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Results: 1-25 | 26-38 |
Results: 26-38/38
DIRECT SELECTION OF CDNAS USING WHOLE CHROMOSOMES
Authors: ROUQUIER S TRASK BJ TAVIAUX S VANDENENGH G DIRIONG S LENNON GG GIORGI D
Citation: S. Rouquier et al., DIRECT SELECTION OF CDNAS USING WHOLE CHROMOSOMES, Nucleic acids research, 23(21), 1995, pp. 4415-4420
MOLECULAR ANALYSIS OF A NOVEL SUBTELOMERIC REPEAT WITH POLYMORPHIC CHROMOSOMAL DISTRIBUTION
Authors: MARTINGALLARDO A LAMERDIN J SOPAPAN P FRIEDMAN C FERTITTA AL GARCIA E CARRANO A NEGOREV D MACINA RA TRASK BJ RIETHMAN HC
Citation: A. Martingallardo et al., MOLECULAR ANALYSIS OF A NOVEL SUBTELOMERIC REPEAT WITH POLYMORPHIC CHROMOSOMAL DISTRIBUTION, Cytogenetics and cell genetics, 71(3), 1995, pp. 289-295
SMITH-MAGENIS SYNDROME DELETION - A CASE WITH EQUIVOCAL CYTOGENETIC FINDINGS RESOLVED BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: JUYAL RC GREENBERG F MENGDEN GA LUPSKI JR TRASK BJ VANDENENGH G LINDSAY EA CHRISTY H CHEN KS BALDINI A SHAFFER LG PATEL PI
Citation: Rc. Juyal et al., SMITH-MAGENIS SYNDROME DELETION - A CASE WITH EQUIVOCAL CYTOGENETIC FINDINGS RESOLVED BY FLUORESCENCE IN-SITU HYBRIDIZATION, American journal of medical genetics, 58(3), 1995, pp. 286-291
EVIDENCE FOR THE ORGANIZATION OF CHROMATIN IN MEGABASE PAIR-SIZED LOOPS ARRANGED ALONG A RANDOM-WALK PATH IN THE HUMAN G0 G1 INTERPHASE NUCLEUS/
Authors: YOKOTA H VANDENENGH G HEARST JE SACHS RK TRASK BJ
Citation: H. Yokota et al., EVIDENCE FOR THE ORGANIZATION OF CHROMATIN IN MEGABASE PAIR-SIZED LOOPS ARRANGED ALONG A RANDOM-WALK PATH IN THE HUMAN G0 G1 INTERPHASE NUCLEUS/, The Journal of cell biology, 130(6), 1995, pp. 1239-1249
ASSIGNMENT OF THE HUMAN P27(KIP1) GENE TO 12P13 AND ITS ANALYSIS IN LEUKEMIAS
Authors: PIETENPOL JA BOHLANDER SK SATO Y PAPADOPOULOS N LIU B FRIEDMAN C TRASK BJ ROBERTS JM KINZLER KW ROWLEY JD VOGELSTEIN B
Citation: Ja. Pietenpol et al., ASSIGNMENT OF THE HUMAN P27(KIP1) GENE TO 12P13 AND ITS ANALYSIS IN LEUKEMIAS, Cancer research, 55(6), 1995, pp. 1206-1210
THE 18Q(-) SYNDROME - ANALYSIS OF CHROMOSOMES BY BIVARIATE FLOW KARYOTYPING AND THE PCR REVEALS A SUCCESSIVE SET OF DELETION BREAKPOINTS WITHIN 18Q21.2-Q22.2
Authors: SILVERMAN GA SCHNEIDER SS MASSA HF FLINT A LALANDE M LEONARD JC OVERHAUSER J VANDENENGH G TRASK BJ
Citation: Ga. Silverman et al., THE 18Q(-) SYNDROME - ANALYSIS OF CHROMOSOMES BY BIVARIATE FLOW KARYOTYPING AND THE PCR REVEALS A SUCCESSIVE SET OF DELETION BREAKPOINTS WITHIN 18Q21.2-Q22.2, American journal of human genetics, 56(4), 1995, pp. 926-937
INTEGRATION OF PHYSICAL, GENETIC AND CYTOGENETIC MAPS OF HUMAN-CHROMOSOME-7 - ISOLATION AND ANALYSIS OF YEAST ARTIFICIAL CHROMOSOME CLONES FOR 117 MAPPED GENETIC-MARKERS
Authors: GREEN ED IDOL JR MOHRTIDWELL RM BRADEN VV PELUSO DC FULTON RS MASSA HF MAGNESS CL WILSON AM KIMURA J WEISSENBACH J TRASK BJ
Citation: Ed. Green et al., INTEGRATION OF PHYSICAL, GENETIC AND CYTOGENETIC MAPS OF HUMAN-CHROMOSOME-7 - ISOLATION AND ANALYSIS OF YEAST ARTIFICIAL CHROMOSOME CLONES FOR 117 MAPPED GENETIC-MARKERS, Human molecular genetics, 3(3), 1994, pp. 489-501
CLONING, SEQUENCING, AND MAPPING OF THE HUMAN-CHROMOSOME-14 HEAT-SHOCK PROTEIN GENE (HSPA2)
Authors: BONNYCASTLE LLC YU CE HUNT CR TRASK BJ CLANCY KP WEBER JL PATTERSON D SCHELLENBERG GD
Citation: Llc. Bonnycastle et al., CLONING, SEQUENCING, AND MAPPING OF THE HUMAN-CHROMOSOME-14 HEAT-SHOCK PROTEIN GENE (HSPA2), Genomics, 23(1), 1994, pp. 85-93
TEL AND THE GENE FOR P27KIP1 ARE FREQUENTLY DEPLETED IN PATIENTS WITH12P13 REARRANGEMENTS AND HEMATOPOIETIC MALIGNANCIES
Authors: SATO Y SUTO Y PIETENPOL J GOLUB TR GILLILAND DG ROBERTS JM TRASK BJ LEBEAU MM VOGELSTEIN B ROWLEY JD BOHLANDER SK
Citation: Y. Sato et al., TEL AND THE GENE FOR P27KIP1 ARE FREQUENTLY DEPLETED IN PATIENTS WITH12P13 REARRANGEMENTS AND HEMATOPOIETIC MALIGNANCIES, Blood, 84(10), 1994, pp. 10000292-10000292
EVIDENCE FOR A RECESSIVE PMP22 POINT MUTATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE-1A
Authors: ROA BB GARCIA CA LIU PT KILLIAN JM TRASK BJ SUTER U SNIPES GJ ORTIZLOPEZ R SHOOTER EM PATEL PI LUPSKI JR
Citation: Bb. Roa et al., EVIDENCE FOR A RECESSIVE PMP22 POINT MUTATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE-1A, Nature genetics, 5(2), 1993, pp. 189-194
DISCORDANT PHENOTYPE OF 2 OVERLAPPING DELETIONS INVOLVING THE PAX3 GENE IN CHROMOSOME-2Q35
Authors: PASTERIS NG TRASK BJ SHELDON S GORSKI JL
Citation: Ng. Pasteris et al., DISCORDANT PHENOTYPE OF 2 OVERLAPPING DELETIONS INVOLVING THE PAX3 GENE IN CHROMOSOME-2Q35, Human molecular genetics, 2(7), 1993, pp. 953-959
STUDIES OF METAPHASE AND INTERPHASE CHROMOSOMES USING FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: TRASK BJ ALLEN S MASSA H FERTITTA A SACHS R VANDENENGH G WU M
Citation: Bj. Trask et al., STUDIES OF METAPHASE AND INTERPHASE CHROMOSOMES USING FLUORESCENCE IN-SITU HYBRIDIZATION, Cold Spring Harbor Symposia on Quantitative Biology, 58, 1993, pp. 767-775
EVIDENCE FOR A RECESSIVE POINT MUTATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE-1A
Authors: GARCIA CA ROA BB PENTAO L KILLIAN JM TRASK BJ SUTER U SNIPES GJ SHOOTER E PATEL PI LUPSKI JR
Citation: Ca. Garcia et al., EVIDENCE FOR A RECESSIVE POINT MUTATION IN CHARCOT-MARIE-TOOTH DISEASE TYPE-1A, American journal of human genetics, 53(3), 1993, pp. 1162-1162
Risultati: 1-25 | 26-38 |