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Results: 26-50/155
HUMAN UTEROGLOBIN GENE - STRUCTURE, SUBCHROMOSOMAL LOCALIZATION, AND POLYMORPHISM
Authors: ZHANG ZJ ZIMONJIC DB POPESCU NC WANG N GERHARD DS STONE EM ARBOUR NC DEVRIES HG SCHEFFER H GERRITSEN J COLLEE JM TENKATE LP MUKHERJEE AB
Citation: Zj. Zhang et al., HUMAN UTEROGLOBIN GENE - STRUCTURE, SUBCHROMOSOMAL LOCALIZATION, AND POLYMORPHISM, DNA and cell biology, 16(1), 1997, pp. 73-83
FAMILIAL HYPOMAGNESEMIA MAPS TO CHROMOSOME 9Q, NOT TO THE X-CHROMOSOME - GENETIC-LINKAGE MAPPING AND ANALYSIS OF A BALANCED TRANSLOCATION BREAKPOINT
Authors: WALDER RY SHALEV H BRENNAN TMH CARMI R ELBEDOUR K SCOTT DA HANAUER A MARK AL PATIL S STONE EM SHEFFIELD VC
Citation: Ry. Walder et al., FAMILIAL HYPOMAGNESEMIA MAPS TO CHROMOSOME 9Q, NOT TO THE X-CHROMOSOME - GENETIC-LINKAGE MAPPING AND ANALYSIS OF A BALANCED TRANSLOCATION BREAKPOINT, Human molecular genetics, 6(9), 1997, pp. 1491-1497
HOMOZYGOSITY MAPPING OF ACHROMATOPSIA TO CHROMOSOME-2 USING DNA POOLING
Authors: ARBOUR NC ZLOTOGORA J KNOWLTON RG MERIN S ROSENMANN A KANIS AB ROKHLINA T STONE EM SHEFFIELD VC
Citation: Nc. Arbour et al., HOMOZYGOSITY MAPPING OF ACHROMATOPSIA TO CHROMOSOME-2 USING DNA POOLING, Human molecular genetics, 6(5), 1997, pp. 689-694
IRAQI-JEWISH KINDREDS WITH OPTIC ATROPHY PLUS (3-METHYLGLUTACONIC ACIDURIA TYPE-3) DEMONSTRATE LINKAGE DISEQUILIBRIUM WITH THE CTG REPEAT IN THE 3'-UNTRANSLATED REGION OF THE MYOTONIC-DYSTROPHY PROTEIN-KINASE GENE
Authors: NYSTUEN A COSTEFF H ELPELEG ON APTER N BONNETAMIR B MOHRENWEISER H HAIDER N STONE EM SHEFFIELD VC
Citation: A. Nystuen et al., IRAQI-JEWISH KINDREDS WITH OPTIC ATROPHY PLUS (3-METHYLGLUTACONIC ACIDURIA TYPE-3) DEMONSTRATE LINKAGE DISEQUILIBRIUM WITH THE CTG REPEAT IN THE 3'-UNTRANSLATED REGION OF THE MYOTONIC-DYSTROPHY PROTEIN-KINASE GENE, Human molecular genetics, 6(4), 1997, pp. 563-569
IDENTIFICATION OF A COMPLEX CONGENITAL HEART DEFECT SUSCEPTIBILITY LOCUS BY USING DNA POOLING AND SHARED SEGMENT ANALYSIS
Authors: SHEFFIELD VC PIERPONT ME NISHIMURA D BEEK JS BURNS TL BERG MA STONE EM PATIL SR LAUER RM
Citation: Vc. Sheffield et al., IDENTIFICATION OF A COMPLEX CONGENITAL HEART DEFECT SUSCEPTIBILITY LOCUS BY USING DNA POOLING AND SHARED SEGMENT ANALYSIS, Human molecular genetics, 6(1), 1997, pp. 117-121
CHOOSING A HEALTH PLAN - WHAT INFORMATION WILL CONSUMERS USE
Authors: TUMLINSON A BOTTIGHEIMER H MAHONEY P STONE EM HENDRICKS A
Citation: A. Tumlinson et al., CHOOSING A HEALTH PLAN - WHAT INFORMATION WILL CONSUMERS USE, Health affairs, 16(3), 1997, pp. 229-238
SERINE-27-PHENYLALANINE MUTATION WITHIN THE PERIPHERIN RDS GENE IN A FAMILY WITH CONE DYSTROPHY/
Authors: FISHMAN GA STONE EM ALEXANDER KR GILBERT LD DERLACKI DJ BUTLER NS
Citation: Ga. Fishman et al., SERINE-27-PHENYLALANINE MUTATION WITHIN THE PERIPHERIN RDS GENE IN A FAMILY WITH CONE DYSTROPHY/, Ophthalmology, 104(2), 1997, pp. 299-306
HOMOZYGOSITY MAPPING OF ACHROMATOPSIA TO CHROMOSOME 2P11 USING DNA POOLING
Authors: ARBOUR NC ZLOTOGORA J KNOWLTON RG MERIN S ROKHLINA T STONE EM SHEFFIELD VC
Citation: Nc. Arbour et al., HOMOZYGOSITY MAPPING OF ACHROMATOPSIA TO CHROMOSOME 2P11 USING DNA POOLING, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3295-3295
CLINICAL CHARACTERIZATION OF A 2ND FAMILY WITH AUTOSOMAL-DOMINANT NEOVASCULAR INFLAMMATORY VITREORETINOPATHY (ADNIV) AND FINE MAPPING OF THE DISEASE INTERVAL
Authors: SONKIN PL BROWN J FOLK JC TAYLOR CM AFFATIGATO LM SHEFFIELD VC STONE EM
Citation: Pl. Sonkin et al., CLINICAL CHARACTERIZATION OF A 2ND FAMILY WITH AUTOSOMAL-DOMINANT NEOVASCULAR INFLAMMATORY VITREORETINOPATHY (ADNIV) AND FINE MAPPING OF THE DISEASE INTERVAL, Investigative ophthalmology & visual science, 38(4), 1997, pp. 3697-3697
IDENTIFICATION OF THE GENE CAUSING 1Q-LINKED JUVENILE-ONSET OPEN-ANGLE GLAUCOMA (GLC1A) AND EVIDENCE FOR ITS INVOLVEMENT IN ADULT PRIMARY OPEN-ANGLE GLAUCOMA
Authors: FINGERT JH ALWARD WLM SUNDEN SLF NISHIMURA D NYSTUEN A NICHOLS BE MACKEY DA RITCH R KALENAK JW CRAVEN ER BECK GE STREB LM SHEFFIELD VC STONE EM
Citation: Jh. Fingert et al., IDENTIFICATION OF THE GENE CAUSING 1Q-LINKED JUVENILE-ONSET OPEN-ANGLE GLAUCOMA (GLC1A) AND EVIDENCE FOR ITS INVOLVEMENT IN ADULT PRIMARY OPEN-ANGLE GLAUCOMA, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4333-4333
THE PHENOTYPE OF PRIMARY OPEN-ANGLE GLAUCOMA PATIENT WITH MUTATIONS IN THE GLC1A GENE
Authors: ALWARD WLM FINGERT JH JOHNSON AT KWON YH HAYREH SS LOVE TM VANDENBURGH K SHEFFIELD VC STONE EM
Citation: Wlm. Alward et al., THE PHENOTYPE OF PRIMARY OPEN-ANGLE GLAUCOMA PATIENT WITH MUTATIONS IN THE GLC1A GENE, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4335-4335
TONOGRAPHY IN A PRIMARY OPEN-ANGLE GLAUCOMA (POAG) PEDIGREE LINKING TO GLC1A
Authors: WILKINSON CH WONG TL DEVEREUX C STOREY I MCCARTNEY PJ COOPER RL MACKEY DA STONE EM SHEFFIELD VC COOTE MA
Citation: Ch. Wilkinson et al., TONOGRAPHY IN A PRIMARY OPEN-ANGLE GLAUCOMA (POAG) PEDIGREE LINKING TO GLC1A, Investigative ophthalmology & visual science, 38(4), 1997, pp. 4922-4922
CLINICAL CHARACTERIZATION AND LINKAGE ANALYSIS OF A 4 GENERATION FAMILY WITH CONE-ROD DYSTROPHY
Authors: BROWN J NICHOLS BE WILES CD BUTLER N SHEFFIELD VC STONE EM
Citation: J. Brown et al., CLINICAL CHARACTERIZATION AND LINKAGE ANALYSIS OF A 4 GENERATION FAMILY WITH CONE-ROD DYSTROPHY, Investigative ophthalmology & visual science, 38(4), 1997, pp. 5339-5339
A SYNDROME INVOLVING OPTIC ATROPHY DEMONSTRATES LINKAGE DISEQUILIBRIUM WITH THE CTG REPEAT IN THE 3' UNTRANSLATED REGION OF THE MYOTONIC-DYSTROPHY PROTEIN-KINASE GENE
Authors: NYSTUEN A COSTEFF H BONNETAMIR B HAIDER N MOHRENWEISER H STONE EM SHEFFIELD VC
Citation: A. Nystuen et al., A SYNDROME INVOLVING OPTIC ATROPHY DEMONSTRATES LINKAGE DISEQUILIBRIUM WITH THE CTG REPEAT IN THE 3' UNTRANSLATED REGION OF THE MYOTONIC-DYSTROPHY PROTEIN-KINASE GENE, Investigative ophthalmology & visual science, 38(4), 1997, pp. 1822-1822
MOLECULAR ANALYSES OF IPM-150, A PHOTORECEPTOR CELL-SPECIFIC PROTEOGLYCAN
Authors: KUEHN MH STONE EM HAGEMAN GS
Citation: Mh. Kuehn et al., MOLECULAR ANALYSES OF IPM-150, A PHOTORECEPTOR CELL-SPECIFIC PROTEOGLYCAN, Investigative ophthalmology & visual science, 38(4), 1997, pp. 2788-2788
DNA-DAMAGE IN BREAST EPITHELIAL-CELLS - DETECTION BY THE SINGLE-CELL GEL (COMET) ASSAY AND INDUCTION BY HUMAN MAMMARY LIPID EXTRACTS
Authors: MARTIN FL VENITT S CARMICHAEL PL CROFTONSLEIGH C STONE EM COLE KJ GUSTERSON BA GROVER PL PHILLIPS DH
Citation: Fl. Martin et al., DNA-DAMAGE IN BREAST EPITHELIAL-CELLS - DETECTION BY THE SINGLE-CELL GEL (COMET) ASSAY AND INDUCTION BY HUMAN MAMMARY LIPID EXTRACTS, Carcinogenesis, 18(12), 1997, pp. 2299-2305
IDENTIFICATION OF A GENE THAT CAUSES PRIMARY OPEN-ANGLE GLAUCOMA
Authors: STONE EM FINGERT JH ALWARD WLM NGUYEN TD POLANSKY JR SUNDEN SLF NISHIMURA D CLARK AF NYSTUEN A NICHOLS BE MACKEY DA RITCH R KALENAK JW CRAVEN ER SHEFFIELD VC
Citation: Em. Stone et al., IDENTIFICATION OF A GENE THAT CAUSES PRIMARY OPEN-ANGLE GLAUCOMA, Science, 275(5300), 1997, pp. 668-670
CLINICAL AND GENETIC-ANALYSIS OF A FAMILY AFFECTED WITH DOMINANT ATROPHY (OPA1) (VOL 115, PG 95, 1997)
Authors: BROWN J FINGERT JH TAYLOR CM LAKE M SHEFFIELD VC STONE EM
Citation: J. Brown et al., CLINICAL AND GENETIC-ANALYSIS OF A FAMILY AFFECTED WITH DOMINANT ATROPHY (OPA1) (VOL 115, PG 95, 1997), Archives of ophthalmology, 115(5), 1997, pp. 663-663
X-LINKED RETINITIS-PIGMENTOSA ASSOCIATED WITH A 2-BASE PAIR INSERTIONIN CODON-99 OF THE RP3 GENE RPGR
Authors: WELEBER RG BUTLER NS MURPHEY WH SHEFFIELD VC STONE EM
Citation: Rg. Weleber et al., X-LINKED RETINITIS-PIGMENTOSA ASSOCIATED WITH A 2-BASE PAIR INSERTIONIN CODON-99 OF THE RP3 GENE RPGR, Archives of ophthalmology, 115(11), 1997, pp. 1429-1435
FLUCTUATING VISION IN BEST-DISEASE
Authors: PARK DW POLK TD STONE EM
Citation: Dw. Park et al., FLUCTUATING VISION IN BEST-DISEASE, Archives of ophthalmology, 115(11), 1997, pp. 1469-1470
MULTIPLE EVANESCENT WHITE DOT SYNDROME IN A PATIENT WITH BEST-DISEASE
Authors: PARK DW POLK TD STONE EM
Citation: Dw. Park et al., MULTIPLE EVANESCENT WHITE DOT SYNDROME IN A PATIENT WITH BEST-DISEASE, Archives of ophthalmology, 115(10), 1997, pp. 1342-1343
CLINICAL AND GENETIC-ANALYSIS OF A FAMILY AFFECTED WITH DOMINANT OPTIC ATROPHY (OPA1)
Authors: BROWN J FINGERT JH TAYLOR CM LAKE M SHEFFIELD VC STONE EM
Citation: J. Brown et al., CLINICAL AND GENETIC-ANALYSIS OF A FAMILY AFFECTED WITH DOMINANT OPTIC ATROPHY (OPA1), Archives of ophthalmology, 115(1), 1997, pp. 95-99
CHARACTERIZATION OF THE GLAUCOMA PHENOTYPES ASSOCIATED WITH 2 MUTATIONS IN THE GLC1A GENE
Authors: FINGERT JH CLARK TD BECK G HOCKEY R ALWARD WLM SHEFFIELD VC STONE EM
Citation: Jh. Fingert et al., CHARACTERIZATION OF THE GLAUCOMA PHENOTYPES ASSOCIATED WITH 2 MUTATIONS IN THE GLC1A GENE, American journal of human genetics, 61(4), 1997, pp. 102-102
CHARACTERIZATION OF 6P25 CHROMOSOMAL-ANOMALIES IN 2 PATIENTS IDENTIFIES A POTENTIAL CANDIDATE GENE CAUSING CONGENITAL GLAUCOMA
Authors: NISHIMURA DY ALWARD WLM BECK G HOCKEY R PATIL S STONE EM SHEFFIELD VC
Citation: Dy. Nishimura et al., CHARACTERIZATION OF 6P25 CHROMOSOMAL-ANOMALIES IN 2 PATIENTS IDENTIFIES A POTENTIAL CANDIDATE GENE CAUSING CONGENITAL GLAUCOMA, American journal of human genetics, 61(4), 1997, pp. 103-103
AN EFFICIENT METHOD FOR EVALUATING THE PREVALENCE OF SINGLE-BASE POLYMORPHISMS MUTATIONS IN CONTROL OR TEST POPULATIONS USING ARMS/
Authors: KANIS AB LOVE T NISHIMURA D STONE EM SHEFFIELD VC
Citation: Ab. Kanis et al., AN EFFICIENT METHOD FOR EVALUATING THE PREVALENCE OF SINGLE-BASE POLYMORPHISMS MUTATIONS IN CONTROL OR TEST POPULATIONS USING ARMS/, American journal of human genetics, 61(4), 1997, pp. 1285-1285
Risultati: 1-25 | 26-50 | 51-75 | 76-100 | >>