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Results: 1-17 |
Results: 17
THE GENOMIC ORGANIZATION OF THE MURINE PAX-8 GENE AND CHARACTERIZATION OF ITS BASAL PROMOTER
Authors: OKLADNOVA O POLEEV A FANTES J LEE M PLACHOV D HORST J
Citation: O. Okladnova et al., THE GENOMIC ORGANIZATION OF THE MURINE PAX-8 GENE AND CHARACTERIZATION OF ITS BASAL PROMOTER, Genomics, 42(3), 1997, pp. 452-461
THE RETICULOCALBIN GENE MAPS TO THE WAGR REGION IN HUMAN AND TO THE SMALL EYE HARWELL DELETION IN MOUSE
Authors: KENT J LEE M SCHEDL A BOYLE S FANTES J POWELL M RUSHMERE N ABBOTT C VANHEYNINGEN V BICKMORE WA
Citation: J. Kent et al., THE RETICULOCALBIN GENE MAPS TO THE WAGR REGION IN HUMAN AND TO THE SMALL EYE HARWELL DELETION IN MOUSE, Genomics, 42(2), 1997, pp. 260-267
MOLECULAR-GENETICS OF THE HUMAN GLUCOKINASE REGULATOR-FRUCTOKINASE (GCKR-KHK) REGION OF CHROMOSOME 2P23
Authors: HAYWARD BE WARNER JP DUNLOP N FANTES J INTODY S LEEK J MARKHAM AF BONTHRON DT
Citation: Be. Hayward et al., MOLECULAR-GENETICS OF THE HUMAN GLUCOKINASE REGULATOR-FRUCTOKINASE (GCKR-KHK) REGION OF CHROMOSOME 2P23, Biochemical Society transactions, 25(1), 1997, pp. 140-145
A FISH APPROACH TO DEFINING THE EXTENT AND POSSIBLE CLINICAL-SIGNIFICANCE OF DELETIONS AT THE WAGR LOCUS
Authors: CROLLA JA CAWDERY JE OLEY CA YOUNG ID GRAY J FANTES J VANHEYNINGEN V
Citation: Ja. Crolla et al., A FISH APPROACH TO DEFINING THE EXTENT AND POSSIBLE CLINICAL-SIGNIFICANCE OF DELETIONS AT THE WAGR LOCUS, Journal of Medical Genetics, 34(3), 1997, pp. 207-212
IDENTIFICATION OF A LARGE DUPLICATED GENE-CLUSTER REGION AT THE COMMON DELETION BREAKPOINTS OF PRADER-WILLI AND ANGELMAN-SYNDROMES
Authors: CHRISTIAN SL MARTIN SA FANTES J BHATT NK HUANG B LEDBETTER DH
Citation: Sl. Christian et al., IDENTIFICATION OF A LARGE DUPLICATED GENE-CLUSTER REGION AT THE COMMON DELETION BREAKPOINTS OF PRADER-WILLI AND ANGELMAN-SYNDROMES, American journal of human genetics, 61(4), 1997, pp. 24-24
CPG ISLANDS OF CHICKEN ARE CONCENTRATED ON MICROCHROMOSOMES
Authors: MCQUEEN HA FANTES J CROSS SH CLARK VH ARCHIBALD AL BIRD AP
Citation: Ha. Mcqueen et al., CPG ISLANDS OF CHICKEN ARE CONCENTRATED ON MICROCHROMOSOMES, Nature genetics, 12(3), 1996, pp. 321-324
CHROMOSOMAL LOCALIZATION IN MOUSE AND HUMAN OF THE VASOACTIVE-INTESTINAL-PEPTIDE RECEPTOR-TYPE-2 GENE - A POSSIBLE CONTRIBUTOR TO THE HOLOPROSENCEPHALY-3 PHENOTYPE
Authors: MACKAY M FANTES J SCHERER S BOYLE S WEST K TSUI LC BELLONI E LUTZ E VANHEYNINGEN V HARMAR AJ
Citation: M. Mackay et al., CHROMOSOMAL LOCALIZATION IN MOUSE AND HUMAN OF THE VASOACTIVE-INTESTINAL-PEPTIDE RECEPTOR-TYPE-2 GENE - A POSSIBLE CONTRIBUTOR TO THE HOLOPROSENCEPHALY-3 PHENOTYPE, Genomics, 37(3), 1996, pp. 345-353
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
LACK OF X INACTIVATION ASSOCIATED WITH MATERNAL X ISODISOMY - EVIDENCE FOR A COUNTING MECHANISM PRIOR TO X INACTIVATION DURING HUMAN EMBRYOGENESIS
Authors: MIGEON BR JEPPESEN P TORCHIA BS FU SD DUNN MA AXELMAN J SCHMECKPEPER BJ FANTES J ZORI RT DRISCOLL DJ
Citation: Br. Migeon et al., LACK OF X INACTIVATION ASSOCIATED WITH MATERNAL X ISODISOMY - EVIDENCE FOR A COUNTING MECHANISM PRIOR TO X INACTIVATION DURING HUMAN EMBRYOGENESIS, American journal of human genetics, 58(1), 1996, pp. 161-170
ANIRIDIA-ASSOCIATED CYTOGENETIC REARRANGEMENTS SUGGEST THAT A POSITION EFFECT MAY CAUSE THE MUTANT PHENOTYPE
Authors: FANTES J REDEKER B BREEN M BOYLE S BROWN J FLETCHER J JONES S BICKMORE W FUKUSHIMA Y MANNENS M DANES S VANHEYNINGEN V HANSON I
Citation: J. Fantes et al., ANIRIDIA-ASSOCIATED CYTOGENETIC REARRANGEMENTS SUGGEST THAT A POSITION EFFECT MAY CAUSE THE MUTANT PHENOTYPE, Human molecular genetics, 4(3), 1995, pp. 415-422
DIRECT MICRODISSECTION AND MICROCLONING OF A TRANSLOCATION BREAKPOINTREGION, T(1-11) (Q42.2-Q21), ASSOCIATED WITH SCHIZOPHRENIA
Authors: MUIR WJ GOSDEN CM BROOKES AJ FANTES J EVANS KL MAGUIRE SM STEVENSON B BOYLE S BLACKWOOD DHR STCLAIR DM PORTEOUS DJ WEITH A
Citation: Wj. Muir et al., DIRECT MICRODISSECTION AND MICROCLONING OF A TRANSLOCATION BREAKPOINTREGION, T(1-11) (Q42.2-Q21), ASSOCIATED WITH SCHIZOPHRENIA, Cytogenetics and cell genetics, 70(1-2), 1995, pp. 35-40
CHROMOSOME PAINTING OF RADIATION-INDUCED MICRONUCLEI
Authors: SLAVOTINEK AM THOMSON EJ FANTES J TAYLOR GM VANHEYNINGEN V NUSSE M
Citation: Am. Slavotinek et al., CHROMOSOME PAINTING OF RADIATION-INDUCED MICRONUCLEI, Journal of Medical Genetics, 32(2), 1995, pp. 139-139
ORGANIZATION OF MAMMALIAN CHROMOSOMES - INTEGRATION OF STRUCTURE AND FUNCTION
Authors: BICKMORE W CRAIG J FANTES J VANHEYNINGEN V
Citation: W. Bickmore et al., ORGANIZATION OF MAMMALIAN CHROMOSOMES - INTEGRATION OF STRUCTURE AND FUNCTION, Journal of cellular biochemistry, 1994, pp. 97-97
DE-NOVO 14Q32 MICRODELETION ON AN INHERITED T(1421) ROBERTSONIAN TRANSLOCATION RESULTING IN MULTIPLE CONGENITAL-ABNORMALITIES IN AN APPARENTLY BALANCED TRANSLOCATION CARRIER
Authors: BONTHRON DT SMITH SJL FANTES J GOSDEN CM
Citation: Dt. Bonthron et al., DE-NOVO 14Q32 MICRODELETION ON AN INHERITED T(1421) ROBERTSONIAN TRANSLOCATION RESULTING IN MULTIPLE CONGENITAL-ABNORMALITIES IN AN APPARENTLY BALANCED TRANSLOCATION CARRIER, Journal of Medical Genetics, 31(2), 1994, pp. 169-169
TRISOMY-12 IN B-CELL CHRONIC LYMPHOCYTIC-LEUKEMIA - ASSESSMENT OF LINEAGE RESTRICTION BY SIMULTANEOUS ANALYSIS OF IMMUNOPHENOTYPE AND GENOTYPE IN INTERPHASE CELLS BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: GARCIAMARCO J MATUTES E MORILLA R ELLIS J OSCIER D FANTES J CATOVSKY D PRICE CM
Citation: J. Garciamarco et al., TRISOMY-12 IN B-CELL CHRONIC LYMPHOCYTIC-LEUKEMIA - ASSESSMENT OF LINEAGE RESTRICTION BY SIMULTANEOUS ANALYSIS OF IMMUNOPHENOTYPE AND GENOTYPE IN INTERPHASE CELLS BY FLUORESCENCE IN-SITU HYBRIDIZATION, British Journal of Haematology, 87(1), 1994, pp. 44-50
MICRODISSECTION AND MICROCLONING OF THE TRANSLOCATION BREAKPOINT T(1-11)(Q42.2-Q21) ASSOCIATED WITH MAJOR MENTAL-ILLNESS
Authors: MUIR W WEITH A STCLAIR D BLACKWOOD D PORTEOUS D MAGUIRE S EVANS K BROOKES A BOYLE S VANHEYNINGEN V FANTES J GOSDEN C
Citation: W. Muir et al., MICRODISSECTION AND MICROCLONING OF THE TRANSLOCATION BREAKPOINT T(1-11)(Q42.2-Q21) ASSOCIATED WITH MAJOR MENTAL-ILLNESS, American journal of human genetics, 53(3), 1993, pp. 1744-1744
DE-NOVO MICRODELETION ON AN INHERITED ROBERTSONIAN TRANSLOCATION CHROMOSOME - A CAUSE FOR DYSMORPHISM IN THE APPARENTLY BALANCED TRANSLOCATION CARRIER
Authors: BONTHRON DT SMITH SJL FANTES J GOSDEN CM
Citation: Dt. Bonthron et al., DE-NOVO MICRODELETION ON AN INHERITED ROBERTSONIAN TRANSLOCATION CHROMOSOME - A CAUSE FOR DYSMORPHISM IN THE APPARENTLY BALANCED TRANSLOCATION CARRIER, American journal of human genetics, 53(3), 1993, pp. 629-637
Risultati: 1-17 |