Citation: S. Manoukian et al., MALIGNANT-MELANOMA AND CHARCOT-MARIE-TOOTH DISEASE - A FURTHER CASE, American journal of medical genetics, 68(2), 1997, pp. 242-242
Authors:
RIVA P
CASTORINA P
MANOUKIAN S
DALPRA L
DONEDA L
MARINI G
DENDUNNEN J
LARIZZA L
Citation: P. Riva et al., CHARACTERIZATION OF A CYTOGENETIC 17Q11.2 DELETION IN AN NF1 PATIENT WITH A CONTIGUOUS GENE SYNDROME, Human genetics, 98(6), 1996, pp. 646-650
Authors:
BRISCIOLI V
MANOUKIAN S
SELICORNI A
LIVINI E
LALATTA F
Citation: V. Briscioli et al., KAUFFMAN OCULOCEREBROFACIAL SYNDROME IN A GIRL OF 15 YEARS, American journal of medical genetics, 58(1), 1995, pp. 21-23
Authors:
LARIZZA L
RIVA P
CASTORINA P
DALPRA L
DONEDA L
MANOUKIAN S
Citation: L. Larizza et al., CYTOGENETIC AND MOLECULAR STUDIES ON NF1 PATIENTS WITH DYSMORPHISM AND MENTAL-RETARDATION, American journal of human genetics, 57(4), 1995, pp. 521-521
Authors:
TURCO AE
PEISSEL B
ROSSETTI S
SELICORNI A
MANOUKIAN S
BRUSASCO A
TADINI G
GALIMBERTI A
TASSIS B
TUROLLA L
TENCONI R
PIGNATTI PF
Citation: Ae. Turco et al., PRENATAL TESTING IN A FETUS AT RISK FOR AUTOSOMAL-DOMINANT POLYCYSTICKIDNEY-DISEASE AND AUTOSOMAL RECESSIVE JUNCTIONAL EPIDERMOLYSIS-BULLOSA WITH PYLORIC ATRESIA, American journal of medical genetics, 47(8), 1993, pp. 1225-1230