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International Journal of Cancer|April 15, 2006
Low prevalence of (pre) malignant lesions in the breast and high prevalence in the ovary and Fallopian tube in women at hereditary high risk of breast and ovarian cancerBrenda B J Hermsen, Paul J van Diest, Johannes Berkhof, et al.Journal of Clinical Pathology|December 25, 2002
Comparative genomic hybridisation divides retinoblastomas into a high and a low level chromosomal instability groupJ E van der Wal, M A J A Hermsen, H J P Gille, et al.Familial Cancer|November 26, 2015
Are lung cysts in renal cell cancer (RCC) patients an indication for FLCN mutation analysis?Paul C Johannesma, Arjan C Houweling, Fred H Menko, et al.European Journal of Haematology|November 9, 2017
Pediatric Diamond-Blackfan anemia in the Netherlands: An overview of clinical characteristics and underlying molecular defectsBirgit van Dooijeweert, C Heleen van Ommen, Frans J Smiers, et al.Journal of Clinical Pathology|September 29, 2005
STRAD in Peutz-Jeghers syndrome and sporadic cancersW W J de Leng, J J Keller, S Luiten, et al.Familial Cancer|July 26, 2012
Heterozygote FANCD2 mutations associated with childhood T Cell ALL and testicular seminomaStephanie Smetsers, Joanne Muter, Claire Bristow, et al.BMC Pulmonary Medicine|August 26, 2022
Birt-Hogg-Dubé syndrome in apparent primary spontaneous pneumothorax patients; results and recommendations for clinical practiceJincey D Sriram, Irma van de Beek, Paul C Johannesma, et al.British Journal of Cancer|October 10, 2002
Genomic deletions of MSH2 and MLH1 in colorectal cancer families detected by a novel mutation detection approachJ J P Gille, F B L Hogervorst, G Pals, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 28, 2018
Newborn blood spot screening for cystic fibrosis with a four-step screening strategy in the NetherlandsJeannette E Dankert-Roelse, Marelle J Bouva, Bernadette S Jakobs, et al.European Journal of Human Genetics : EJHG|September 19, 2019
Declining detection rates for APC and biallelic MUTYH variants in polyposis patients, implications for DNA testing policyDiantha Terlouw, Manon Suerink, Sunny S Singh, et al.Pageof 11