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Results: 1-25 | 26-50 | 51-59
Results: 1-25/59
SUN-RELATED RISK-FACTORS IN MELANOMA-PRONE FAMILIES WITH CDKN2A MUTATIONS
Authors: GOLDSTEIN AM FALK RT FRASER MC DRACOPOLI NC SIKORSKI RS CLARK WH TUCKER MA
Citation: Am. Goldstein et al., SUN-RELATED RISK-FACTORS IN MELANOMA-PRONE FAMILIES WITH CDKN2A MUTATIONS, Journal of the National Cancer Institute, 90(9), 1998, pp. 709-711
HAPLOTYPE ANALYSIS OF 2 RECURRENT CDKN2A MUTATIONS IN 10 MELANOMA FAMILIES - EVIDENCE FOR COMMON FOUNDERS AND INDEPENDENT MUTATIONS
Authors: POLLOCK PM SPURR N BISHOP T NEWTONBISHOP J GRUIS N VANDERVELDEN PA GOLDSTEIN AM TUCKER MA FOULKES WD BARNHILL R HABER D FOUNTAIN J HAYWARD NK
Citation: Pm. Pollock et al., HAPLOTYPE ANALYSIS OF 2 RECURRENT CDKN2A MUTATIONS IN 10 MELANOMA FAMILIES - EVIDENCE FOR COMMON FOUNDERS AND INDEPENDENT MUTATIONS, Human mutation, 11(6), 1998, pp. 424-431
ALLELIC IMBALANCE, INCLUDING DELETION OF PTEN MMACI, AT THE COWDEN DISEASE LOCUS ON 10Q22-23, IN HAMARTOMAS FROM PATIENTS WITH COWDEN SYNDROME AND GERMLINE PTEN MUTATION/
Authors: MARSH DJ DAHIA PLM COULON V ZHENG ZM DORIONBONNET F CALL KM LITTLE R LIN AY EELES RA GOLDSTEIN AM HODGSON SV RICHARDSON AL ROBINSON BG WEBER HC LONGY M ENG C
Citation: Dj. Marsh et al., ALLELIC IMBALANCE, INCLUDING DELETION OF PTEN MMACI, AT THE COWDEN DISEASE LOCUS ON 10Q22-23, IN HAMARTOMAS FROM PATIENTS WITH COWDEN SYNDROME AND GERMLINE PTEN MUTATION/, Genes, chromosomes & cancer, 21(1), 1998, pp. 61-69
RPA2, A GENE FOR THE 32 KDA SUBUNIT OF REPLICATION PROTEIN-A ON CHROMOSOME 1P35-36, IS NOT MUTATED IN PATIENTS WITH FAMILIAL MELANOMA LINKED TO CHROMOSOME 1P36
Authors: PING YJ NAKATSU Y GOLDSTEIN AM TUCKER MA KRAEMER KH TANAKA K
Citation: Yj. Ping et al., RPA2, A GENE FOR THE 32 KDA SUBUNIT OF REPLICATION PROTEIN-A ON CHROMOSOME 1P35-36, IS NOT MUTATED IN PATIENTS WITH FAMILIAL MELANOMA LINKED TO CHROMOSOME 1P36, Melanoma research, 8(1), 1998, pp. 47-52
PATTERNING THE HEARTS LEFT-RIGHT AXIS - FROM ZEBRAFISH TO MAN
Authors: GOLDSTEIN AM TICHO BS FISHMAN MC
Citation: Am. Goldstein et al., PATTERNING THE HEARTS LEFT-RIGHT AXIS - FROM ZEBRAFISH TO MAN, Developmental genetics, 22(3), 1998, pp. 278-287
FAMILIAL EOSINOPHILIA - CLINICAL AND LABORATORY RESULTS ON A US KINDRED
Authors: LIN AY NUTMAN TB KASLOW D MULVIHILL JJ FONTAINE L WHITE BJ KNUTSEN T THEIL KS RAGHUPRASAD PK GOLDSTEIN AM TUCKER MA
Citation: Ay. Lin et al., FAMILIAL EOSINOPHILIA - CLINICAL AND LABORATORY RESULTS ON A US KINDRED, American journal of medical genetics, 76(3), 1998, pp. 229-237
DISORDERS OF LEFT-RIGHT DEVELOPMENT - CAUSES AND CONSEQUENCES
Authors: GOLDSTEIN AM CHEN JN VANPRAAGH R TICHO BS FISHMAN MC
Citation: Am. Goldstein et al., DISORDERS OF LEFT-RIGHT DEVELOPMENT - CAUSES AND CONSEQUENCES, Pediatrics (Evanston), 102(3), 1998, pp. 804-804
CDKN2A MUTATIONS IN MULTIPLE PRIMARY MELANOMAS
Authors: MONZON J LIU L BRILL H GOLDSTEIN AM TUCKER MA FROM L MCLAUGHLIN J HOGG D LASSAM NJ
Citation: J. Monzon et al., CDKN2A MUTATIONS IN MULTIPLE PRIMARY MELANOMAS, The New England journal of medicine, 338(13), 1998, pp. 879-887
JUNCTIONAL EPIDERMOLYSIS-BULLOSA - DIAGNOSIS AND MANAGEMENT OF A PATIENT WITH THE HERLITZ VARIANT
Authors: GOLDSTEIN AM DAVENPORT T SHERIDAN RL
Citation: Am. Goldstein et al., JUNCTIONAL EPIDERMOLYSIS-BULLOSA - DIAGNOSIS AND MANAGEMENT OF A PATIENT WITH THE HERLITZ VARIANT, Journal of pediatric surgery, 33(5), 1998, pp. 756-758
NOTOCHORD REGULATES CARDIAC LINEAGE IN ZEBRAFISH EMBRYOS
Authors: GOLDSTEIN AM FISHMAN MC
Citation: Am. Goldstein et Mc. Fishman, NOTOCHORD REGULATES CARDIAC LINEAGE IN ZEBRAFISH EMBRYOS, Developmental biology (Print), 201(2), 1998, pp. 247-252
FAMILIAL EOSINOPHILIA MAPS TO THE CYTOKINE GENE-CLUSTER ON HUMAN CHROMOSOMAL REGION 5Q31-Q33
Authors: RIOUX JD STONE VA DALY MJ CARGILL M GREEN T NGUYEN H NUTMAN T ZIMMERMAN PA TUCKER MA HUDSON T GOLDSTEIN AM LANDER E LIN AY
Citation: Jd. Rioux et al., FAMILIAL EOSINOPHILIA MAPS TO THE CYTOKINE GENE-CLUSTER ON HUMAN CHROMOSOMAL REGION 5Q31-Q33, American journal of human genetics, 63(4), 1998, pp. 1086-1094
SCREENING FOR CDKN2A MUTATIONS IN HEREDITARY MELANOMA
Authors: GOLDSTEIN AM TUCKER MA
Citation: Am. Goldstein et Ma. Tucker, SCREENING FOR CDKN2A MUTATIONS IN HEREDITARY MELANOMA, Journal of the National Cancer Institute, 89(10), 1997, pp. 676-678
AFFECTED MEMBERS OF MELANOMA-PRONE FAMILIES WITH LINKAGE TO 9P21 BUT LACKING MUTATIONS IN CDKN2A DO NOT HARBOR MUTATIONS IN THE CODING REGIONS OF EITHER CDKN2B OR P19(ARF)
Authors: LIU L GOLDSTEIN AM TUCKER MA BRILL H GRUIS NA HOGG D LASSAM NJ
Citation: L. Liu et al., AFFECTED MEMBERS OF MELANOMA-PRONE FAMILIES WITH LINKAGE TO 9P21 BUT LACKING MUTATIONS IN CDKN2A DO NOT HARBOR MUTATIONS IN THE CODING REGIONS OF EITHER CDKN2B OR P19(ARF), Genes, chromosomes & cancer, 19(1), 1997, pp. 52-54
2ND CANCERS AFTER MEDULLOBLASTOMA - POPULATION-BASED RESULTS FROM THEUNITED-STATES AND SWEDEN
Authors: GOLDSTEIN AM YUEN J TUCKER MA
Citation: Am. Goldstein et al., 2ND CANCERS AFTER MEDULLOBLASTOMA - POPULATION-BASED RESULTS FROM THEUNITED-STATES AND SWEDEN, CCC. Cancer causes & control, 8(6), 1997, pp. 865-871
DETECTION OF GENES FOR COMPLEX TRAITS - PREFACE
Authors: GOLDIN LR BAILEYWILSON JE BORECKI IB FALK CT GOLDSTEIN AM SUAREZ BK MACCLUER JW
Citation: Lr. Goldin et al., DETECTION OF GENES FOR COMPLEX TRAITS - PREFACE, Genetic epidemiology, 14(6), 1997, pp. 25-26
SIB-PAIR LINKAGE ANALYSES OF NUCLEAR FAMILY DATA - QUANTITATIVE VERSUS DICHOTOMOUS DISEASE CLASSIFICATION
Authors: KORCZAK JF GOLDSTEIN AM
Citation: Jf. Korczak et Am. Goldstein, SIB-PAIR LINKAGE ANALYSES OF NUCLEAR FAMILY DATA - QUANTITATIVE VERSUS DICHOTOMOUS DISEASE CLASSIFICATION, Genetic epidemiology, 14(6), 1997, pp. 827-832
DETECTING GENE-ENVIRONMENT INTERACTIONS USING A CASE-CONTROL DESIGN
Authors: GOLDSTEIN AM FALK RT KORCZAK JF LUBIN JH
Citation: Am. Goldstein et al., DETECTING GENE-ENVIRONMENT INTERACTIONS USING A CASE-CONTROL DESIGN, Genetic epidemiology, 14(6), 1997, pp. 1085-1089
CLINICAL MANIFESTATIONS IN 105 PERSONS WITH NEVOID BASAL-CELL CARCINOMA SYNDROME
Authors: KIMONIS VE GOLDSTEIN AM PASTAKIA B YANG ML KASE R DIGIOVANNA JJ BALE AE BALE SJ
Citation: Ve. Kimonis et al., CLINICAL MANIFESTATIONS IN 105 PERSONS WITH NEVOID BASAL-CELL CARCINOMA SYNDROME, American journal of medical genetics, 69(3), 1997, pp. 299-308
NEVOID BASAL-CELL CARCINOMA SYNDROME WITH MEDULLOBLASTOMA IN AN AFRICAN-AMERICAN BOY - A RARE CASE ILLUSTRATING GENE-ENVIRONMENT INTERACTION
Authors: KORCZAK JF BRAHIM JS DIGIOVANNA JJ KASE RG WEXLER LH GOLDSTEIN AM
Citation: Jf. Korczak et al., NEVOID BASAL-CELL CARCINOMA SYNDROME WITH MEDULLOBLASTOMA IN AN AFRICAN-AMERICAN BOY - A RARE CASE ILLUSTRATING GENE-ENVIRONMENT INTERACTION, American journal of medical genetics, 69(3), 1997, pp. 309-314
FEMORAL VENOUS ACCESS IS SAFE IN BURNED CHILDREN - AN ANALYSIS OF 224CATHETERS
Authors: GOLDSTEIN AM WEBER JM SHERIDAN RL
Citation: Am. Goldstein et al., FEMORAL VENOUS ACCESS IS SAFE IN BURNED CHILDREN - AN ANALYSIS OF 224CATHETERS, The Journal of pediatrics, 130(3), 1997, pp. 442-446
HYPERMUTABILITY OF UV-TREATED PLASMIDS IN DYSPLASTIC NEVUS FAMILIAL MELANOMA CELL-LINES/
Authors: MORIWAKI SI TARONE RE TUCKER MA GOLDSTEIN AM KRAEMER KH
Citation: Si. Moriwaki et al., HYPERMUTABILITY OF UV-TREATED PLASMIDS IN DYSPLASTIC NEVUS FAMILIAL MELANOMA CELL-LINES/, Cancer research, 57(20), 1997, pp. 4637-4641
A GENE FOR FAMILIAR EOSINOPHILIA MAPS TO CHROMOSOME 5Q31-Q33
Authors: LIN AY RIOUX JD NUTMAN T DALY M STONE V NGUYEN H GREEN T HUDSON T ZIMMERMAN PA FONTAINE L TUCKER MA LANDER E GOLDSTEIN AM
Citation: Ay. Lin et al., A GENE FOR FAMILIAR EOSINOPHILIA MAPS TO CHROMOSOME 5Q31-Q33, American journal of human genetics, 61(4), 1997, pp. 1648-1648
GENOMIC SCREEN FOR LINKAGE IN A FAMILY WITH AUTOSOMAL-DOMINANT CHORDOMA
Authors: KORCZAK JF KELLEY MJ ALLIKIAN KA SHAH AA GOLDSTEIN AM PARRY DM
Citation: Jf. Korczak et al., GENOMIC SCREEN FOR LINKAGE IN A FAMILY WITH AUTOSOMAL-DOMINANT CHORDOMA, American journal of human genetics, 61(4), 1997, pp. 2343-2343
VALIDATION OF FAMILY HISTORY OF CANCER IN DECEASED FAMILY MEMBERS
Authors: NOVAKOVIC B GOLDSTEIN AM TUCKER MG
Citation: B. Novakovic et al., VALIDATION OF FAMILY HISTORY OF CANCER IN DECEASED FAMILY MEMBERS, Journal of the National Cancer Institute, 88(20), 1996, pp. 1492-1493
LOCALIZATION OF THE GENE FOR COWDEN DISEASE TO CHROMOSOME 10Q22-23
Authors: NELEN MR PADBERG GW PEETERS EAJ LIN AY VANDENHELM B FRANTS RR COULON V GOLDSTEIN AM VANREEN MMM EASTON DF EELES RA HODGSON S MULVIHILL JJ MURDAY VA TUCKER MA MARIMAN ECM STARINK TM PONDER BAJ ROPERS HH KREMER H LONGY M ENG C
Citation: Mr. Nelen et al., LOCALIZATION OF THE GENE FOR COWDEN DISEASE TO CHROMOSOME 10Q22-23, Nature genetics, 13(1), 1996, pp. 114-116
Risultati: 1-25 | 26-50 | 51-59