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Results: 1-17 |
Results: 17
SPECTRUM OF CLINICAL FEATURES ASSOCIATED WITH INTERSTITIAL CHROMOSOME22Q11 DELETIONS
Authors: DIROCCO M BUOCOMPAGNI A PICCO P VIGNOLA S BORRONE C GIMELLI G
Citation: M. Dirocco et al., SPECTRUM OF CLINICAL FEATURES ASSOCIATED WITH INTERSTITIAL CHROMOSOME22Q11 DELETIONS, Journal of Medical Genetics, 35(4), 1998, pp. 346-346
MOLECULAR ANALYSIS OF 9P DELETIONS ASSOCIATED WITH XY SEX REVERSAL - REFINING THE LOCALIZATION OF A SEX-DETERMINING GENE TO THE TIP OF THE CHROMOSOME
Authors: GUIOLI S SCHMITT K CRITCHER R BOUZYK M SPURR NK OGATA T HOO JJ PINSKY L GIMELLI G PASZTOR L GOODFELLOW PN
Citation: S. Guioli et al., MOLECULAR ANALYSIS OF 9P DELETIONS ASSOCIATED WITH XY SEX REVERSAL - REFINING THE LOCALIZATION OF A SEX-DETERMINING GENE TO THE TIP OF THE CHROMOSOME, American journal of human genetics, 63(3), 1998, pp. 905-908
IMMUNOLOCALIZATION OF CENP-A SUGGESTS A DISTINCT NUCLEOSOME STRUCTUREAT THE INNER KINETOCHORE PLATE OF ACTIVE CENTROMERES
Authors: WARBURTON PE COOKE CA BOURASSA S VAFA O SULLIVAN BA STETTEN G GIMELLI G WARBURTON D TYLERSMITH C SULLIVAN KF POIRIER GG EARNSHAW WC
Citation: Pe. Warburton et al., IMMUNOLOCALIZATION OF CENP-A SUGGESTS A DISTINCT NUCLEOSOME STRUCTUREAT THE INNER KINETOCHORE PLATE OF ACTIVE CENTROMERES, Current biology, 7(11), 1997, pp. 901-904
THE PHENOTYPE OF A 45,X MALE WITH A Y 18 TRANSLOCATION/
Authors: GIMELLI G CINTI R VARONE P NASELLI A DIBATTISTA E PEZZOLO A
Citation: G. Gimelli et al., THE PHENOTYPE OF A 45,X MALE WITH A Y 18 TRANSLOCATION/, Clinical genetics, 49(1), 1996, pp. 37-41
THE SAME MOLECULAR MECHANISM AT THE MATERNAL MEIOSIS-I PRODUCES MONOCENTRIC AND DICENTRIC 8P DUPLICATIONS
Authors: FLORIDIA G PIANTANIDA M MINELLI A DELLAVECCHIA C BONAGLIA C ROSSI E GIMELLI G CROCI G FRANCHI F GILGENKRANTZ S GRAMMATICO P DALPRA L WOOD S DANESINO C ZUFFARDI O
Citation: G. Floridia et al., THE SAME MOLECULAR MECHANISM AT THE MATERNAL MEIOSIS-I PRODUCES MONOCENTRIC AND DICENTRIC 8P DUPLICATIONS, American journal of human genetics, 58(4), 1996, pp. 785-796
A NEW BIALLELIC DNA POLYMORPHISM OF THE HUMAN COL5A1 GENE
Authors: CAPPA F CARIDI G GIMELLI G GHIGGERI GM
Citation: F. Cappa et al., A NEW BIALLELIC DNA POLYMORPHISM OF THE HUMAN COL5A1 GENE, Human genetics, 95(5), 1995, pp. 599-600
DEFINITIVE ASSIGNMENT OF THE GROWTH HORMONE-RELEASING FACTOR GENE TO 20Q11.2
Authors: PEZZOLO A GIMELLI G SPOSITO M GIUSSANI U ROSSI E ZUFFARDI O
Citation: A. Pezzolo et al., DEFINITIVE ASSIGNMENT OF THE GROWTH HORMONE-RELEASING FACTOR GENE TO 20Q11.2, Human genetics, 93(2), 1994, pp. 213-214
GENOTYPIC, PHENOTYPIC AND BIOLOGICAL CHARACTERIZATION OF A NOVEL HUMAN LUNG ADENOCARCINOMA CELL-LINE (LC-89)
Authors: PAGANUZZI M MARRONI P PEZZOLO A GIMELLI G CAVALLO F DIPIERRO F DEANGELIS P FORNI G GROSSI CE
Citation: M. Paganuzzi et al., GENOTYPIC, PHENOTYPIC AND BIOLOGICAL CHARACTERIZATION OF A NOVEL HUMAN LUNG ADENOCARCINOMA CELL-LINE (LC-89), Oncology, 51(3), 1994, pp. 220-225
A NOVEL HUMAN LUNG ADENOCARCINOMA CELL-LINE (LC89)
Authors: PAGANUZZI M MARRONI P ZANNINI C PEZZOLO A GIMELLI G CAVALLO F VERZOLA D DEANGELIS P FORNI G GROSSI CE
Citation: M. Paganuzzi et al., A NOVEL HUMAN LUNG ADENOCARCINOMA CELL-LINE (LC89), Cancer detection and prevention, 17(2), 1993, pp. 343-343
PRESENCE OF TELOMERIC AND SUBTELOMERIC SEQUENCES AT THE FUSION POINTSOF RING CHROMOSOMES INDICATES THAT THE RING SYNDROME IS CAUSED BY RING INSTABILITY
Authors: PEZZOLO A GIMELLI G COHEN A LAVAGGETTO A ROMANO C FOGU G ZUFFARDI O
Citation: A. Pezzolo et al., PRESENCE OF TELOMERIC AND SUBTELOMERIC SEQUENCES AT THE FUSION POINTSOF RING CHROMOSOMES INDICATES THAT THE RING SYNDROME IS CAUSED BY RING INSTABILITY, Human genetics, 92(1), 1993, pp. 23-27
ICF SYNDROME WITH VARIABLE EXPRESSION IN SIBS
Authors: GIMELLI G VARONE P PEZZOLO A LERONE M PISTOIA V
Citation: G. Gimelli et al., ICF SYNDROME WITH VARIABLE EXPRESSION IN SIBS, Journal of Medical Genetics, 30(5), 1993, pp. 429-432
IDENTIFICATION OF RING Y-CHROMOSOME - CYTOGENETIC ANALYSIS, SOUTHERN BLOT AND FLUORESCENT IN-SITU HYBRIDIZATION
Authors: PEZZOLO A PERRONI L GIMELLI G ARSLANIAN A PORTA S GANDULLIA P GANDULLIA E
Citation: A. Pezzolo et al., IDENTIFICATION OF RING Y-CHROMOSOME - CYTOGENETIC ANALYSIS, SOUTHERN BLOT AND FLUORESCENT IN-SITU HYBRIDIZATION, Annales de genetique, 36(2), 1993, pp. 121-125
A NEW CASE OF SUBMICROSCOPIC 4P16.3 DE-NOVO DELETION (WOLF-HIRSCHHORNSYNDROME) IDENTIFIED BY FLUORESCENCE IN-SITU HYBRIDIZATION
Authors: CONCOLINO D PEZZOLO A SPERLI D GIMELLI G STRISCIUGLIO P
Citation: D. Concolino et al., A NEW CASE OF SUBMICROSCOPIC 4P16.3 DE-NOVO DELETION (WOLF-HIRSCHHORNSYNDROME) IDENTIFIED BY FLUORESCENCE IN-SITU HYBRIDIZATION, American journal of human genetics, 53(3), 1993, pp. 1565-1565
DIFFERENCES IN THE PATTERN OF BASIC FGF AND FGF RECEPTOR (FLG) IMMUNOREACTIVITY IN THE NORMAL HUMAN EYE
Authors: GIMELLI G MAHER P BAIRD A HANNEKEN A
Citation: G. Gimelli et al., DIFFERENCES IN THE PATTERN OF BASIC FGF AND FGF RECEPTOR (FLG) IMMUNOREACTIVITY IN THE NORMAL HUMAN EYE, Investigative ophthalmology & visual science, 33(4), 1992, pp. 820-820
DEVELOPMENTAL-CHANGES IN FGF RECEPTOR (FLG) IMMUNOREACTIVITY IN THE RCS RAT RETINA
Authors: NURSE L GIMELLI G BAIRD A HANNEKEN A
Citation: L. Nurse et al., DEVELOPMENTAL-CHANGES IN FGF RECEPTOR (FLG) IMMUNOREACTIVITY IN THE RCS RAT RETINA, Investigative ophthalmology & visual science, 33(4), 1992, pp. 822-822
HIGH-AFFINITY FGF RECEPTOR (FLG) IMMUNOREACTIVITY ON VASCULAR ENDOTHELIAL-CELLS
Authors: HANNEKEN A GIMELLI G BAIRD A
Citation: A. Hanneken et al., HIGH-AFFINITY FGF RECEPTOR (FLG) IMMUNOREACTIVITY ON VASCULAR ENDOTHELIAL-CELLS, Investigative ophthalmology & visual science, 33(4), 1992, pp. 1089-1089
COMPARATIVE ANTERIOR SEGMENT LOCALIZATION OF MONOCLONAL-ANTIBODIES 454A12 AND 260F9 IN THE HUMAN EYE
Authors: AVALLONE J FULCHER S HANNEKEN A GIMELLI G SUTPHIN J HOUSTON LL FOULKS G
Citation: J. Avallone et al., COMPARATIVE ANTERIOR SEGMENT LOCALIZATION OF MONOCLONAL-ANTIBODIES 454A12 AND 260F9 IN THE HUMAN EYE, Investigative ophthalmology & visual science, 33(4), 1992, pp. 1237-1237
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