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Journal Article
Journal Article
American Journal of Medical Genetics Part A, ISSN 1552-4825, 04/2014, Volume 164, Issue 4, pp. 1079 - 1082
Journal Article
Journal Article
Clinical Anatomy, ISSN 0897-3806, 07/2016, Volume 29, Issue 5, pp. 628 - 632
Trisomy 18 is the second most common aneuploidy after trisomy 21. Due to its multi‐systemic defects, it has a poor prognosis with a 50% chance of survival... 
clenched fist | ventricular septal defect | rocker bottom feet | trisomy 18 | Edward syndrome | MALFORMATIONS | ANATOMY & MORPHOLOGY | Trisomy - diagnosis | Trisomy - genetics | Trisomy - pathology | Chromosomes, Human, Pair 18 - genetics | Prenatal Diagnosis | Trisomy 18 Syndrome
Journal Article
Nature Genetics, ISSN 1061-4036, 06/2015, Volume 47, Issue 6, pp. 577 - 578
Although dietary gluten is the trigger for celiac disease, risk is strongly influenced by genetic variation in the major histocompatibility complex (MHC)... 
HAPLOTYPE | VARIANTS | HLA | ASSOCIATION | HERITABILITY | GENETICS & HEREDITY | Celiac disease | Chromosome mapping | Major histocompatibility complex | Genetic susceptibility | Genetic research | Development and progression | Genetic aspects | Research | Identification and classification | Methods | Studies | Haplotypes | Antigens | Liability | Disease | Genomes | Small intestine
Journal Article
Journal Article
Journal Article
by Speliotes, Elizabeth and Willer, Cristen and Berndt, Sonja and Monda, Keri and Thorleifsson, Gudmar and Jackson, Anne and Allen, H.L and Lindgren, Cecilia and Luan, J and Mägi, Reedik and Randall, Joshua and Vedantam, Sailaja and Winkler, Thomas and Qi, Lu and Workalemahu, Tsegaselassie and Heid, Iris and Steinthorsdottir, Valgerdur and Stringham, Heather and Wheeler, Eleanor and Wood, Anew and Ferreira, Teresa and Weyant, Robert and Segrè, Ayellet and Eestrada, Karol and Liang, Liming and Nemesh, James and Park, J.H and Gustafsson, Stefan and Kilpeläinen, Tuomas and Yang, Joanna and Bouatia-Naji, Nabila and Eesko, Tõnu and Feitosa, Mary Furlan and Kutalik, Zoltán and Mangino, Massimo and Raychaudhuri, Soumya and Scherag, Ane and Smith, Albert Vernon and Welch, Ryan and Zhao, Jing Hua and Aben, Katja and Absher, Devin and Amin, Najaf and Dixon, Anna and Fisher, Eeva and Glazer, Nicole and Goddard, Michael and Heard-Costa, Nancy and Hoesel, Volker and Hottenga, Jouke Jan and Johansson, Åsa and Johnson, Toby and Ketkar, Shamika and Lamina, Claudia and Li, Shengxu and Moffatt, Miriam and Myers, Richard and Narisu, Narisu and Perry, John and Peters, Marjolein and Preuss, Michael and Ripatti, Samuli and Rivadeneira Ramirez, Fernando and Sandholt, Camilla and Scott, Laura and Timpson, Nicholas and Tyrer, Jonathan and Wingerden, Sophie and White, Charles and Wiklund, Freik and Barlassina, Christina and Chasman, Daniel and Cooper, Matthew and Jansson, J.O and Lawrence, Robert and Pellikka, Niina and Prokopenko, Inga and Shi, Jianxin and Thiering, Eelisabeth and Alavere, Helene and Alibrandi, Maria and Almgren, Peter and Arnold, Alice and Aspelund, Thor and Atwood, Larry and Balkau, Beverley and Balmforth, Anthony and Bennett, Amanda and Ben-Shlomo, Y and Bergman, Richard and Bergmann, Sven and Biebermann, Heike and Blakemore, Alexana and Boes, Tanja and Bonnycastle, Lori and Bornstein, Stefan and Brown, Morris and Buchanan, Thomas and Busonero, F and Campbell, Harry and ... and MAGIC and Procardis Consortium and on behalf of Procardis Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature Genetics, ISSN 1061-4036, 11/2010, Volume 42, Issue 11, pp. 937 - 948
Journal Article