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American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 2007, Volume 197, Issue 1, pp. 45.e1 - 45.e5
Journal Article
Gut, ISSN 0017-5749, 03/2017, Volume 66, Issue 3, pp. 464 - 472
ObjectiveEstimates of cancer risk and the effects of surveillance in Lynch syndrome have been subject to bias, partly through reliance on retrospective... 
Cancer genetics | cancer syndromes | colorectal cancer | cancer prevention | colonoscopy | MSH2 MUTATION | IMPACT | MANAGEMENT | NONPOLYPOSIS COLORECTAL-CANCER | MUTATION CARRIERS | FAMILIES | GUIDELINES | RISK | MISMATCH REPAIR | GASTROENTEROLOGY & HEPATOLOGY | ADENOMAS | CANCER SYNDROMES | COLONOSCOPY | MLH1 protein | Colorectal carcinoma | MSH2 protein | Sex | COLORECTAL CANCER | Survival | Ovarian cancer | MSH6 protein | Databases | CANCER GENETICS | Death | Mutation | CANCER PREVENTION | Digestive tract | Genetic counselling | Endometrium | Age | Prospective Studies | Age Factors | Endometrial Neoplasms - mortality | Humans | Middle Aged | Male | Ovarian Neoplasms - mortality | Incidence | Colorectal Neoplasms, Hereditary Nonpolyposis - diagnostic imaging | Young Adult | Colorectal Neoplasms, Hereditary Nonpolyposis - mortality | Colonoscopy | Aged, 80 and over | Adult | Female | Child | Databases, Factual | Gene Expression | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Survival Rate | MutS Homolog 2 Protein - genetics | Endometrial Neoplasms - epidemiology | DNA-Binding Proteins - genetics | Ovarian Neoplasms - epidemiology | Colorectal Neoplasms, Hereditary Nonpolyposis - epidemiology | MutL Protein Homolog 1 - genetics | Adolescent | Heterozygote | Aged | Mismatch Repair Endonuclease PMS2 - genetics | Population Surveillance | Cancer patients | Research | Gene mutations | Health aspects | Colorectal cancer | Index Medicus | Abridged Index Medicus
Journal Article
Journal of medical genetics, ISSN 0022-2593, 2010, Volume 47, Issue 3, pp. 169 - 175
Journal Article
Acta Paediatrica, International Journal of Paediatrics, ISSN 0803-5253, 11/2017, Volume 106, Issue 11, pp. 1875 - 1881
Journal Article
Gut, ISSN 0017-5749, 07/2018, Volume 67, Issue 7, pp. 1306 - 1316
Journal Article
by Antoniou, Antonis C and Wang, Xianshu and Fredericksen, Zachary S and McGuffog, Lesley and Tarrell, Robert and Sinilnikova, Olga M and Healey, Sue and Morrison, Jonathan and Kartsonaki, Christiana and Lesnick, Timothy and Ghoussaini, Maya and Barrowdale, Daniel and Peock, Susan and Cook, Margaret and Oliver, Clare and Frost, Debra and Eccles, Diana and Evans, D. Gareth and Eeles, Ros and Izatt, Louise and Chu, Carol and Douglas, Fiona and Paterson, Joan and Stoppa-Lyonnet, Dominique and Houdayer, Claude and Mazoyer, Sylvie and Giraud, Sophie and Lasset, Christine and Remenieras, Auey and Caron, Olivier and Hardouin, Agnès and Berthet, Pascaline and Hogervorst, Frans B. L and Rookus, Matti A and Jager, Agnes and van den Ouweland, Ans and Hoogerbrugge, Nicoline and van der Luijt, Rob B and Meijers-Heijboer, Hanne and Gómez García, Encarna B and Devilee, Peter and Vreeswijk, Maaike P. G and Lubinski, Jan and Jakubowska, Anna and Gronwald, Jacek and Huzarski, Tomasz and Byrski, Tomasz and Górski, Bohdan and Cybulski, Cezary and Spurdle, Amanda B and Holland, Helene and Goldgar, David E and John, Esther M and Hopper, John L and Southey, Melissa and Buys, Sauna S and Daly, Mary B and Terry, Mary-Beth and Schmutzler, Rita K and Wappenschmidt, Barbara and Engel, Christoph and Meindl, Alfons and Preisler-Adams, Sabine and Arnold, Norbert and Niederacher, Dieter and Sutter, Christian and Domchek, Susan M and Nathanson, Katherine L and Rebbeck, Timothy and Blum, Joanne L and Piedmonte, Marion and Roiguez, Gustavo C and Wakeley, Katie and Boggess, John F and Basil, Jack and Blank, Stephanie V and Friedman, Eitan and Kaufman, Bella and Laitman, Yael and Milgrom, Roni and Anulis, Irene L and Glendon, Gord and Ozcelik, Hilmi and Kirchhoff, Tomas and Vijai, Joseph and Gaudet, Mia M and Altshuler, David and Guiducci, Candace and Loman, Niklas and Harbst, Katja and Rantala, Johanna and Ehrencrona, Hans and Gerdes, Anne-Marie and Thomassen, Mads and Sunde, Lone and Peterlongo, Paolo and Manoukian, Siranoush and Bonanni, Bernardo and Viel, Alessana and Radice, Paolo and ... and KConFab and EMBRACE and GEMO Study Collaborators and GENICA and MOD SQUAD and HEBON and SWE-BRCA and kConFab and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature genetics, ISSN 1061-4036, 2010, Volume 42, Issue 10, pp. 885 - 892
Journal Article
Biology of reproduction, 06/2019
Nucleotide-binding oligomerization domain (NOD)-like receptors with a pyrin domain (PYD), NLRPs, are pattern-recognition receptors, well recognized for their... 
Journal Article
Gut, ISSN 0017-5749, 09/2017, Volume 66, Issue 9, pp. 1657 - 1664
Journal Article
Genetics, ISSN 0016-6731, 2017, Volume 207, Issue 1, pp. 215 - 228
Renal agenesis (RA) is one of the more extreme examples of congenital anomalies of the kidney and urinary tract (CAKUT). Bilateral renal agenesis is almost... 
GREB1L | CAKUT | Renal agenesis | Whole exome sequencing | Retinoic acid | URETERAL BUD | renal agenesis | BRANCHING MORPHOGENESIS | ZEBRAFISH KIDNEY DEVELOPMENT | CONGENITAL-ANOMALIES | whole exome sequencing | CANCER GROWTH | BREAST-CANCER | retinoic acid | HUMAN GENOME | URINARY-TRACT | GENETICS & HEREDITY | COPY NUMBER VARIATION | TRANSCRIPTION FACTOR | Chromatin | Syngeneic grafts | Congenital defects | Genes | Retinoic acid receptors | Estrogen | Thyroid gland | Urinary tract | Defects | Morphogenesis | Genotype & phenotype | Receptors | Rodents | Urogenital system | CRISPR | Congenital diseases | Zebrafish | Births | Heredity | Gene expression | Acids | Mutagenesis | Congenital anomalies | Stem cells | Mutation | Kidney diseases | Anomalies | Loss of Function Mutation | Kidney - embryology | Kidney - pathology | Humans | Male | Neoplasm Proteins - metabolism | Kidney Diseases - genetics | Receptors, Retinoic Acid - genetics | Exome | Kidney - metabolism | Congenital Abnormalities - genetics | Female | Neoplasm Proteins - genetics | Kidney Diseases - congenital | Kidney Diseases - pathology | Zebrafish Proteins - metabolism | Receptors, Retinoic Acid - metabolism | Congenital Abnormalities - pathology | Proteins - genetics | Animals | Proteins - metabolism | Kidney - abnormalities | Pedigree | Mice | Zebrafish Proteins - genetics | Usage | Research | Genetic variation | Exome sequencing | Index Medicus
Journal Article