imperfecta in triplets: a unique family recordI Holroyd, N Lench, G B WinterHuman Genetics|November 1, 1988
Detection of a rare-cutter RFLP in a CpG-rich island near the cystic fibrosis locusP Stanier, X Estivill, N Lench, et al.Oral Diseases|March 1, 1995
Nance-Horan syndrome: a contiguous gene syndrome involving deletion of the amelogenin gene? A case report and molecular analysisE Franco, S Hodgson, N Lench, et al.European Journal of Human Genetics : EJHG|April 10, 1999
DFNB20: a novel locus for autosomal recessive, non-syndromal sensorineural hearing loss maps to chromosome 11q25-qterL Moynihan, M Houseman, V Newton, et al.Case Reports in Genetics|August 19, 2017
An Interstitial 4q Deletion with a Mosaic Complementary Ring Chromosome in a Child with Dysmorphism, Linear Skin Pigmentation, and HepatomegalyJ Carter, H Brittain, D Morrogh, et al.Nucleic Acids Research|February 25, 1987
Progress towards construction of a total restriction fragment map of a human chromosomeH Vissing, F Grosveld, E Solomon, et al.Novartis Foundation Symposium|April 20, 1999
Gap junctions and connexin expression in the inner earA Forge, D Becker, S Casalotti, et al.Progress in Clinical and Biological Research|January 1, 1987
The application of molecular genetics to the study of the basic defect causing cystic fibrosisX Estivill, G Bates, G Bell, et al.American Journal of Human Genetics|January 1, 1988
Refined linkage map of chromosome 7 in the region of the cystic fibrosis geneG M Lathrop, M Farrall, P O'Connell, et al.Pageof 2