The Cowden syndrome: a clinical and genetic study in 21 patients

Th. M. Starink, J.P.W. van der Veen, F. Arwert, +3

Clinical Genetics

Somatic mosaicism in Fanconi anemia: molecular basis and clinical significance.

Jerome R. Lo Ten Foe, M. L. Kwee, Martin A. Rooimans, +13

PubMed

Somatic Mosaicism in Fanconi Anemia: Molecular Basis and Clinical Significance

Jerome R. Lo Ten Foe, M. L. Kwee, Martin A. Rooimans, +13

European Journal of Human Genetics

Rapidly progressive autosomal dominant parkinsonism and dementia with pallido‐ponto‐nigral degeneration

Ronald F. Pfeiffer, Mohit Bhatt, Robert L. Schelper, +6

Annals of Neurology

Classification of Fanconi anemia patients by complementation analysis: evidence for a fifth genetic subtype

Hans Joenje, JR Lo ten Foe, AB Oostra, +6

Blood

Integrated human papillomavirus type 16 and loss of heterozygosity at 11q22 and 18q21 in an oral carcinoma and its derivative cell line.

Renske D.M. Steenbergen, Mario Hermsen, Jan M.M. Walboomers, +4

PubMed

PathologyTumor BiologyCarcinomaOral CancerCancer-associated Virus +18

Inherited Susceptibility to Bleomycin-Induced Chromatid Breaks in Cultured Peripheral Blood Lymphocytes

Jacqueline Cloos, Eline J. C. Nieuwenhuis, Dorret I. Boomsma, +5

JNCI Journal of the National Cancer Institute

Localization of the Gene for Rapidly Progressive Autosomal Dominant Parkinsonism and Dementia with Pallido-Ponto-Nigral Degeneration to Chromosome 17q21

Mario Wijker, Eric C. Wolters, Martin A. Rooimans, +6

Human Molecular Genetics

Neurodegenerative DiseasesProgressive ParkinsonismAlzheimer's DiseasePallido-ponto-nigral DegenerationGenetic Disorder +13

Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene

Mario Wijker, Sarah Herterich, CGM van Berkel, +24

European Journal of Human Genetics

BiologyGenetic AnalysisHeterogeneous SpectrumAllelic VariantGenetic Disorder +8

Mutations induced by X-rays at the HPRT locus in cultured Chinese hamster cells are mostly large deletions

Harry Vrieling, J.W.I.M. Simons, F. Arwert, +2

Mutation Research Letters

Hprt LocusGenome InstabilityXenotransplantationCytogeneticsGenetics +6