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Items where Division is "Current Faculties > Faculty of Medicine > Human Development and Health > Human Genetics and Genomic Medicine
Human Development and Health > Human Genetics and Genomic Medicine" and Year is 2017

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Group by: No Grouping | Authors/Creators | Item Type
Jump to: B | C | D | K | L | S
Number of items: 8.

B

Ten considerations for implementing effective and sustainable near-peer teaching in clinical anatomy education - Scott Border, William J.C. Parton, Matthew A. Myers, Ahmad Elmansouri, Johnny Stephens, Eleanor Seaby and Samuel Hall
Type: Article | 2017 | Item not available on this server.

C

Metabolic profiling of polycystic ovary syndrome reveals interactions with abdominal obesity - A. Couto Alves, B. Valcarcel, V.-P. Mäkinen, L. Morin-Papunen, S. Sebert, A.J. Kangas, P. Soininen, S. Das, M. De Iorio, L. Coin, M. Ala-Korpela, M.-R. Järvelin and S. Franks
Type: Article | 2017

D

Type: Article | 2017 | Item availability restricted.

K

Shared genetic variants suggest common pathways in allergy and autoimmune diseases - E. Kreiner, J. Waage, M. Standl, S. Brix, T.H. Pers, A. Couto Alves, N.M. Warrington, C.M.T. Tiesler, E. Fuertes, L. Franke, J.N. Hirschhorn, A. James, A. Simpson, J.Y. Tung, G.H. Koppelman, D.S. Postma, C.E. Pennell, M.-R. Jarvelin, A. Custovic, N. Timpson, M.A. Ferreira, D.P. Strachan, J. Henderson, D. Hinds, H. Bisgaard and K. Bønnelykke
Type: Article | 2017 | Item availability restricted.

A functional SNP associated with atopic dermatitis controls cell type-specific methylation of the VSTM1 gene locus - D. Kumar, K.J. Puan, A.K. Andiappan, B. Lee, G.H.A. Westerlaken, D. Haase, R. Melchiotti, Z. Li, N. Yusof, J. Lum, G. Koh, S. Foo, J. Yeong, A.C. Alves, J. Pekkanen, L.D. Sun, A. Irwanto, B.P. Fairfax, V. Naranbhai, J.E.A. Common, M. Tang, C.K. Chuang, M.-R. Jarvelin, J.C. Knight, X. Zhang, F.T. Chew, S. Prabhakar, L. Jianjun, D.Y. Wang, F. Zolezzi, M. Poidinger, E.B. Lane, L. Meyaard and O. Rötzschke
Type: Article | 2017

L

Type: Article | 2017 | Item not available on this server.

S

Sporadic, isolated Fanconi syndrome due to a mutation of EHHADH: a case report - Eleanor Seaby, David J. Bunyan, Sarah Ennis and Rodney D. Gilbert
Type: Article | 2017

Unexpected Findings in a Child with Atypical Hemolytic Uremic Syndrome: An Example of How Genomics Is Changing the Clinical Diagnostic Paradigm - Eleanor G. Seaby, Rodney D. Gilbert, Gaia Andreoletti, Reuben J Pengelly, Catherine Mercer, David Hunt and Sarah Ennis
Type: Article | 2017

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