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Results: 5

Authors: MANOUKIAN S BRISCIOLI V LALATTA F
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
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