المؤلفون: Adhya, D, Swarup, V, Nagy, R, Dutan, L, Shum, C, Valencia-Alarcón, EP, Jozwik, KM, Mendez, MA, Horder, J, Loth, E, Nowosiad, P, Lee, I, Skuse, D, Flinter, FA, Murphy, D, McAlonan, G, Geschwind, DH, Price, J, Carroll, J, Srivastava, DP, Baron-Cohen, S

المصدر: Biological Psychiatry , 89 (5) pp. 486-496. (2021)

مصطلحات موضوعية: Autism, Cortical differentiation, Functional genomics, Midbrain differentiation, Neural precursors, Neural progenitor cells, Neurodevelopment

وصف الملف: text

العلاقة: https://discovery.ucl.ac.uk/id/eprint/10108530/7/Lee_Atypical%20Neurogenesis%20in%20Induced%20Pluripotent%20Stem%20Cells%20From%20Autistic%20Individuals_VoR.pdfTest; https://discovery.ucl.ac.uk/id/eprint/10108530Test/

الإتاحة: https://discovery.ucl.ac.uk/id/eprint/10108530/7/Lee_Atypical%20Neurogenesis%20in%20Induced%20Pluripotent%20Stem%20Cells%20From%20Autistic%20Individuals_VoR.pdfTest
https://discovery.ucl.ac.uk/id/eprint/10108530Test/

المؤلفون: Rheault, MN, Savige, J, Randles, MJ, Weinstock, A, Stepney, M, Turner, AN, Parziale, G, Gross, O, Flinter, FA, Miner, JH, Lagas, S, Gear, S, Lennon, R

العلاقة: pii: 10.1007/s00467-019-04241-7; Rheault, M. N., Savige, J., Randles, M. J., Weinstock, A., Stepney, M., Turner, A. N., Parziale, G., Gross, O., Flinter, F. A., Miner, J. H., Lagas, S., Gear, S. & Lennon, R. (2020). The importance of clinician, patient and researcher collaborations in Alport syndrome. PEDIATRIC NEPHROLOGY, 35 (5), pp.733-742. https://doi.org/10.1007/s00467-019-04241-7Test.; http://hdl.handle.net/11343/247540Test

الإتاحة: https://doi.org/10.1007/s00467-019-04241-7Test
http://hdl.handle.net/11343/247540Test

المؤلفون: Wei, W, Tuna, S, Keogh, MJ, Smith, KR, Aitman, TJ, Beales, PL, Bennett, DL, Gale, DP, Bitner-Glindzicz, MAK, Black, GC, Brennan, P, Elliott, P, Flinter, FA, Floto, RA, Houlden, H, Irving, M, Koziell, A, Maher, ER, Markus, HS, Morrell, NW, Newman, WG, Roberts, I, Sayer, JA, Smith, KGC, Taylor, JC, Watkins, H, Webster, AR, Wilkie, AOM, Williamson, C, Diseases, NIHR BioResource–Rare, Pilot, 100,000 Genomes Project–Rare Diseases, Ashford, S, Penkett, CJ, Stirrups, KE, Rendon, A, Ouwehand, WH, Bradley, JR, Raymond, FL, Caulfield, M, Turro, E, Chinnery, PF

العلاقة: https://ora.ox.ac.uk/objects/uuid:8c4c93aa-8c16-456b-8346-d05af30b4b1bTest; https://doi.org/10.1126/science.aau6520Test

الإتاحة: https://doi.org/10.1126/science.aau6520Test
https://ora.ox.ac.uk/objects/uuid:8c4c93aa-8c16-456b-8346-d05af30b4b1bTest

المؤلفون: Rheault, MN, Savige, J, Randles, MJ, Weinstock, A, Stepney, M, Turner, AN, Parziale, G, Gross, O, Flinter, FA, Miner, JH, Lagas, S, Gear, S, Lennon, R

العلاقة: https://ora.ox.ac.uk/objects/uuid:00805d8b-0e8a-4cbc-aff4-8af8ea1ff35dTest; https://doi.org/10.1007/s00467-019-04241-7Test

الإتاحة: https://doi.org/10.1007/s00467-019-04241-7Test
https://ora.ox.ac.uk/objects/uuid:00805d8b-0e8a-4cbc-aff4-8af8ea1ff35dTest

المؤلفون: King, K, Flinter, FA, Green, PM

المصدر: King , K , Flinter , FA & Green , PM 2006 , ' A two-tier approach to mutation detection in the COL4A5 gene for Alport Syndrome ' , Human Mutation , vol. 27 , no. 10 , 924 , pp. 1061 . https://doi.org/10.1002/humu.9453Test

الإتاحة: https://doi.org/10.1002/humu.9453Test
https://kclpure.kcl.ac.uk/portal/en/publications/a-twotier-approach-to-mutation-detection-in-the-col4a5-gene-for-alport-syndromeTest(5a358dbd-1e82-455e-8df2-3a5616f52ba6).html

المؤلفون: Kerecuk L, Sajoo A, McGregor L, Berg J, Haq MR, Sebire NJ, Bingham C, Edghill EL, Ellard S, Taylor J, Rigden S, Flinter FA, Woolf AS

وصف الملف: text; application/pdf

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=od______2295::c90587f7ccf08ea5ad1bed18b085dd87Test
http://www.manchester.ac.uk/escholar/uk-ac-man-scw:78019Test

المؤلفون: Feather, SA, Malcolm, S., Woolf, AS, Wright, V, Blaydon, D, Reid, CJD, Flinter, FA, Proesmans, W., Devriendt, Koenraad, Carter, J, Warwicker, P, Goodship, THJ, Goodship, JA

المساهمون: UCL

المصدر: American Journal of Human Genetics, Vol. 66, no. 4, p. 1420-1425 (2000)

العلاقة: boreal:43422; http://hdl.handle.net/2078.1/43422Test; urn:ISSN:0002-9297; urn:EISSN:1537-6605

الإتاحة: https://doi.org/10.1086/302864Test
http://hdl.handle.net/2078.1/43422Test

المؤلفون: Elcioglu, N, Flinter, FA, Woolf, AS, Parker, D, Beales, PL

المساهمون: 123394

مصطلحات موضوعية: Yaşam Bilimleri, Moleküler Biyoloji ve Genetik, Temel Bilimler, Dahili Tıp Bilimleri, Tıbbi Genetik, Sağlık Bilimleri, Tıp, Yaşam Bilimleri (LIFE), GENETİK VE HAYAT

العلاقة: JOURNAL OF MEDICAL GENETICS; Beales P., Elcioglu N., Woolf A., Parker D., Flinter F., "New criteria for improved diagnosis of Bardet-Biedl syndrome: results of a population survey", JOURNAL OF MEDICAL GENETICS, cilt.36, sa.6, ss.437-446, 1999; vv_1032021; av_6b5f54ef-d9ab-46d9-94b1-aea9b9bf333b; http://hdl.handle.net/20.500.12627/74252Test; 36; 437; 446

الإتاحة: https://doi.org/20.500.12627/74252Test
https://hdl.handle.net/20.500.12627/74252Test