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Results: 1-12 |
Results: 12
A NEW CANDIDATE REGION FOR THE POSITIONAL CLONING OF THE XLP GENE
Authors: BOLINO A YIN L SERI M CUSANO R CINTI R COFFEY A BROOKSBANK R HOWELL G BENTLEY D DAVIS JR LANYI A HUANG DL STARK M CREAVEN M BJORKHAUG L HEITZMANN F LAMARTINE J GAUDI S SYLLA BS LENOIR GM CASTAGNOLA E GIACCHINO R PORTA G FRANCO B ZOLLO M SUMEGI J ROMEO G
Citation: A. Bolino et al., A NEW CANDIDATE REGION FOR THE POSITIONAL CLONING OF THE XLP GENE, European journal of human genetics, 6(5), 1998, pp. 509-517
A CANDIDATE GENE APPROACH TO IDENTIFY MODIFIERS OF CYSTIC-FIBROSIS PHENOTYPE
Authors: ROMIO L MUSANTE L CINTI R SERI M GALIETTA LJV
Citation: L. Romio et al., A CANDIDATE GENE APPROACH TO IDENTIFY MODIFIERS OF CYSTIC-FIBROSIS PHENOTYPE, European journal of human genetics, 6, 1998, pp. 4259-4259
HIGH-RESOLUTION MAPPING OF THE X-LINKED LYMPHOPROLIFERATIVE SYNDROME REGION BY FISH ON COMBED DNA
Authors: MONIER K MICHALET X LAMARTINE J SCHURRA C HEITZMANN F YIN L CINTI R SYLLA BS CREAVEN M PORTA G VOURCH C ROBERTNICOUD M BENSIMON A ROMEO G
Citation: K. Monier et al., HIGH-RESOLUTION MAPPING OF THE X-LINKED LYMPHOPROLIFERATIVE SYNDROME REGION BY FISH ON COMBED DNA, Cytogenetics and cell genetics, 81(3-4), 1998, pp. 259-264
BRIEF CLINICAL REPORT - CENTRIC FISSION OF CHROMOSOME-9 IN A BOY WITHTRISOMY 9P
Authors: CONCOLINO D CINTI R MORICCA M ANDRIA G STRISCIUGLIO P
Citation: D. Concolino et al., BRIEF CLINICAL REPORT - CENTRIC FISSION OF CHROMOSOME-9 IN A BOY WITHTRISOMY 9P, American journal of medical genetics, 79(1), 1998, pp. 35-37
PARTIAL TRISOMY 1(Q42-]QTER) - A NEW CASE WITH A MILD PHENOTYPE
Authors: CONCOLINO D CINTI R FERRARO L MORICCA MT STRISCIUGLIO P
Citation: D. Concolino et al., PARTIAL TRISOMY 1(Q42-]QTER) - A NEW CASE WITH A MILD PHENOTYPE, Journal of Medical Genetics, 35(1), 1998, pp. 75-77
ASSIGNMENT OF MOUSE GFRA1, THE HOMOLOG OF A NEW HUMAN HSCR CANDIDATE GENE, TO THE TELOMERIC REGION OF MOUSE-CHROMOSOME-19
Authors: PULITI A CINTI R SERI M CECCHERINI I ROMEO G
Citation: A. Puliti et al., ASSIGNMENT OF MOUSE GFRA1, THE HOMOLOG OF A NEW HUMAN HSCR CANDIDATE GENE, TO THE TELOMERIC REGION OF MOUSE-CHROMOSOME-19, Cytogenetics and cell genetics, 78(3-4), 1997, pp. 291-294
MOLECULAR-CLONING AND MAPPING OF A HUMAN CDNA (PA2G4) THAT ENCODES A PROTEIN HIGHLY HOMOLOGOUS TO THE MOUSE-CELL CYCLE PROTEIN P38-2G4
Authors: LAMARTINE J SERI M CINTI R HEITZMANN F CREAVEN M RADOMSKI N JOST E LENOIR GM ROMEO G SYLLA BS
Citation: J. Lamartine et al., MOLECULAR-CLONING AND MAPPING OF A HUMAN CDNA (PA2G4) THAT ENCODES A PROTEIN HIGHLY HOMOLOGOUS TO THE MOUSE-CELL CYCLE PROTEIN P38-2G4, Cytogenetics and cell genetics, 78(1), 1997, pp. 31-35
CEREBRAL DEFECTS CONFIRM MIDLINE DEVELOPMENTAL FIELD DISTURBANCES IN SUPERNUMERARY DER(22), T(11-22) SYNDROME
Authors: PALLOTTA E FUSILLI P EHRESMANN T CINTI R VERROTTI A MORGESE G
Citation: E. Pallotta et al., CEREBRAL DEFECTS CONFIRM MIDLINE DEVELOPMENTAL FIELD DISTURBANCES IN SUPERNUMERARY DER(22), T(11-22) SYNDROME, Clinical genetics, 50(5), 1996, pp. 411-416
A MILD FORM OF ROBERTS SC PHOCOMELIA SYNDROME WITH ASYMMETRICAL REDUCTION OF THE UPPER LIMBS/
Authors: CONCOLINO D SPERLI D CINTI R STRISCIUGLIO P ANDRIA G
Citation: D. Concolino et al., A MILD FORM OF ROBERTS SC PHOCOMELIA SYNDROME WITH ASYMMETRICAL REDUCTION OF THE UPPER LIMBS/, Clinical genetics, 49(5), 1996, pp. 274-276
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
PARTIAL TRISOMY-1 (Q42-]QTER) - A NEW CASE WITH A MILD PHENOTYPE
Authors: CONCOLINO D CINTI R FERRARO L MORICCA MT STRISCIUGLIO P
Citation: D. Concolino et al., PARTIAL TRISOMY-1 (Q42-]QTER) - A NEW CASE WITH A MILD PHENOTYPE, American journal of human genetics, 57(4), 1995, pp. 614-614
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
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