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Results: 1-11 |
Results: 11

Authors: WIJNEN J VANDERKLIFT H VASEN H KHAN PM MENKO F TOPS C HEIJBOER HM LINDHOUT D MOLLER P FODDE R
Citation: J. Wijnen et al., MSH2 GENOMIC DELETIONS ARE A FREQUENT CAUSE OF HNPCC, Nature genetics, 20(4), 1998, pp. 326-328

Authors: PELTOMAKI P VASEN HFA BISGAARD ML BUERSTEDDE JM FRIEDL W GRANDJOUAN S HUTTER P KOHONENCORISH M KOLODNER R KURZAWSKI G LINDBLOM A LYNCH HT PIEPOLI A DELEON MP RADICE P THIBODEAU S WEBER W WEST S WIJNEN J
Citation: P. Peltomaki et al., MUTATIONS PREDISPOSING TO HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER -DATABASE AND RESULTS OF A COLLABORATIVE STUDY, Gastroenterology, 113(4), 1997, pp. 1146-1158

Authors: ROGAN PK SCHNEIDER TD FAUX B WIJNEN J RADICE P BABA S SCOTT R VIEL A GENUARDI M KHAN PM FODDE R
Citation: Pk. Rogan et al., INFORMATION THEORY-BASED ANALYSIS OF SPLICE JUNCTION MUTATIONS IN HEREDITARY NONPOLYPOSIS COLON-CANCER (HNPCC), American journal of human genetics, 61(4), 1997, pp. 438-438

Authors: WIJNEN J KHAN PM VASEN H VANDERKLIFT H MULDER A VANLEEUWENCORNELISSE I BAKKER B LOSEKOOT M MOLLER P FODDE R
Citation: J. Wijnen et al., HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER FAMILIES NOT COMPLYING WITHTHE AMSTERDAM CRITERIA SHOW EXTREMELY-LOW-FREQUENCY OF MISMATCH-REPAIR-GENE MUTATIONS, American journal of human genetics, 61(2), 1997, pp. 329-335

Authors: BALA S KRAUS C WIJNEN J KHAN PM BALLHAUSEN WG
Citation: S. Bala et al., MULTIPLE PRODUCTS IN THE PROTEIN TRUNCATION TEST DUE TO ALTERNATIVE SPLICING IN THE ADENOMATOUS POLYPOSIS-COLI (APC) GENE, Human genetics, 98(5), 1996, pp. 528-533

Authors: WIJNEN J
Citation: J. Wijnen, IS ROBERTSON,PAT AN ANTI-SEMITE, Commentary, 101(1), 1996, pp. 11-11

Authors: KOHONENCORISH M ROSS VL DOE WF KOOL DA EDKINS E FARAGHER I WIJNEN J KHAN PM MACRAE F STJOHN DJB
Citation: M. Kohonencorish et al., RNA-BASED MUTATION SCREENING IN HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER, American journal of human genetics, 59(4), 1996, pp. 818-824

Authors: WIJNEN J KHAN PM VASEN H MENKO F VANDERKLIFT H VANDENBROEK M VANLEEUWENCORNELISSE I NAGENGAST F MEIJERSHEIJBOER EJ LINDHOUT D GRIFFIOEN G CATS A KLEIBEUKER J VARESCO L BERTARIO L BISGAARD ML MOHR J KOLODNER R FODDE R
Citation: J. Wijnen et al., MAJORITY OF HMLH1 MUTATIONS RESPONSIBLE FOR HEREDITARY NONPOLYPOSIS COLORECTAL-CANCER CLUSTER AT THE EXONIC REGION 15-16, American journal of human genetics, 58(2), 1996, pp. 300-307

Authors: WIJNEN J VASEN H KHAN PM MENKO FH VANDERKLIFT H VANLEEUWEN C VANDENBROEK M VANLEEUWENCORNELISSE I NAGENGAST F MEIJERSHEIJBOER A LINDHOUT D GRIFFIOEN G CATS A KLEIBEUKER J VARESCO L BERTARIO L BISGAARD ML MOHR J FODDE R
Citation: J. Wijnen et al., 7 NEW MUTATIONS IN HMSH2, AN HNPCC GENE, IDENTIFIED BY DENATURING GRADIENT-GEL ELECTROPHORESIS, American journal of human genetics, 56(5), 1995, pp. 1060-1066

Authors: WIJNEN J FODDE R KHAN PM
Citation: J. Wijnen et al., DGGE POLYMORPHISM IN INTRON-10 OF MSH2, THE HNPCC GENE, Human molecular genetics, 3(12), 1994, pp. 2268-2268

Authors: RENAULT B VANDENBROEK M FODDE R WIJNEN J PELLEGATA NS AMADORI D KHAN PM RANZANI GN
Citation: B. Renault et al., BASE TRANSITIONS ARE THE MOST FREQUENT GENETIC CHANGES AT P53 IN GASTRIC-CANCER, Cancer research, 53(11), 1993, pp. 2614-2617
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