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Journal of Medical Genetics|June 5, 2010
Investigation of the Birt-Hogg-Dube tumour suppressor gene (FLCN) in familial and sporadic colorectal cancerMichael S Nahorski, Derek H K Lim, Lynn Martin, et al.Human Mutation|October 6, 2009
A new locus-specific database (LSDB) for mutations in the folliculin (FLCN) geneDerek H K Lim, Pauline K Rehal, Michael S Nahorski, et al.BMC Pediatrics|July 5, 2014
Spontaneous pneumothorax as indicator for Birt-Hogg-Dubé syndrome in paediatric patientsPaul C Johannesma, Ben E E M van den Borne, Johannes J P Gille, et al.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.The Journal of Chemical Physics|August 24, 2015
The atomic structure of low-index surfaces of the intermetallic compound InPdG M McGuirk, J Ledieu, É Gaudry, 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.Pageof 14