Authors:
DADAMO P
MENEGON A
LONIGRO C
GRASSO M
GULISANO M
TAMANINI F
BIENVENU T
GEDEON AK
OOSTRA B
WU SK
TANDON A
VALTORTA F
BALCH WE
CHELLY J
TONIOLO D
Citation: P. Dadamo et al., MUTATIONS IN GDI1 ARE RESPONSIBLE FOR X-LINKED NONSPECIFIC MENTAL-RETARDATION (VOL 19, PG 134, 1998), Nature genetics, 19(3), 1998, pp. 303-303
Authors:
DADAMO P
MENEGON A
LONIGRO C
GRASSO M
GULISANO M
TAMANINI F
BIENVENU T
GEDEON AK
OOSTRA B
WU SK
TANDON A
VALTORTA F
BALCH WE
CHELLY J
TONIOLO D
Citation: P. Dadamo et al., MUTATIONS IN GDI1 ARE RESPONSIBLE FOR X-LINKED NONSPECIFIC MENTAL-RETARDATION, Nature genetics, 19(2), 1998, pp. 134-139
Authors:
LONIGRO C
CHONG SS
SMITH ACM
DOBYNS WB
CARROZZO R
LEDBETTER DH
Citation: C. Lonigro et al., POINT MUTATIONS AND AN INTRAGENIC DELETION IN LIS1, THE LISSENCEPHALYCAUSATIVE GENE IN ISOLATED LISSENCEPHALY SEQUENCE AND MILLER-DIEKER SYNDROME, Human molecular genetics, 6(2), 1997, pp. 157-164
Authors:
MERONI G
REYMOND A
ALCALAY M
BORSANI G
TANIGAMI A
TONLORENZI R
LONIGRO C
MESSALI S
ZOLLO M
LEDBETTER DH
BRENT R
BALLABIO A
CARROZZO R
Citation: G. Meroni et al., ROX, A NOVEL BHLHZIP PROTEIN EXPRESSED IN QUIESCENT CELLS THAT HETERODIMERIZES WITH MAX, BINDS A NONCANONICAL E-BOX AND ACTS AS A TRANSCRIPTIONAL REPRESSOR (VOL 16, PG 2892, 1997), EMBO journal, 16(19), 1997, pp. 6055-6055
Authors:
MERONI G
REYMOND A
ALCALAY M
BORSANI G
TANIGAMI A
TONLORENZI R
LONIGRO C
MESSALI S
ZOLLO M
LEDBETTER DH
BRENT R
BALLABIO A
CARROZZO R
Citation: G. Meroni et al., ROX, A NOVEL BHLHZIP PROTEIN EXPRESSED IN QUIESCENT CELLS THAT HETERODIMERIZES WITH MAX, BINDS A NONCANONICAL E-BOX AND ACTS AS A TRANSCRIPTIONAL REPRESSOR, EMBO journal, 16(10), 1997, pp. 2892-2906
Authors:
FOGLI A
LONIGRO C
RENIERI A
FERNANDEZ E
PILZ D
LEDBETTER DH
GUERRINI R
CARROZZO R
Citation: A. Fogli et al., MUTATION ANALYSIS IN THE LIS1 GENE OF 14 PATIENTS WITH ISOLATED LISSENCEPHALY SEQUENCE, American journal of human genetics, 61(4), 1997, pp. 1950-1950
Authors:
PERRONI L
GRASSO M
ARGUSTI A
LONIGRO C
CROCI GF
ZELANTE L
GARANI GP
BRICARELLI FD
Citation: L. Perroni et al., MOLECULAR AND CYTOGENETIC ANALYSIS OF THE FRAGILE-X-SYNDROME IN A SERIES OF 453 MENTALLY-RETARDED SUBJECTS - A STUDY OF 87 FAMILIES, American journal of medical genetics, 64(1), 1996, pp. 176-180