Mechanism and isotherm modeling of effective adsorption of malachite green as endocrine disruptive dye using Acid Functionalized Maize Cob (AFMC) von Ojediran, John O, Dada, Adewumi Oluwasogo, Aniyi, Stephen O, David, Robinson O., Adewumi, Adejoke D

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DNA Methylation Profiling of Uniparental Disomy Subjects Provides a Map of Parental Epigenetic Bias in the Human Genome von Joshi, Ricky S., Garg, Paras, Zaitlen, Noah, Lappalainen, Tuuli, Watson, Corey T., Azam, Nidha, Ho, Daniel, Li, Xin, Antonarakis, Stylianos E., Brunner, Han G., Buiting, Karin, Cheung, Sau Wai, Coffee, Bradford, Eggermann, Thomas, Francis, David, Geraedts, Joep P., Gimelli, Giorgio, Jacobson, Samuel G., Le Caignec, Cedric, de Leeuw, Nicole, Liehr, Thomas, Mackay, Deborah J., Montgomery, Stephen B., Pagnamenta, Alistair T., Papenhausen, Peter, Robinson, David O., Ruivenkamp, Claudia, Schwartz, Charles, Steiner, Bernhard, Stevenson, David A., Surti, Urvashi, Wassink, Thomas, Sharp, Andrew J.

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Megalencephaly syndromes: exome pipeline strategies for detecting low-level mosaic mutations von Tapper, William J, Foulds, Nicola, Cross, Nicholas C P, Aranaz, Paula, Score, Joannah, Hidalgo-Curtis, Claire, Robinson, David O, Gibson, Jane, Ennis, Sarah, Temple, I Karen, Collins, Andrew

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Hypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57 von Mackay, Deborah J G, Callaway, Jonathan L A, Marks, Sophie M, White, Helen E, Acerini, Carlo L, Boonen, Susanne E, Dayanikli, Pinar, Firth, Helen V, Goodship, Judith A, Haemers, Andreas P, Hahnemann, Johanne M D, Kordonouri, Olga, Masoud, Ahmed F, Oestergaard, Elsebet, Storr, John, Ellard, Sian, Hattersley, Andrew T, Robinson, David O, Temple, I Karen

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Influence of the MDM2 single nucleotide polymorphism SNP309 on tumour development in BRCA1 mutation carriers von Copson, Ellen R, White, Helen E, Blaydes, Jeremy P, Robinson, David O, Johnson, Peter W, Eccles, Diana M

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Absence of correlation between late-replication and spreading of X inactivation in an X;autosome translocation von SHARP, Andrew, ROBINSON, David O, JACOBS, Patricia

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Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia von Robinson, David O., Howarth, Rachel J., Williamson, Kathleen A., van Heyningen, Veronica, Beal, Sarah J., Crolla, John A.

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Darier disease, multiple bone cysts, and aniridia due to double de novo heterozygous mutations in ATP2A2 and PAX6 von Castori, Marco, Barboni, Luana, Duncan, Philippa J., Paradisi, Mauro, Laino, Luigi, De Bernardo, Carmelilia, Robinson, David O., Grammatico, Paola

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Methylation profiling in individuals with uniparental disomy identifies novel differentially methylated regions on chromosome 15 von Sharp, Andrew J, Migliavacca, Eugenia, Dupre, Yann, Stathaki, Elisavet, Sailani, Mohammad Reza, Baumer, Alessandra, Schinzel, Albert, Mackay, Deborah J, Robinson, David O, Cobellis, Gilda, Cobellis, Luigi, Brunner, Han G, Steiner, Bernhard, Antonarakis, Stylianos E

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A candidate gene for congenital bilateral isolated ptosis identified by molecular analysis of a de novo balanced translocation von MCMULLAN, Tristan F. W, CROLLA, John A, GREGORY, Simon G, CARTER, Nigel P, COOPER, Rachel A, HOWELL, Gareth R, ROBINSON, David O

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Mutations in BMP4 Cause Eye, Brain, and Digit Developmental Anomalies: Overlap between the BMP4 and Hedgehog Signaling Pathways von Bakrania, Preeti, Efthymiou, Maria, Klein, Johannes C., Salt, Alison, Bunyan, David J., Wyatt, Alex, Ponting, Chris P., Martin, Angela, Williams, Steven, Lindley, Victoria, Gilmore, Joanne, Restori, Marie, Robson, Anthony G., Neveu, Magella M., Holder, Graham E., Collin, J Richard O., Robinson, David O., Farndon, Peter, Johansen-Berg, Heidi, Gerrelli, Dianne, Ragge, Nicola K.

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The distinguishing sequence characteristics of mouse imprinted genes von Ke, Xiayi, Thomas, N Simon, Robinson, David O, Collins, Andrew

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Mutations in phospholipase C epsilon 1 are not sufficient to cause diffuse mesangial sclerosis von Gilbert, Rodney D., Turner, Claire L.S., Gibson, Jane, Bass, Paul S., Haq, Mushfequr R., Cross, Esta, Bunyan, David J., Collins, Andrew R., Tapper, William J., Needell, Juliet C., Dell, Beverley, Morton, Newton E., Temple, I. Karen, Robinson, David O.

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An imprinted locus associated with transient neonatal diabetes mellitus von GARDNER, R. J, MACKAY, D. J. G, MUNGALL, A. J, POLYCHRONAKOS, C, SIEBERT, R, SHIELD, J. P. H, TEMPLES, I. K, ROBINSON, D. O

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Next Generation Diagnostics in Inherited Arrhythmia Syndromes: A Comparison of Two Approaches von Ware, James S., John, Shibu, Roberts, Angharad M., Buchan, Rachel, Gong, Sungsam, Peters, Nicholas S., Robinson, David O., Lucassen, Anneke, Behr, Elijah R., Cook, Stuart A.

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Two cases of oculopharyngeal muscular dystrophy (OPMD) with the rare PABPN1 c.35G > C; p.Gly12Ala point mutation von Robinson, David O, Hilton-Jones, David, Mansfield, David, Hildebrand, Göran Darius, Marks, Sophie, Mechan, Dorothy, Ramsay, Joanne

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Molecular genetics external quality assessment pilot scheme for KRAS analysis in metastatic colorectal cancer von Deans, Zandra C, Tull, Justyna, Beighton, Gemma, Abbs, Stephen, Robinson, David O, Butler, Rachel

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Sonic hedgehog mutations are an uncommon cause of developmental eye anomalies von Bakrania, Preeti, Ugur Iseri, Sibel A., Wyatt, Alexander W., Bunyan, Dave J., Lam, Wayne W.K., Salt, Alison, Ramsay, Jacqueline, Robinson, David O., Ragge, Nicola K.

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Donnai–Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy von Kantarci, Sibel, Ragge, Nicola K., Thomas, N. Simon, Robinson, David O., Noonan, Kristin M., Russell, Meaghan K., Donnai, Dian, Raymond, F. Lucy, Walsh, Christopher A., Donahoe, Patricia K., Pober, Barbara R.

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Molecular and cytogenetic analysis of the spreading of X inactivation in X;autosome translocations von Sharp, Andrew J., Spotswood, Hugh T., Robinson, David O., Turner, Bryan M., Jacobs, Patricia A.

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