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Germline variants in POLE are associated with early onset mismatch repair deficient colorectal cancer. [electronic resource] by
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- Wijnen, Juul T
- Tops, Carli M
- Ligtenberg, Marjolijn J
- Vasen, Hans F A
- Hes, Frederik J
- Morreau, Hans
- van Wezel, Tom
Producer: 20160428
In:
European journal of human genetics : EJHG vol. 23
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62.
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Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policy. [electronic resource] by
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- Vasen, Hans F A
- Vos, Yvonne J
- van Wezel, Tom
- Tops, Carli M
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Producer: 20210202
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European journal of human genetics : EJHG vol. 28
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Paraganglioma and pheochromocytoma upon maternal transmission of SDHD mutations. [electronic resource] by
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- Corssmit, Eleonora P M
- Dinjens, Winand N M
- de Krijger, Ronald R
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Producer: 20141104
In:
BMC medical genetics vol. 15
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Early onset MSI-H colon cancer with MLH1 promoter methylation, is there a genetic predisposition? [electronic resource] by
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- de Meijer, Emile J
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- van Engeland, Manon
- Oosting, Jan
- Hes, Frederik J
- Tops, Carli M J
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- Morreau, Hans
Producer: 20100816
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65.
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Low penetrance of a SDHB mutation in a large Dutch paraganglioma family. [electronic resource] by
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- Morreau, Hans
- Romijn, Johannes A
- Jansen, Jeroen C
- Vriends, Annette H J T
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Producer: 20100713
In:
BMC medical genetics vol. 11
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66.
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Parent-of-origin tumourigenesis is mediated by an essential imprinted modifier in SDHD-linked paragangliomas: SLC22A18 and CDKN1C are candidate tumour modifiers. [electronic resource] by
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- Jansen, Jeroen C
- Corssmit, Eleonora P M
- Corver, Willem E
- Morreau, Hans
- Bovée, Judith V M G
- Bayley, Jean-Pierre
- Devilee, Peter
Producer: 20170823
In:
Human molecular genetics vol. 25
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67.
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MUTYH gene variants and breast cancer in a Dutch case–control study. [electronic resource] by
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- Nielsen, Maartje
- Seynaeve, Caroline
- Wijnen, Juul T
- Breuning, Martijn H
- van Asperen, Christi J
- Schutte, Mieke
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Producer: 20121119
In:
Breast cancer research and treatment vol. 134
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68.
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Distinct Patterns of Somatic Mosaicism in the APC Gene in Neoplasms From Patients With Unexplained Adenomatous Polyposis. [electronic resource] by
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- Nielsen, Maartje
- Tops, Carli M J
- Wijnen, Juul T
- Hes, Frederik J
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Producer: 20170605
In:
Gastroenterology vol. 152
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69.
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High-resolution melting (HRM) re-analysis of a polyposis patients cohort reveals previously undetected heterozygous and mosaic APC gene mutations. [electronic resource] by
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- Voorendt, Marsha
- Vossen, Rolf H A M
- Nielsen, Maartje
- Vasen, Hans F A
- Morreau, Hans
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Producer: 20160308
In:
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70.
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MUTYH and the mismatch repair system: partners in crime? [electronic resource] by
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- Ligtenberg, Marjolijn J
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- Weiss, Marjan M
- Tops, Carli M J
- Hes, Frederik J
- de Bock, Geertruida H
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Producer: 20070402
In:
Human genetics vol. 119
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71.
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Pancreatic cancer-associated gene polymorphisms in a nation-wide cohort of p16-Leiden germline mutation carriers; a case-control study. [electronic resource] by
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- Ausems, Margreet G
- Dommering, Charlotte J
- van der Kolk, Lizet E
- Maiburg, Merel C
- Spruijt, Liesbeth
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Producer: 20160218
In:
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High Growth Rate of Pancreatic Ductal Adenocarcinoma in [electronic resource] by
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- Veenendaal, Roeland A
- Putter, Hein
- Feshtali, Shirin
- van Mil, Anneke M
- Gruis, Nelleke A
- Tollenaar, Rob A
- Bergman, Wilma
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Producer: 20190927
In:
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Deep sequencing to reveal new variants in pooled DNA samples. [electronic resource] by
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- Weigel, Detlef
- van Galen, Michiel
- Taschner, Peter E M
- Tops, Carli M J
- Breuning, Martijn H
- van Ommen, Gert-Jan B
- den Dunnen, Johan T
- Devilee, Peter
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Producer: 20100203
In:
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74.
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CDC73-Related Disorders: Clinical Manifestations and Case Detection in Primary Hyperparathyroidism. [electronic resource] by
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- Hamdy, Neveen A T
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- Menko, Fred H
- van Nesselrooij, Bernadette P M
- Netea-Maier, Romana T
- Oosterwijk, Jan C
- Valk, Gerlof D
- Wolffenbuttel, Bruce H R
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Producer: 20171214
In:
The Journal of clinical endocrinology and metabolism vol. 102
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Cancer risk and genotype-phenotype correlations in PTEN hamartoma tumor syndrome. [electronic resource] by
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- Evans, D Gareth
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- Hes, Frederik J
- Hodgson, Shirley V
- Olderode-Berends, Maran J W
- Aretz, Stefan
- Heinimann, Karl
- Gómez García, Encarna B
- Douglas, Fiona
- Spigelman, Allan
- Timshel, Susanne
- Lindor, Noralane M
- Vasen, Hans F A
Producer: 20150511
In:
Familial cancer vol. 13
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76.
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Molecular Background of Colorectal Tumors From Patients With Lynch Syndrome Associated With Germline Variants in PMS2. [electronic resource] by
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- Hes, Frederik J
- van Hest, Liselot P
- Letteboer, Tom G W
- Olderode-Berends, Maran J W
- Ruano, Dina
- Spruijt, Liesbeth
- Suerink, Manon
- Tops, Carli M
- van Eijk, Ronald
- Morreau, Hans
- van Wezel, Tom
- Nielsen, Maartje
Producer: 20180914
In:
Gastroenterology vol. 155
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77.
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Colorectal cancer risk variants on 11q23 and 15q13 are associated with unexplained adenomatous polyposis. [electronic resource] by
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- Tops, Carli M
- Schrumpf, Melanie
- Nielsen, Maartje
- Huijts, Petra E A
- Wijnen, Juul T
- Wagner, Anja
- Gómez García, Encarna B
- Sijmons, Rolf H
- Menko, Fred H
- Letteboer, Tom G W
- Hoogerbrugge, Nicoline
- Harryvan, Jan
- Kampman, Ellen
- Morreau, Hans
- Vasen, Hans F A
- van Wezel, Tom
Producer: 20140808
In:
Journal of medical genetics vol. 51
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78.
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Loss of maternal chromosome 11 is a signature event in SDHAF2, SDHD, and VHL-related paragangliomas, but less significant in SDHB-related paragangliomas. [electronic resource] by
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- Hensen, Erik F
- Jordanova, Ekaterina S
- Korpershoek, Esther
- van der Horst-Schrivers, Anouk Na
- Cornelisse, Cees
- Corssmit, Eleonora P M
- Hes, Frederik J
- Jansen, Jeroen C
- Kunst, Henricus P M
- Timmers, Henri J L M
- Bateman, Adrian
- Eccles, Diana
- Bovée, Judith V M G
- Devilee, Peter
- Bayley, Jean-Pierre
Producer: 20171009
In:
Oncotarget vol. 8
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Accuracy of Hereditary Diffuse Gastric Cancer Testing Criteria and Outcomes in Patients With a Germline Mutation in CDH1. [electronic resource] by
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- Vogelaar, Ingrid P
- Manders, Peggy
- van der Kolk, Lizet E
- Cats, Annemieke
- van Hest, Liselotte P
- Sijmons, Rolf
- Aalfs, Cora M
- Ausems, Margreet G E M
- Gómez García, Encarna B
- Wagner, Anja
- Hes, Frederik J
- Arts, Neeltje
- Mensenkamp, Arjen R
- van Krieken, J Han
- Hoogerbrugge, Nicoline
- Ligtenberg, Marjolijn J L
Producer: 20151229
In:
Gastroenterology vol. 149
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80.
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Compliance with periodic surveillance for Von-Hippel-Lindau disease. [electronic resource] by
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- Aaronson, Neil K
- Hes, Frederik J
- Links, Thera P
- Zonnenberg, Bernard A
- Lenders, Jacques W M
- Majoor-Krakauer, Danielle
- Van Os, Theo A M
- Gomez-Garcia, Encarna B
- de Herder, Wouter
- van der Luijt, Rob B
- van den Ouweland, Ans M W
- Van Hest, Liselot P
- Verhoef, Senno
- Bleiker, Eveline M A
Producer: 20110928
In:
Genetics in medicine : official journal of the American College of Medical Genetics vol. 13
Availability: No items available.
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