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Lancet (London, England)|June 18, 1988
Simple non-invasive method to obtain DNA for gene analysisN Lench, P Stanier, R WilliamsonHuman 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.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.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.Genomics|September 1, 1993
The localization of a gene causing X-linked cleft palate and ankyloglossia (CPX) in an Icelandic kindred is between DXS326 and DXYS1XP Stanier, S A Forbes, A Arnason, et al.Clinical Genetics|December 6, 2017
A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephalyM Ishida, T Cullup, C Boustred, et al.Prenatal Diagnosis|March 1, 1987
Two unusual cases of first trimester prenatal diagnosis of cystic fibrosis using DNA probesH Y Law, P Stanier, R Williamson, et al.British Dental Journal|June 24, 1995
Amelogenesis imperfecta in triplets: a unique family recordI Holroyd, N Lench, G B WinterGenomics|June 1, 1991
Cloning the mouse homolog of the human cystic fibrosis transmembrane conductance regulator geneF Tata, P Stanier, C Wicking, et al.Journal of Medical Genetics|August 4, 2009
A functional haplotype variant in the TBX22 promoter is associated with cleft palate and ankyloglossiaE Pauws, G E Moore, P StanierPageof 202