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Comprehensive Mutation Analysis of PMS2 in a Large Cohort of Probands Suspected of Lynch Syndrome or Constitutional Mismatch Repair Deficiency (CMMRD) Syndrome
Authors :
Genetica Sectie Oncogenetica Child Health van der Klift, Heleen M Mensenkamp, Arjen R Drost, Mark Bik, Elsa C Vos, Yvonne J Gille, Hans J J P Redeker, Bert E J W Tiersma, Yvonne Zonneveld, José B M García, Encarna Gómez Letteboer, Tom G W Olderode-Berends, Maran J W van Hest, Liselotte P van Os, Theo A Verhoef, Senno Wagner, Anja van Asperen, Christi J Ten Broeke, Sanne W Hes, Frederik J de Wind, Niels Nielsen, Maartje Devilee, Peter Ligtenberg, Marjolijn J L Wijnen, Juul T Tops, Carli M J Genetica Sectie Oncogenetica Child Health van der Klift, Heleen M Mensenkamp, Arjen R Drost, Mark Bik, Elsa C Vos, Yvonne J Gille, Hans J J P Redeker, Bert E J W Tiersma, Yvonne Zonneveld, José B M García, Encarna Gómez Letteboer, Tom G W Olderode-Berends, Maran J W van Hest, Liselotte P van Os, Theo A Verhoef, Senno Wagner, Anja van Asperen, Christi J Ten Broeke, Sanne W Hes, Frederik J de Wind, Niels Nielsen, Maartje Devilee, Peter Ligtenberg, Marjolijn J L Wijnen, Juul T Tops, Carli M J
Publication Year :
2016
Details
Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1395285537
Document Type :
Electronic Resource