AAAAAA

   
Results: 1-20 |
Results: 20
INTERACTIONS BETWEEN HAMARTIN AND TUBERIN, THE TSC1 AND TSC2 GENE-PRODUCTS
Authors: VANSLEGTENHORST M NELLIST M CHEADLE J NAGELKERKEN B REUSER A VANDENOUWELAND A SAMPSON J VANDERSLUIJS P HALLEY D
Citation: M. Vanslegtenhorst et al., INTERACTIONS BETWEEN HAMARTIN AND TUBERIN, THE TSC1 AND TSC2 GENE-PRODUCTS, European journal of human genetics, 6, 1998, pp. 601-601
DNA DIAGNOSIS OF CZECH TUBEROUS SCLEROSIS PATIENTS
Authors: VRTEL R SANTAVY J SANTAVA A POLAK P KREJCIRIKOVA E TEMPELAARS A VANDENOUWELAND A HALLEY D
Citation: R. Vrtel et al., DNA DIAGNOSIS OF CZECH TUBEROUS SCLEROSIS PATIENTS, European journal of human genetics, 6, 1998, pp. 4018-4018
INTERACTION BETWEEN HAMARTIN AND TUBERIN, THE TSC1 AND TSC2 GENE-PRODUCTS
Authors: VANSLEGTENHORST M NELLIST M NAGELKERKEN B CHEADLE J SNELL R VANDENOUWELAND A REUSER A SAMPSON J HALLEY D VANDERSLUIJS P
Citation: M. Vanslegtenhorst et al., INTERACTION BETWEEN HAMARTIN AND TUBERIN, THE TSC1 AND TSC2 GENE-PRODUCTS, Human molecular genetics, 7(6), 1998, pp. 1053-1057
MUTATIONS IN THE BRCA1 AND BRCA2 GENES - UPTAKE OF PRESYMPTOMATIC DNATEST, PREVENTIVE CHOICES AND BREAST-CANCER RISK AFTER PROPHYLACTIC MASTECTOMY
Authors: MEIJERSHEIJBOER H VERHOOG L BREKELMANS C VANGEEL B SEYNAEVE C WAGNER A VANDENOUWELAND A FRETS P NIERMEIJER M KLIJN J
Citation: H. Meijersheijboer et al., MUTATIONS IN THE BRCA1 AND BRCA2 GENES - UPTAKE OF PRESYMPTOMATIC DNATEST, PREVENTIVE CHOICES AND BREAST-CANCER RISK AFTER PROPHYLACTIC MASTECTOMY, European journal of cancer, 34, 1998, pp. 95-95
SURVIVAL AND TUMOR CHARACTERISTICS OF BREAST-CANCER PATIENTS WITH GERMLINE MUTATIONS OF BRCA1
Authors: VERHOOG LC BREKELMANS CTM SEYNAEVE C VANDENBOSCH LMC DAHMEN G VANGEEL AN TILANUSLINTHORST MMA BARTELS CCM WAGNER A VANDENOUWELAND A DEVILEE P MEIJERSHEIJBOER EJ KLIJN JGM
Citation: Lc. Verhoog et al., SURVIVAL AND TUMOR CHARACTERISTICS OF BREAST-CANCER PATIENTS WITH GERMLINE MUTATIONS OF BRCA1, Lancet, 351(9099), 1998, pp. 316-321
COMMON C-TO-T SUBSTITUTION AT POSITION--480 OF THE HEPATIC LIPASE PROMOTER ASSOCIATED WITH A LOWERED LIPASE ACTIVITY IN CORONARY-ARTERY DISEASE PATIENTS
Authors: JANSEN H VERHOEVEN AJM WEEKS L KASTELEIN JJP HALLEY DJJ VANDENOUWELAND A JUKEMA JW SEIDELL JC BIRKENHAGER JC
Citation: H. Jansen et al., COMMON C-TO-T SUBSTITUTION AT POSITION--480 OF THE HEPATIC LIPASE PROMOTER ASSOCIATED WITH A LOWERED LIPASE ACTIVITY IN CORONARY-ARTERY DISEASE PATIENTS, Arteriosclerosis, thrombosis, and vascular biology, 17(11), 1997, pp. 2837-2842
QUALITY GUIDELINES AND STANDARDS FOR GENETIC LABORATORIES CLINICS IN PRENATAL-DIAGNOSIS ON FETAL SAMPLES OBTAINED BY INVASIVE PROCEDURES - AN ATTEMPT TO ESTABLISH A COMMON EUROPEAN FRAMEWORK FOR QUALITY ASSESSMENT/
Authors: KROISEL PM FRYNS JP MATTHIJS G BRONDUMNIELSEN K VEJERSLEV L VONKOSKULL H GIRAUDON E SAURA R HELD K MULLERREIBLE CR METAXOTOU C GENUARDI M PIOMBO G SCHNEIDER F SMEETS D VANDENOUWELAND A PACHECO P CORREIA H BINKERT F GABARRON J GALLANO P KRISTOFFERSSON U ANVRET M HOWELL R STENHOUSE S
Citation: Pm. Kroisel et al., QUALITY GUIDELINES AND STANDARDS FOR GENETIC LABORATORIES CLINICS IN PRENATAL-DIAGNOSIS ON FETAL SAMPLES OBTAINED BY INVASIVE PROCEDURES - AN ATTEMPT TO ESTABLISH A COMMON EUROPEAN FRAMEWORK FOR QUALITY ASSESSMENT/, European journal of human genetics, 5(6), 1997, pp. 342-350
RAPID ANTIBODY-TEST FOR DIAGNOSING FRAGILE-X-SYNDROME - A VALIDATION OF THE TECHNIQUE
Authors: WILLEMSEN R SMITS A MOHKAMSING S VANBEERENDONK H DEHAAN A DEVRIES B VANDENOUWELAND A SISTERMANS E GALJAARD H OOSTRA BA
Citation: R. Willemsen et al., RAPID ANTIBODY-TEST FOR DIAGNOSING FRAGILE-X-SYNDROME - A VALIDATION OF THE TECHNIQUE, Human genetics, 99(3), 1997, pp. 308-311
IDENTIFICATION OF THE TUBEROUS SCLEROSIS GENE TSC1 ON CHROMOSOME 9Q34
Authors: VANSLEGTENHORST M DEHOOGT R HERMANS C NELLIST M JANSSEN B VERHOEF S LINDHOUT D VANDENOUWELAND A HALLEY D YOUNG J BURLEY M JEREMIAH S WOODWARD K NAHMIAS J FOX M EKONG R OSBORNE J WOLFE J POVEY S SNELL RG CHEADLE JP JONES AC TACHATAKI M RAVINE D SAMPSON JR REEVE MP RICHARDSON P WILMER F MUNRO C HAWKINS TL SEPP T ALI JBM WARD S GREEN AJ YATES JRW KWIATKOWSKA J HENSKE EP SHORT MP HAINES JH JOZWIAK S KWIATKOWSKI DJ
Citation: M. Vanslegtenhorst et al., IDENTIFICATION OF THE TUBEROUS SCLEROSIS GENE TSC1 ON CHROMOSOME 9Q34, Science, 277(5327), 1997, pp. 805-808
RAPID ANTIBODY-TEST FOR PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME ON AMNIOTIC-FLUID CELLS - A NEW APPRAISAL
Authors: WILLEMSEN R LOS F MOHKAMSING S VANDENOUWELAND A DEELEN W GALJAARD H OOSTRA B
Citation: R. Willemsen et al., RAPID ANTIBODY-TEST FOR PRENATAL-DIAGNOSIS OF FRAGILE-X-SYNDROME ON AMNIOTIC-FLUID CELLS - A NEW APPRAISAL, Journal of Medical Genetics, 34(3), 1997, pp. 250-251
HEPATIC LIPASE PROMOTER POLYMORPHISM (C-480T) ABOLISHES INSULIN-SENSITIVITY OF HEPATIC LIPASE EXPRESSION
Authors: JANSEN H VERHOEVEN AJM VANDENOUWELAND A JUKEMA W SEIDELL JC
Citation: H. Jansen et al., HEPATIC LIPASE PROMOTER POLYMORPHISM (C-480T) ABOLISHES INSULIN-SENSITIVITY OF HEPATIC LIPASE EXPRESSION, Atherosclerosis, 134(1-2), 1997, pp. 25-25
IDENTIFICATION OF THE TUBEROUS SCLEROSIS GENE (TSC1) ON CHROMOSOME 9Q34
Authors: KWIATKOWSKI DJ HENSKE EP KWIATKOWSKA J YOUNG J BURLEY M JEREMIAH S WOODWARD K NAHMIAS J FOX M EKONG R WOLFE J POVEY S OSBORNE J SNELL RG CHEADLE JP JONES AC TACHATAKI M RAVINE D SAMPSON JR REEVE MP RICHARDSON P WILMER F MUNRO C HAWKINS TL SEPP T ALI JBM WARD S GREEN AJ YATES JRW SHORT MP HAINES JH JOZWIAK S VANSLEGTENHORST M DEHOOGT R HERMANS C NELLIST M JANSSEN B VERHOEF S LINDHOUT D VANDENOUWELAND A HALLEY D
Citation: Dj. Kwiatkowski et al., IDENTIFICATION OF THE TUBEROUS SCLEROSIS GENE (TSC1) ON CHROMOSOME 9Q34, American journal of human genetics, 61(4), 1997, pp. 7-7
UPTAKE PRESYMPTOMATIC DNA TEST AND PREVENTIVE MEASURES IN FAMILIES WITH INHERITED BREAST-CANCER AND OR OVARIAN-CANCER/
Authors: MEIJERSHEIJBOER EJ VANGEEL AN SEYNAEVE C LOGMANS A BARTELS C TILANUSLINTHORST M HALLEY DJJ VANDENOUWELAND A WAGNER A MAJOORKRAKAUER D NIERMEYER MF DEVILEE P KLIJN JGM
Citation: Ej. Meijersheijboer et al., UPTAKE PRESYMPTOMATIC DNA TEST AND PREVENTIVE MEASURES IN FAMILIES WITH INHERITED BREAST-CANCER AND OR OVARIAN-CANCER/, American journal of human genetics, 61(4), 1997, pp. 403-403
FUNCTIONAL-CHARACTERIZATION OF THE TSC1 GENE
Authors: VANSLEGTENHORST M NELLIST M DEHOOGT R BAKKER R VANDENOUWELAND A VANDERSLUIJS P HALLEY D
Citation: M. Vanslegtenhorst et al., FUNCTIONAL-CHARACTERIZATION OF THE TSC1 GENE, American journal of human genetics, 61(4), 1997, pp. 2239-2239
FAMILIAL TRANSLOCATIONS INVOLVING 15Q11-Q13 CAN GIVE RISE TO INTERSTITIAL DELETIONS CAUSING PRADER-WILLI OR ANGELMAN SYNDROME
Authors: HORSTHEMKE B MAATKIEVIT A SLEEGERS E VANDENOUWELAND A BUITING K LICH C MOLLEVANGER P BEVERSTOCK G GILLESSENKAESBACH G SCHWANITZ G
Citation: B. Horsthemke et al., FAMILIAL TRANSLOCATIONS INVOLVING 15Q11-Q13 CAN GIVE RISE TO INTERSTITIAL DELETIONS CAUSING PRADER-WILLI OR ANGELMAN SYNDROME, Journal of Medical Genetics, 33(10), 1996, pp. 848-851
COSMID CONTIGS FROM THE TUBEROUS SCLEROSIS CANDIDATE REGION ON CHROMOSOME 9Q34
Authors: VANSLEGTENHORST M JANSSEN B NELLIST M RAMLAKHAN S HERMANS C HESSELING A VANDENOUWELAND A KWIATKOWSKI D EUSSEN B SAMPSON J DEJONG P HALLEY D
Citation: M. Vanslegtenhorst et al., COSMID CONTIGS FROM THE TUBEROUS SCLEROSIS CANDIDATE REGION ON CHROMOSOME 9Q34, European journal of human genetics, 3(2), 1995, pp. 78-86
RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME
Authors: WILLEMSEN R MOHKAMSING S DEVRIES B DEVYS D VANDENOUWELAND A MANDEL JL GALJAARD H OOSTRA B
Citation: R. Willemsen et al., RAPID ANTIBODY-TEST FOR FRAGILE-X SYNDROME, Lancet, 345(8958), 1995, pp. 1147-1148
SOMATIC MOSAICISM AND CLINICAL VARIATION IN TUBEROUS SCLEROSIS COMPLEX
Authors: VERHOEF S VRTEL R VANESSEN T BAKKER L SIKKENS E HALLEY D LINDHOUT D VANDENOUWELAND A
Citation: S. Verhoef et al., SOMATIC MOSAICISM AND CLINICAL VARIATION IN TUBEROUS SCLEROSIS COMPLEX, Lancet, 345(8943), 1995, pp. 202-202
STRATEGY FOR RELIABLE PRENATAL DETECTION OF NORMAL-MALE CARRIERS OF THE FRAGILE-X-SYNDROME
Authors: HALLEY D VANDENOUWELAND A DEELEN W VERMA I OOSTRA B
Citation: D. Halley et al., STRATEGY FOR RELIABLE PRENATAL DETECTION OF NORMAL-MALE CARRIERS OF THE FRAGILE-X-SYNDROME, American journal of medical genetics, 51(4), 1994, pp. 471-473
USE OF PROBE PW71 (D15S63) IN DNA DIAGNOSTICS OF PRADER-WILLI-SYNDROME PATIENTS
Authors: VANDENOUWELAND A VANDEREST M TIJMENSEN T WESBYVANSWAAY E HALLEY D
Citation: A. Vandenouweland et al., USE OF PROBE PW71 (D15S63) IN DNA DIAGNOSTICS OF PRADER-WILLI-SYNDROME PATIENTS, American journal of human genetics, 53(3), 1993, pp. 1764-1764
Risultati: 1-20 |