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Results: 1-13 |
Results: 13
PRENATAL-DIAGNOSIS OF TRISOMY-21 AND TRIPLOIDY BY ANALYSIS OF FETAL CELLS IN MATERNAL BLOOD
Authors: PEZZOLO A SANTI F PISTOIA V DEBIASIO P
Citation: A. Pezzolo et al., PRENATAL-DIAGNOSIS OF TRISOMY-21 AND TRIPLOIDY BY ANALYSIS OF FETAL CELLS IN MATERNAL BLOOD, Cytogenetics and cell genetics, 77(1-2), 1997, pp. 176-176
PRENATAL-DIAGNOSIS OF TRIPLOIDY USING FETAL CELLS IN THE MATERNAL CIRCULATION
Authors: PEZZOLO A SANTI F PISTOIA V DEBIASIO P
Citation: A. Pezzolo et al., PRENATAL-DIAGNOSIS OF TRIPLOIDY USING FETAL CELLS IN THE MATERNAL CIRCULATION, Prenatal diagnosis, 17(4), 1997, pp. 389-389
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
MOLECULAR ANALYSIS IN PATIENTS WITH PRADE R-WILLI AND ANGELMAN SYNDROMES
Authors: CARROZZO R TONLORENZI R MAZZOTTI R PEZZOLO A CINTI R GATTI R
Citation: R. Carrozzo et al., MOLECULAR ANALYSIS IN PATIENTS WITH PRADE R-WILLI AND ANGELMAN SYNDROMES, Rivista italiana di pediatria, 20(6), 1994, pp. 677-682
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
MATERNAL DERIVATION OF INV-DUP(22) AND CLINICAL VARIATION IN CAT-EYE-SYNDROME
Authors: TUPLER R HOELLER A PEZZOLO A MARASCHIO P
Citation: R. Tupler et al., MATERNAL DERIVATION OF INV-DUP(22) AND CLINICAL VARIATION IN CAT-EYE-SYNDROME, Annales de genetique, 37(3), 1994, pp. 153-155
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
CYTOGENETICS OF MULTIPLE ENDOCRINE NEOPLASIA SYNDROMES .3. ANALYSIS OF AN INSULINOMA FROM A SUBJECT WITH MEN-1 BY CHROMOSOME PAINTING
Authors: MARASCHIO P PEZZOLO A BRANDI ML CORTINOVIS M DAINOTTI E SCAPPATICCI S FRACCARO M
Citation: P. Maraschio et al., CYTOGENETICS OF MULTIPLE ENDOCRINE NEOPLASIA SYNDROMES .3. ANALYSIS OF AN INSULINOMA FROM A SUBJECT WITH MEN-1 BY CHROMOSOME PAINTING, Cancer genetics and cytogenetics, 70(1), 1993, pp. 68-70
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
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