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Results: 1-25 | 26-50 | 51-75
Results: 1-25/75
AUTOSOMAL-DOMINANT CONGENITAL CATARACT ASSOCIATED WITH A MISSENSE MUTATION IN THE HUMAN ALPHA-CRYSTALLIN GENE CRYAA
Authors: LITT M KRAMER P LAMORTICELLA DM MURPHEY W LOVRIEN EW WELEBER RG
Citation: M. Litt et al., AUTOSOMAL-DOMINANT CONGENITAL CATARACT ASSOCIATED WITH A MISSENSE MUTATION IN THE HUMAN ALPHA-CRYSTALLIN GENE CRYAA, Human molecular genetics, 7(3), 1998, pp. 471-474
FURTHER LOCALIZATION OF A GENE FOR PAROXYSMAL DYSTONIC CHOREOATHETOSIS TO A 5-CM REGION ON CHROMOSOME 2Q34
Authors: RASKIND WH BOLIN T WOLFF J FINK J MATSUSHITA M LITT M LIPE H BIRD TD
Citation: Wh. Raskind et al., FURTHER LOCALIZATION OF A GENE FOR PAROXYSMAL DYSTONIC CHOREOATHETOSIS TO A 5-CM REGION ON CHROMOSOME 2Q34, Human genetics, 102(1), 1998, pp. 93-97
MATCHING ALCOHOLISM TREATMENTS TO CLIENT HETEROGENEITY - PROJECT MATCH 3-YEAR DRINKING OUTCOMES
Authors: ALLEN J ANTON RF BABOR TF CARBONARI J CARROLL KM CONNORS GJ COONEY NL DELBOCA FK DICLEMENTE CC DONOVAN D KADDEN RM LITT M LONGABAUGH R MATTSON M MILLER WR RANDALL CL ROUNSAVILLE BJ RYCHTARIK RG STOUT RL TONIGAN JS WIRTZ PW ZWEBEN A
Citation: J. Allen et al., MATCHING ALCOHOLISM TREATMENTS TO CLIENT HETEROGENEITY - PROJECT MATCH 3-YEAR DRINKING OUTCOMES, Alcoholism, clinical and experimental research, 22(6), 1998, pp. 1300-1311
ANALYSIS OF THE ALPHA-SYNUCLEIN G209A MUTATION IN FAMILIAL PARKINSONS-DISEASE
Authors: ZAREPARSI S KAY J CAMICIOLI R KRAMER P NUTT J BIRD T LITT M PAYAMI H
Citation: S. Zareparsi et al., ANALYSIS OF THE ALPHA-SYNUCLEIN G209A MUTATION IN FAMILIAL PARKINSONS-DISEASE, Lancet, 351(9095), 1998, pp. 37-38
CONFIRMATION OF LINKAGE OF CLOUSTON-SYNDROME (HIDROTIC ECTODERMAL DYSPLASIA) TO 13Q11-Q12.1 WITH EVIDENCE FOR MULTIPLE INDEPENDENT MUTATIONS
Authors: TAYLOR TD HAYFLICK SJ MCKINNON W GUTTMACHER AE HOVNANIAN A LITT M ZONANA J
Citation: Td. Taylor et al., CONFIRMATION OF LINKAGE OF CLOUSTON-SYNDROME (HIDROTIC ECTODERMAL DYSPLASIA) TO 13Q11-Q12.1 WITH EVIDENCE FOR MULTIPLE INDEPENDENT MUTATIONS, Journal of investigative dermatology, 111(1), 1998, pp. 83-85
HIGH-PRESSURE ELECTRICAL-CONDUCTIVITY STUDIES OF ACID DOPED POLYBENZIMIDAZOLE
Authors: FONTANELLA JJ WINTERSGILL MC WAINRIGHT JS SAVINELL RF LITT M
Citation: Jj. Fontanella et al., HIGH-PRESSURE ELECTRICAL-CONDUCTIVITY STUDIES OF ACID DOPED POLYBENZIMIDAZOLE, Electrochimica acta, 43(10-11), 1998, pp. 1289-1294
HOMOZYGOSITY MAPPING OF THE GENE FOR HALLERVODEN-SPATZ-SYNDROME TO CHROMOSOME-20P12.3-P13 (VOL 14, PG 479, 1996)
Authors: TAYLOR T LITT M KRAMER P PANDOLFO M ANGELINI L NARDOCCI N PINEDA M DAVIES S HATTORI H FLETT PJ CILIO MR BERTINI E HAYFLICK SJ
Citation: T. Taylor et al., HOMOZYGOSITY MAPPING OF THE GENE FOR HALLERVODEN-SPATZ-SYNDROME TO CHROMOSOME-20P12.3-P13 (VOL 14, PG 479, 1996), Nature genetics, 16(1), 1997, pp. 109-109
PROJECT MATCH SECONDARY A-PRIORI HYPOTHESES
Authors: ALLEN J ANTON RF BABOR TF CARBONARI J CARROLL KM CONNORS GJ COONEY NL DELBOCA FK DICLEMENTE CC DONOVAN D KADDEN RM LITT M LONGABAUGH R MATTSON M MILLER WR RANDALL CL ROUNSAVILLE BJ RYCHTARIK RG STOUT RL TONIGAN JS WIRTZ PW ZWEBEN A
Citation: J. Allen et al., PROJECT MATCH SECONDARY A-PRIORI HYPOTHESES, Addiction, 92(12), 1997, pp. 1671-1698
AUTOSOMAL-DOMINANT CERULEAN CATARACT IS ASSOCIATED WITH A CHAIN TERMINATION MUTATION IN THE HUMAN BETA-CRYSTALLIN GENE CRYBB2
Authors: LITT M CARREROVALENZUELA R LAMORTICELLA DM SCHULTZ DW MITCHELL TN KRAMER P MAUMENEE IH
Citation: M. Litt et al., AUTOSOMAL-DOMINANT CERULEAN CATARACT IS ASSOCIATED WITH A CHAIN TERMINATION MUTATION IN THE HUMAN BETA-CRYSTALLIN GENE CRYBB2, Human molecular genetics, 6(5), 1997, pp. 665-668
MODULATION OF THE AGE AT ONSET OF PARKINSONS-DISEASE BY APOLIPOPROTEIN-E GENOTYPES
Authors: ZAREPARSI S KAYE J CAMICIOLI R GRIMSLID H OKEN B LITT M NUTT J BIRD T SCHELLENBERG G PAYAMI H
Citation: S. Zareparsi et al., MODULATION OF THE AGE AT ONSET OF PARKINSONS-DISEASE BY APOLIPOPROTEIN-E GENOTYPES, Annals of neurology, 42(4), 1997, pp. 655-658
A FOUNDER MUTATION IN TIMP3, SER181CYS, PRESENTS WITH VARIABLE EXPRESSIVITY OF SORSBYS FUNDUS DYSTROPHY
Authors: FELBOR U BENKWITZ C LITT M GREENBERG J GREGORY CY WEBER BHF
Citation: U. Felbor et al., A FOUNDER MUTATION IN TIMP3, SER181CYS, PRESENTS WITH VARIABLE EXPRESSIVITY OF SORSBYS FUNDUS DYSTROPHY, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3711-3711
MATCHING ALCOHOLISM TREATMENTS TO CLIENT HETEROGENEITY - PROJECT MATCH POSTTREATMENT DRINKING OUTCOMES
Authors: ALLEN JP MATTSON ME MILLER WR TONIGAN JS CONNORS GJ RYCHTARIK RG RANDALL CL ANTON RF KADDEN RM LITT M COONEY NL DICLEMENTE CC CARBONARI J ZWEBEN A LONGABAUGH RH STOUT RL DONOVAN D BABOR TF DELBOCA FK ROUNSAVILLE BJ CARROLL KM WIRTZ PW BAILEY S BRADY K CISLER R HESTER RK KIVLAHAN DR NIRENBERG TD PATE LA STURGIS E MUENZ L CUSHMAN P FINNEY J HINGSON R KLETT J TOWNSEND M
Citation: Jp. Allen et al., MATCHING ALCOHOLISM TREATMENTS TO CLIENT HETEROGENEITY - PROJECT MATCH POSTTREATMENT DRINKING OUTCOMES, Journal of studies on alcohol, 58(1), 1997, pp. 7-29
INVASIVE INFECTIONS DUE TO A FISH PATHOGEN, STREPTOCOCCUS-INIAE
Authors: WEINSTEIN MR LITT M KERTESZ DA WYPER P ROSE D COULTER M MCGEER A FACKLAM R OSTACH C WILLEY BM BORCZYK A LOW DE
Citation: Mr. Weinstein et al., INVASIVE INFECTIONS DUE TO A FISH PATHOGEN, STREPTOCOCCUS-INIAE, The New England journal of medicine, 337(9), 1997, pp. 589-594
CAUSAL EXPLANATIONS FOR ILLNESS, COPING, AND DISTRESS IN TMD PATIENTS
Authors: LITT M KALINOWSKI L
Citation: M. Litt et L. Kalinowski, CAUSAL EXPLANATIONS FOR ILLNESS, COPING, AND DISTRESS IN TMD PATIENTS, Journal of dental research, 76, 1997, pp. 2541-2541
ORAL HEALTH BELIEFS, BEHAVIOR, AND, MUTANS STREP, PREVALENCE IN CHILDREN ENROLLED IN WIC
Authors: REISINE S LITT M DOUGLASS J OSULLIVAN D DALEY N NELSON E BROWNE A STRICKLAND M TINANOFF N
Citation: S. Reisine et al., ORAL HEALTH BELIEFS, BEHAVIOR, AND, MUTANS STREP, PREVALENCE IN CHILDREN ENROLLED IN WIC, Journal of dental research, 76, 1997, pp. 2545-2545
POSTTRAUMATIC-STRESS-DISORDER IN CHILD WITNESSES TO DOMESTIC VIOLENCE
Authors: KILPATRICK KL LITT M WILLIAMS LM
Citation: Kl. Kilpatrick et al., POSTTRAUMATIC-STRESS-DISORDER IN CHILD WITNESSES TO DOMESTIC VIOLENCE, American journal of orthopsychiatry, 67(4), 1997, pp. 639-644
EXCLUSION OF THE LOCUS FOR PARKINSONS-DISEASE ON CHROMOSOME-4 IN 3 FAMILIES
Authors: KRAMER P ZAREPARSI S KAYE J CAMICIOLI R NUTT J LITT M PAYAMI H
Citation: P. Kramer et al., EXCLUSION OF THE LOCUS FOR PARKINSONS-DISEASE ON CHROMOSOME-4 IN 3 FAMILIES, American journal of human genetics, 61(4), 1997, pp. 1639-1639
EVIDENCE FOR LOCUS HETEROGENEITY IN HALLERVORDEN-SPATZ-SYNDROME
Authors: TAYLOR TD HATTORI H BUNDEY S MALANDRINI A VILLANOVA M FABRIZI GM MALONE A LITT M HAYFLICK SJ
Citation: Td. Taylor et al., EVIDENCE FOR LOCUS HETEROGENEITY IN HALLERVORDEN-SPATZ-SYNDROME, American journal of human genetics, 61(4), 1997, pp. 2357-2357
HOMOZYGOSITY MAPPING OF HALLERVORDEN-SPATZ SYNDROME TO CHROMOSOME 20P12.3-P13
Authors: TAYLOR TD LITT M KRAMER P PANDOLFO M ANGELINI L NARDOCCI N DAVIS S PINEDA M HATTORI H FLETT PJ CILIO MR BERTINI E HAYFLICK SJ
Citation: Td. Taylor et al., HOMOZYGOSITY MAPPING OF HALLERVORDEN-SPATZ SYNDROME TO CHROMOSOME 20P12.3-P13, Nature genetics, 14(4), 1996, pp. 479-481
A 3-MB REGION FOR THE FAMILIAL HEMIPLEGIC MIGRAINE LOCUS ON 19P13.1-P13.2 - EXCLUSION OF PRKCSH AS A CANDIDATE GENE
Authors: OPHOFF RA TERWINDT GM VERGOUWE MN VANEIJK R MOHRENWEISER H LITT M HOFKER MH HAAN J FERRARI MD FRANTS RR
Citation: Ra. Ophoff et al., A 3-MB REGION FOR THE FAMILIAL HEMIPLEGIC MIGRAINE LOCUS ON 19P13.1-P13.2 - EXCLUSION OF PRKCSH AS A CANDIDATE GENE, European journal of human genetics, 4(6), 1996, pp. 321-328
A HIGH-RESOLUTION CEPH CROSSOVER MAPPING PANEL AND INTEGRATED MAP OF CHROMOSOME-11
Authors: FAIN PR KORT EN YOUSRY C JAMES MR LITT M
Citation: Pr. Fain et al., A HIGH-RESOLUTION CEPH CROSSOVER MAPPING PANEL AND INTEGRATED MAP OF CHROMOSOME-11, Human molecular genetics, 5(10), 1996, pp. 1631-1636
A 2ND GENE FOR CERULEAN CATARACTS MAPS TO THE BETA-CRYSTALLIN REGION ON CHROMOSOME-22
Authors: KRAMER P YOUNT J MITCHELL T LAMORTICELLA D CARREROVALENZUELA R LOVRIEN E MAUMENEE I LITT M
Citation: P. Kramer et al., A 2ND GENE FOR CERULEAN CATARACTS MAPS TO THE BETA-CRYSTALLIN REGION ON CHROMOSOME-22, Genomics, 35(3), 1996, pp. 539-542
LOCALIZATION OF 2 POTASSIUM CHANNEL BETA-SUBUNIT GENES, KCNA1B AND KCNA2B
Authors: SCHULTZ D LITT M SMITH L THAYER M MCCORMACK K
Citation: D. Schultz et al., LOCALIZATION OF 2 POTASSIUM CHANNEL BETA-SUBUNIT GENES, KCNA1B AND KCNA2B, Genomics, 31(3), 1996, pp. 389-391
REPORT OF THE 5TH INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-11 MAPPING (1996)
Authors: SHOWS TB ALDERS M BENNETT S BURBEE D CARTWRIGHT P CHANDRASEKHARAPPA S COOPER P COURSEAUX A DAVIES C DEVIGNES MD DEVILEE P ELLIOTT R EVANS G FANTES J GARNER H GAUDRAY P GERHARD DS GESSLER M HIGGINS M HUMMERICH H JAMES M LAGERCRANTZ J LITT M LITTLE P MANNENS M MUNROE D NOWAK N OBRIEN S PARKER N PERLIN M REID L RICHARD C SAWICKI M SWALLOW D THAKKER R VANHEYNINGEN V VANSCHOTHORST E VORECHOVSKY I WADELIUS C WEBER B ZABEL B
Citation: Tb. Shows et al., REPORT OF THE 5TH INTERNATIONAL WORKSHOP ON HUMAN-CHROMOSOME-11 MAPPING (1996), Cytogenetics and cell genetics, 74(1-2), 1996, pp. 2-52
FAMILIAL PARKINSONS-DISEASE, DEMENTIA, AND APOLIPOPROTEIN-E
Authors: ZAREPARSI S GRIMSLID H NUTT J LITT M KAYE J PAYAMI H
Citation: S. Zareparsi et al., FAMILIAL PARKINSONS-DISEASE, DEMENTIA, AND APOLIPOPROTEIN-E, Neurology, 46(2), 1996, pp. 2067-2067
Risultati: 1-25 | 26-50 | 51-75