Mark M. Entius

发表

Molecular and phenotypic markers of hamartomatous polyposis syndromes in the gastrointestinal tract.

S. Hamilton, M. V. van Velthuysen, J. Wilson, 1999, Hepato-gastroenterology.

Pathogenesis of Adenocarcinoma in Peutz-Jeghers Syndrome1

Jeffrey, Stanley, B. Vogelstein, 2006 .

Novel mutations in the LKB1/STK11 gene in Dutch Peutz‐Jeghers families

J. Lubiński, D. Lindhout, F. D. de Rooij, 1999, Human mutation.

Plakophilin-2 Mutations Are the Major Determinant of Familial Arrhythmogenic Right Ventricular Dysplasia/Cardiomyopathy

R. Hauer, I. V. Van Gelder, A. Wilde, 2006, Circulation.

Cancer risk in Peutz‐Jeghers syndrome

D. Lindhout, J. Wilson, G. Offerhaus, 1998 .

Mutation screening of EXT1 and EXT2 by denaturing high-performance liquid chromatography, direct sequencing analysis, fluorescence in situ hybridization, and a new multiplex ligation-dependent probe amplification probe set in patients with multiple osteochondromas.

L. Sangiorgi, W. Wuyts, Mark M. Entius, 2008, The Journal of molecular diagnostics : JMD.

MLPA diagnostics of complex microbial communities: relative quantification of bacterial species in oral biofilms.

W. Crielaard, R. V. van Spanning, J. T. ten Cate, 2008, Journal of microbiological methods.

Pathogenesis of adenocarcinoma in Peutz-Jeghers syndrome.

M. Polymeropoulos, J. Trent, B. Vogelstein, 1998, Cancer research.

Advances in Brief Pathogenesis of Adenocarcinoma in Peutz-Jeghers Syndrome 1

Jeffrey, Stephen, Stanley, 2006 .

Peutz-Jeghers syndrome: 78-year follow-up of the original family

P. Boor, A. M. Westerman, Mark M. Entius, 1999, The Lancet.

Germline and somatic mutations of the STK11/LKB1 Peutz-Jeghers gene in pancreatic and biliary cancers.

R. Hruban, M. Goggins, S. Kern, 1999, The American journal of pathology.

Molecular genetic alterations in hamartomatous polyps and carcinomas of patients with Peutz-Jeghers syndrome

J. Keller, M. V. van Velthuysen, F. Giardiello, 2001, Journal of clinical pathology.

Peutz-Jeghers polyps, dysplasia, and K-ras codon 12 mutations

R. Slebos, M. V. van Velthuysen, J. Wilson, 1997, Gut.

Microsatellite instability and expression of hMLH-1 and hMSH-2 in sebaceous gland carcinomas as markers for Muir-Torre syndrome.

J. Keller, F. Giardiello, G. Offerhaus, 2000, Clinical cancer research : an official journal of the American Association for Cancer Research.

Upper gastrointestinal polyps in familial adenomatous polyposis.

G. Offerhaus, Mark M. Entius, F. Giardiello, 1999, Hepato-gastroenterology.

High proportion of large genomic deletions and a genotype–phenotype update in 80 unrelated families with juvenile polyposis syndrome

R. Siebert, M. Stolte, L. Sunde, 2007, Journal of Medical Genetics.

Inflammatory Gene Haplotype-Interaction Networks Involved in Coronary Collateral Formation

F. Liang, D. Grobbee, Y. van der Graaf, 2008, Human Heredity.

Multiple hyperplastic polyps in the stomach: evidence for clonality and neoplastic potential.

R. Slebos, G. Offerhaus, Mark M. Entius, 1997, Gastroenterology.

Microsatellite Instability and Expression of hMLH-1 and hMSH-2 in Sebaceous Gland Carcinomas as Markers for Muir-Torre Syndrome 1

J. Keller, F. Giardiello, G. Offerhaus, 2000 .

Molecular genetic alterations in gastrointestinal polyposis syndromes: with emphasis on the Peutz-Jeghers syndrome

G. Offerhaus, Mark M. Entius, F. Giardiello, 2000 .

Molecular genetic alterations in gastrointestinal polyposis syndromes : with emphasis on the Peutz-Jeghers syndrome

K. Kinzler, U. Mujumdar, F. Giardiello, 2009 .

UvA-DARE (Digital Academic Repository) Molecular genetic alterations in gastrointestinal polyposis syndromes: with emphasis on the Peutz-Jeghers syndrome

F. Giardiello, Mark M. Entius, P. Drillenburg, 2009 .