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Results: 1-25 | 26-50 | 51-56
Results: 26-50/56
ASSOCIATION OF A CHROMOSOME DELETION SYNDROME WITH A FRAGILE SITE WITHIN THE PROTOONCOGENE CBL2
Authors: JONES C PENNY L MATTINA T YU S BAKER E VOULLAIRE L LANGDON WY SUTHERLAND GR RICHARDS RI TUNNACLIFFE A
Citation: C. Jones et al., ASSOCIATION OF A CHROMOSOME DELETION SYNDROME WITH A FRAGILE SITE WITHIN THE PROTOONCOGENE CBL2, Nature, 376(6536), 1995, pp. 145-149
SIMPLE TANDEM DNA REPEATS AND HUMAN GENETIC-DISEASE
Authors: SUTHERLAND GR RICHARDS RI
Citation: Gr. Sutherland et Ri. Richards, SIMPLE TANDEM DNA REPEATS AND HUMAN GENETIC-DISEASE, Proceedings of the National Academy of Sciences of the United Statesof America, 92(9), 1995, pp. 3636-3641
FRAXE AND MENTAL-RETARDATION
Authors: MULLEY JC YU S LOESCH DZ HAY DA DONNELLY A GEDEON AK CARBONELL P LOPEZ I GLOVER G GABARRON I YU PWL BAKER E HAAN EA HOCKEY A KNIGHT SJL DAVIES KE RICHARDS RI SUTHERLAND GR
Citation: Jc. Mulley et al., FRAXE AND MENTAL-RETARDATION, Journal of Medical Genetics, 32(3), 1995, pp. 162-169
A HIGHLY INTEGRATED MAP OF HUMAN-CHROMOSOME-16
Authors: DOGGETT NA CALLEN DF GOODWIN LA TESMER JG MEINCKE LJ BRUCE DC ALTHERR MR FORD AA TORNEY DC SUTHERLAND RD LOWENSTEIN MG MUNDT MO BRUNO WJ KNILL EH DEAVEN LL SUTHERLAND GR RICHARDS RI MOYZIS RK
Citation: Na. Doggett et al., A HIGHLY INTEGRATED MAP OF HUMAN-CHROMOSOME-16, American journal of human genetics, 57(4), 1995, pp. 72-72
THE FRAGILE SITE FRA11B IS LOCATED WITHIN THE PROTOONCOGENE CBL2 AND IS ASSOCIATED WITH A CHROMOSOME DELETION SYNDROME
Authors: JONES C PENNY L MATTINA T YU S BAKER E VOULLAIRE L LANGDON WY SUTHERLAND GR RICHARDS RI TUNNACLIFFE A
Citation: C. Jones et al., THE FRAGILE SITE FRA11B IS LOCATED WITHIN THE PROTOONCOGENE CBL2 AND IS ASSOCIATED WITH A CHROMOSOME DELETION SYNDROME, American journal of human genetics, 57(4), 1995, pp. 85-85
PHYSICAL AND TRANSCRIPTIONAL MAP OF THE FMF CANDIDATE REGION
Authors: AKSENTIJEVICH I ALTHERR M APOSTOLOU S BALOW JE BLAKE T CALLEN DF CENTOLA M CHEN X CHEN X COLLINS FS DOGGETT NA FISCHELGHODSIAN N GARDNER D GUMUCIO D KRIZMAN DB LEVY E LIU P MARRONE BL PRAS E PRAS M RICHARDS RI ROTTER JI SHELTON D SHOHAT M SOOD R WOOD G KASTNER DL
Citation: I. Aksentijevich et al., PHYSICAL AND TRANSCRIPTIONAL MAP OF THE FMF CANDIDATE REGION, American journal of human genetics, 57(4), 1995, pp. 1479-1479
FRAXAC2 INSTABILITY
Authors: RICHARDS RI HOLMAN K FRIEND K STAPLES A SUTHERLAND GR OUDET C BIANCALANA V MANDEL JL
Citation: Ri. Richards et al., FRAXAC2 INSTABILITY, Nature genetics, 7(2), 1994, pp. 122-122
SIMPLE REPEAT DNA IS NOT REPLICATED SIMPLY
Authors: RICHARDS RI SUTHERLAND GR
Citation: Ri. Richards et Gr. Sutherland, SIMPLE REPEAT DNA IS NOT REPLICATED SIMPLY, Nature genetics, 6(2), 1994, pp. 114-116
PHYSICAL LINKAGE OF THE FRAGILE SITE FRA11B AND A JACOBSEN SYNDROME CHROMOSOME DELETION BREAKPOINT IN 11Q23.3
Authors: JONES C SLIJEPCEVIC P MARSH S BAKER E LANGDON WY RICHARDS RI TUNNACLIFFE A
Citation: C. Jones et al., PHYSICAL LINKAGE OF THE FRAGILE SITE FRA11B AND A JACOBSEN SYNDROME CHROMOSOME DELETION BREAKPOINT IN 11Q23.3, Human molecular genetics, 3(12), 1994, pp. 2123-2130
DINUCLEOTIDE REPEAT POLYMORPHISMS AT THE D16S525, D16S359, D16S531 AND D16S522 LOCI
Authors: SHEN Y HOLMAN K DOGGETT NA CALLEN DF SUTHERLAND GR RICHARDS RI
Citation: Y. Shen et al., DINUCLEOTIDE REPEAT POLYMORPHISMS AT THE D16S525, D16S359, D16S531 AND D16S522 LOCI, Human molecular genetics, 3(1), 1994, pp. 210-210
A PCR-BASED GENETIC-LINKAGE MAP OF HUMAN-CHROMOSOME-16
Authors: SHEN Y KOZMAN HM THOMPSON A PHILLIPS HA HOLMAN K NANCARROW J LANE S CHEN LZ APOSTOLOU S DOGGETT NA CALLEN DF MULLEY JC SUTHERLAND GR RICHARDS RI
Citation: Y. Shen et al., A PCR-BASED GENETIC-LINKAGE MAP OF HUMAN-CHROMOSOME-16, Genomics, 22(1), 1994, pp. 68-76
A LINKAGE MAP OF MICROSATELLITE MARKERS ON THE HUMAN X-CHROMOSOME
Authors: DONNELLY A KOZMAN H GEDEON AK WEBB S LYNCH M SUTHERLAND GR RICHARDS RI MULLEY JC
Citation: A. Donnelly et al., A LINKAGE MAP OF MICROSATELLITE MARKERS ON THE HUMAN X-CHROMOSOME, Genomics, 20(3), 1994, pp. 363-370
ISOLATION AND CHARACTERIZATION OF TRANSCRIBED SEQUENCES FROM A CHROMOSOME-16 HN-CDNA LIBRARY AND THE PHYSICAL MAPPING OF GENES AND TRANSCRIBED SEQUENCES USING A HIGH-RESOLUTION SOMATIC-CELL PANEL OF HUMAN CHROMOSOME-16
Authors: WHITMORE SA APOSTOLOU S LANE S NANCARROW JK PHILLIPS HA RICHARDS RI SUTHERLAND GR CALLEN DF
Citation: Sa. Whitmore et al., ISOLATION AND CHARACTERIZATION OF TRANSCRIBED SEQUENCES FROM A CHROMOSOME-16 HN-CDNA LIBRARY AND THE PHYSICAL MAPPING OF GENES AND TRANSCRIBED SEQUENCES USING A HIGH-RESOLUTION SOMATIC-CELL PANEL OF HUMAN CHROMOSOME-16, Genomics, 20(2), 1994, pp. 169-175
SIXTH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION
Authors: SUTHERLAND GR BROWN WT HAGERMAN R JENKINS E LUBS H MANDEL JL NELSON D NERI G PARTINGTON MW RICHARDS RI STEVENSON R TURNER G
Citation: Gr. Sutherland et al., SIXTH INTERNATIONAL WORKSHOP ON THE FRAGILE-X AND X-LINKED MENTAL-RETARDATION, American journal of medical genetics, 51(4), 1994, pp. 281-293
IMPLICATIONS OF FRA16A STRUCTURE FOR THE MECHANISM OF CHROMOSOMAL FRAGILE SITE GENESIS
Authors: NANCARROW JK KREMER E HOLMAN K EYRE H DOGGETT NA LEPASLIER D CALLEN DF SUTHERLAND GR RICHARDS RI
Citation: Jk. Nancarrow et al., IMPLICATIONS OF FRA16A STRUCTURE FOR THE MECHANISM OF CHROMOSOMAL FRAGILE SITE GENESIS, Science, 264(5167), 1994, pp. 1938-1941
DNA REPEATS - A TREASURY OF HUMAN VARIATION
Authors: SUTHERLAND GR RICHARDS RI
Citation: Gr. Sutherland et Ri. Richards, DNA REPEATS - A TREASURY OF HUMAN VARIATION, The New England journal of medicine, 331(3), 1994, pp. 191-193
DYNAMIC MUTATIONS
Authors: SUTHERLAND GR RICHARDS RI
Citation: Gr. Sutherland et Ri. Richards, DYNAMIC MUTATIONS, American scientist, 82(2), 1994, pp. 157-163
FRAGILE-X SYNDROME UNSTABLE ELEMENT, P(CCG)N, AND OTHER SIMPLE TANDEMREPEAT SEQUENCES ARE BINDING-SITES FOR SPECIFIC NUCLEAR PROTEINS
Authors: RICHARDS RI HOLMAN K YU S SUTHERLAND GR
Citation: Ri. Richards et al., FRAGILE-X SYNDROME UNSTABLE ELEMENT, P(CCG)N, AND OTHER SIMPLE TANDEMREPEAT SEQUENCES ARE BINDING-SITES FOR SPECIFIC NUCLEAR PROTEINS, Human molecular genetics, 2(9), 1993, pp. 1429-1435
5 DINUCLEOTIDE REPEAT POLYMORPHISMS ON HUMAN CHROMOSOME-16Q24.2-Q24.3
Authors: SHEN Y HOLMAN K DOGGETT NA CALLEN DF SUTHERLAND GR RICHARDS RI
Citation: Y. Shen et al., 5 DINUCLEOTIDE REPEAT POLYMORPHISMS ON HUMAN CHROMOSOME-16Q24.2-Q24.3, Human molecular genetics, 2(9), 1993, pp. 1504-1504
6 DINUCLEOTIDE REPEAT POLYMORPHISMS ON HUMAN CHROMOSOME-16Q12.1-Q24.1
Authors: SHEN Y HOLMAN K DOGGETT NA CALLEN DF SUTHERLAND GR RICHARDS RI
Citation: Y. Shen et al., 6 DINUCLEOTIDE REPEAT POLYMORPHISMS ON HUMAN CHROMOSOME-16Q12.1-Q24.1, Human molecular genetics, 2(9), 1993, pp. 1505-1505
3 DINUCLEOTIDE REPEAT POLYMORPHISMS ON HUMAN CHROMOSOME-16P13.11-P13.3
Authors: SHEN Y HOLMAN K DOGGETT NA CALLEN DF SUTHERLAND GR RICHARDS RI
Citation: Y. Shen et al., 3 DINUCLEOTIDE REPEAT POLYMORPHISMS ON HUMAN CHROMOSOME-16P13.11-P13.3, Human molecular genetics, 2(9), 1993, pp. 1506-1506
4 DINUCLEOTIDE REPEAT POLYMORPHISMS ON HUMAN CHROMOSOME-16
Authors: SHEN Y HOLMAN K DOGGETT NA CALLEN DF SUTHERLAND GR RICHARDS RI
Citation: Y. Shen et al., 4 DINUCLEOTIDE REPEAT POLYMORPHISMS ON HUMAN CHROMOSOME-16, Human molecular genetics, 2(10), 1993, pp. 1745-1745
FINE GENETIC-MAPPING OF THE BATTEN DISEASE LOCUS (CLN3) BY HAPLOTYPE ANALYSIS AND DEMONSTRATION OF ALLELIC ASSOCIATION WITH CHROMOSOME-16P MICROSATELLITE LOCI
Authors: MITCHISON HM THOMPSON AD MULLEY JC KOZMAN HM RICHARDS RI CALLEN DF STALLINGS RL DOGGETT NA ATTWOOD J MCKAY TR SUTHERLAND GR GARDINER RM
Citation: Hm. Mitchison et al., FINE GENETIC-MAPPING OF THE BATTEN DISEASE LOCUS (CLN3) BY HAPLOTYPE ANALYSIS AND DEMONSTRATION OF ALLELIC ASSOCIATION WITH CHROMOSOME-16P MICROSATELLITE LOCI, Genomics, 16(2), 1993, pp. 455-460
A GENETIC-MAP OF MICROSATELLITE MARKERS ON THE X-CHROMOSOME
Authors: DONNELLY A KOZMAN H GEDEON AK WEBB S LYNCH M RICHARDS RI MULLEY JC
Citation: A. Donnelly et al., A GENETIC-MAP OF MICROSATELLITE MARKERS ON THE X-CHROMOSOME, Cytogenetics and cell genetics, 64(3-4), 1993, pp. 182-182
FRAGILE-X SYNDROME - THE MOST COMMON CAUSE OF FAMILIAL INTELLECTUAL HANDICAP
Authors: SUTHERLAND GR MULLEY JC RICHARDS RI
Citation: Gr. Sutherland et al., FRAGILE-X SYNDROME - THE MOST COMMON CAUSE OF FAMILIAL INTELLECTUAL HANDICAP, Medical journal of Australia, 158(7), 1993, pp. 482-485
Risultati: 1-25 | 26-50 | 51-56