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1دورية أكاديمية
المؤلفون: Farlie, PG, Davidson, NM, Baker, NL, Raabus, M, Roeszler, KN, Hirst, C, Major, A, Mariette, MM, Lambert, DM, Oshlack, A, Smith, CA
العلاقة: pii: 10.1038/s41467-017-00112-7; Farlie, P. G., Davidson, N. M., Baker, N. L., Raabus, M., Roeszler, K. N., Hirst, C., Major, A., Mariette, M. M., Lambert, D. M., Oshlack, A. & Smith, C. A. (2017). Co-option of the cardiac transcription factor Nkx2 . 5 during development of the emu wing. NATURE COMMUNICATIONS, 8 (1), https://doi.org/10.1038/s41467-017-00112-7Test.; http://hdl.handle.net/11343/256478Test
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2دورية أكاديمية
المؤلفون: Smith, CA, Farlie, PG, Davidson, NM, Roeszler, KN, Hirst, C, Oshlack, A, Lambert, DM
العلاقة: pii: 63; Smith, C. A., Farlie, P. G., Davidson, N. M., Roeszler, K. N., Hirst, C., Oshlack, A. & Lambert, D. M. (2016). Limb patterning genes and heterochronic development of the emu wing bud. EVODEVO, 7 (1), https://doi.org/10.1186/s13227-016-0063-5Test.; http://hdl.handle.net/11343/257844Test
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3دورية أكاديمية
المؤلفون: Miller, KA, Gordon, CT, Welfare, MF, Caruana, G, Bertram, JF, Bateman, JF, Farlie, PG
المساهمون: Kappen, C
العلاقة: pii: PONE-D-13-21478; Miller, K. A., Gordon, C. T., Welfare, M. F., Caruana, G., Bertram, J. F., Bateman, J. F. & Farlie, P. G. (2013). bfb, a Novel ENU-Induced blebs Mutant Resulting from a Missense Mutation in Fras1. PLOS ONE, 8 (10), https://doi.org/10.1371/journal.pone.0076342Test.; http://hdl.handle.net/11343/261169Test
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4دورية أكاديمية
المؤلفون: Miller, KA, Ah-Cann, CJ, Welfare, MF, Tan, TY, Pope, K, Caruana, G, Freckmann, M-L, Savarirayan, R, Bertram, JF, Dobbie, MS, Bateman, JF, Farlie, PG
المساهمون: Dutcher, SK
العلاقة: pii: PGENETICS-D-13-00047; Miller, K. A., Ah-Cann, C. J., Welfare, M. F., Tan, T. Y., Pope, K., Caruana, G., Freckmann, M. -L., Savarirayan, R., Bertram, J. F., Dobbie, M. S., Bateman, J. F. & Farlie, P. G. (2013). Cauli: A Mouse Strain with an Ift140 Mutation That Results in a Skeletal Ciliopathy Modelling Jeune Syndrome. PLOS GENETICS, 9 (8), https://doi.org/10.1371/journal.pgen.1003746Test.; http://hdl.handle.net/11343/265547Test
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5دورية أكاديمية
المؤلفون: Caruana, G, Farlie, PG, Hart, AH, Bagheri-Fam, S, Wallace, MJ, Dobbie, MS, Gordon, CT, Miller, KA, Whittle, B, Abud, HE, Arkell, RM, Cole, TJ, Harley, VR, Smyth, IM, Bertram, JF
المساهمون: Veitia, RA
العلاقة: pii: PONE-D-12-31938; Caruana, G., Farlie, P. G., Hart, A. H., Bagheri-Fam, S., Wallace, M. J., Dobbie, M. S., Gordon, C. T., Miller, K. A., Whittle, B., Abud, H. E., Arkell, R. M., Cole, T. J., Harley, V. R., Smyth, I. M. & Bertram, J. F. (2013). Genome-Wide ENU Mutagenesis in Combination with High Density SNP Analysis and Exome Sequencing Provides Rapid Identification of Novel Mouse Models of Developmental Disease. PLOS ONE, 8 (3), https://doi.org/10.1371/journal.pone.0055429Test.; http://hdl.handle.net/11343/265429Test
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6دورية أكاديمية
المؤلفون: Cameron, TL, Belluoccio, D, Farlie, PG, Brachvogel, B, Bateman, JF
العلاقة: pii: 1471-213X-9-20; Cameron, T. L., Belluoccio, D., Farlie, P. G., Brachvogel, B. & Bateman, J. F. (2009). Global comparative transcriptome analysis of cartilage formation in vivo . BMC DEVELOPMENTAL BIOLOGY, 9 (1), https://doi.org/10.1186/1471-213X-9-20Test.; http://hdl.handle.net/11343/242932Test
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7دورية أكاديمية
المؤلفون: Jones, NC, Farlie, PG, Minichiello, J, Newgreen, DF
مصطلحات موضوعية: ARTICLES
وصف الملف: text/html
العلاقة: http://hmg.oxfordjournals.org/cgi/content/short/8/12/2239Test; http://dx.doi.org/10.1093/hmg/8.12.2239Test
الإتاحة: https://doi.org/10.1093/hmg/8.12.2239Test
http://hmg.oxfordjournals.org/cgi/content/short/8/12/2239Test -
8دورية أكاديمية
المؤلفون: Logjes, RJH, Breugem, CC, Van Haaften, G, Paes, EC, Sperber, GH, van den Boogaard, M-JH, Farlie, PG
العلاقة: Logjes, R. J. H., Breugem, C. C., Van Haaften, G., Paes, E. C., Sperber, G. H., van den Boogaard, M. -J. H. & Farlie, P. G. (2018). The ontogeny of Robin sequence. AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 176 (6), pp.1349-1368. https://doi.org/10.1002/ajmg.a.38718Test.; http://hdl.handle.net/11343/284055Test
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9دورية أكاديمية
المؤلفون: Breugem, CC, Evans, KN, Poets, CF, Suri, S, Picard, A, Filip, C, Paes, EC, Mehendale, FV, Saal, HM, Basart, H, Murthy, J, Joosten, Koen, Speleman, L, Collares, MVM, van den Boogaard, MJH, Muradin, M, Andersson, MEM, Kogo, M, Farlie, PG, Griot, PD, Mossey, PA, Slator, R, Abadie, V, Hong, P
المصدر: Breugem , CC , Evans , KN , Poets , CF , Suri , S , Picard , A , Filip , C , Paes , EC , Mehendale , FV , Saal , HM , Basart , H , Murthy , J , Joosten , K , Speleman , L , Collares , MVM , van den Boogaard , MJH , Muradin , M , Andersson , MEM , Kogo , M , Farlie , PG , Griot , PD , Mossey , PA , Slator , R , Abadie , V & Hong , P 2016 , ....
الإتاحة: https://doi.org/10.1001/jamapediatrics.2016.0796Test
https://pure.eur.nl/en/publications/3f096e6c-747d-4955-b3ab-3894c6b3d700Test -
10دورية أكاديمية
المؤلفون: Amor, DJ, Tan, TY, Collins, A, James, PA, Mcgillivray, G, Stark, Z, Gordon, CT, Leventer, RJ, Pope, K, Forbes, R, Crolla, JA, Ganesamoorthy, D, Burgess, T, Bruno, DL, Slater, HR, Farlie, PG
مصطلحات موضوعية: Adolescent, Adult, Child, Preschool, Chromosomes, Human, Pair 22 - Genetics, Dna Copy Number Variations - Genetics, Female, Genetic Association Studies, Goldenhar Syndrome - Genetics, Humans, Infant, Newborn, Male, Phenotype, Repetitive Sequences, Nucleic Acid - Genetics, Young Adult
العلاقة: American Journal of Medical Genetics, Part A; http://www.scopus.com/mlt/select.url?eid=2-s2.0-79959534034&selection=ref&src=s&origin=recordpageTest; American Journal Of Medical Genetics, Part A, 2011, v. 155 n. 7, p. 1623-1633; 1633; WOS:000291944700020; eid_2-s2.0-79959534034; 1623; http://hdl.handle.net/10722/170452Test; 155
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