Homozygous Mutations in NEUROD1 Are Responsible for a Novel Syndrome of Permanent Neonatal Diabetes and Neurological Abnormalities von RUBIO-CABEZAS, Oscar, MINTON, Jayne A. L, KANTOR, Iren, WILLIAMS, Denise, ELLARD, Sian, HATTERSLEY, Andrew T

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Wolcott-Rallison Syndrome Is the Most Common Genetic Cause of Permanent Neonatal Diabetes in Consanguineous Families von Rubio-Cabezas, Oscar, Patch, Ann-Marie, Minton, Jayne A. L., Flanagan, Sarah E., Edghill, Emma L., Hussain, Khalid, Balafrej, Amina, Deeb, Asma, Buchanan, Charles R., Jefferson, Ian G., Mutair, Angham, Hattersley, Andrew T., Ellard, Sian

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Clinical Heterogeneity in Patients With FOXP3 Mutations Presenting With Permanent Neonatal Diabetes von Rubio-Cabezas, Oscar, Minton, Jayne A.L, Caswell, Richard, Shield, Julian P, Deiss, Dorothee, Sumnik, Zdenek, Cayssials, Amely, Herr, Mathias, Loew, Anja, Lewis, Vaughan, Ellard, Sian, Hattersley, Andrew T

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Mutation Surveyor: Software for DNA Sequence Analysis von Minton, Jayne A. L., Flanagan, Sarah E., Ellard, Sian

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Association Studies of Genetic Variation in the WFS1 Gene and Type 2 Diabetes in U.K. Populations von MINTON, Jayne A. L, HATTERSLEY, Andrew T, OWEN, Katharine, MCCARTHY, Mark I, WALKER, Mark, LATIF, Farida, BARRETT, Timothy, FRAYLING, Timothy M

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Sequencing of candidate genes selected by beta cell experts in monogenic diabetes of unknown aetiology von Edghill, Emma L, Minton, Jayne A L, Groves, Christopher J, Flanagan, Sarah E, Patch, Ann-Marie, Rubio-Cabezas, Oscar, Shepherd, Maggie, Lenzen, Sigurd, McCarthy, Mark I, Ellard, Sian, Hattersley, Andrew T

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The impact of the angiotensin-converting enzyme insertion/deletion polymorphism on severe hypoglycemia in Type 2 diabetes von Freathy, Rachel M, Lonnen, Kathryn F, Steele, Anna M, Minton, Jayne A L, Frayling, Timothy M, Hattersley, Andrew T, Macleod, Kenneth M

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Characterization of [125I]‐SB‐258585 binding to human recombinant and native 5‐HT6 receptors in rat, pig and human brain tissue von Hirst, Warren D, Minton, Jayne A L, Bromidge, Steven M, Moss, Stephen F, Latter, Alison J, Riley, Graham, Routledge, Carol, Middlemiss, Derek N, Price, Gary W

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Wolfram syndrome von Minton, Jayne A L, Rainbow, Lynne A, Ricketts, Christopher, Barrett, Timothy G

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Characterization of [ 125 I]‐SB‐258585 binding to human recombinant and native 5‐HT 6 receptors in rat, pig and human brain tissue von Hirst, Warren D, Minton, Jayne A L, Bromidge, Steven M, Moss, Stephen F, Latter, Alison J, Riley, Graham, Routledge, Carol, Middlemiss, Derek N, Price, Gary W

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Pharmacological characterisation of a cell line expressing GABAB1b and GABAB2 receptor subunits von HIRST, Warren D, BABBS, Adam J, GREEN, Andrew, MINTON, Jayne A. L, SHAW, Tracy E, WISE, Alan, RICE, Simon Q, PANGALOS, Menelas N, PRICE, Gary W

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Pharmacological characterisation of a cell line expressing GABA B1b and GABA B2 receptor subunits von Hirst, Warren D., Babbs, Adam J., Green, Andrew, Minton, Jayne A.L., Shaw, Tracy E., Wise, Alan, Rice, Simon Q., Pangalos, Menelas N., Price, Gary W.

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Thiamine-responsive megaloblastic anaemia syndrome : Long-term follow-up and mutation analysis of seven families von RICKETTS, Christopher J, MINTON, Jayne A, SAMUEL, Jacob, ARIYAWANSA, Indra, WALES, Jerry K, LO, Ivan F, BARRETT, Timothy G

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