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Results:
1-13
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Results: 13
Authors:
BRUGNONI R
MORANDI L
BRAMBATI B
BRISCIOLI V
CORNELIO F
MANTEGAZZA R
Citation: R. Brugnoni et al., A NEW NONRADIOACTIVE METHOD FOR THE SCREENING AND PRENATAL-DIAGNOSIS OF MYOTONIC-DYSTROPHY PATIENTS, Journal of neurology, 245(5), 1998, pp. 289-293
Authors:
RUSSO S
BRISCIOLI V
COGLIATI F
MACCHI M
LALATTA F
LARIZZA L
Citation: S. Russo et al., AN UNUSUAL FRAGILE-X SIBSHIP - FEMALE COMPOUND HETEROZYGOTE AND MALE WITH A PARTIALLY METHYLATED FULL MUTATION, Clinical genetics, 54(4), 1998, pp. 309-314
Authors:
PARINI O
BRISCIOLI V
CARUSO U
DORCHE C
FORTUNA R
MINNITI G
SELICORNI A
VISMARA E
MANCINI G
Citation: O. Parini et al., SPHEROPHAKIA ASSOCIATED WITH MOLYBDENUM COFACTOR DEFICIENCY, American journal of medical genetics, 73(3), 1997, pp. 272-275
Authors:
BRISCIOLI V
LALATTA F
RIZZUTI T
FESSLOVA V
Citation: V. Briscioli et al., THOMAS SYNDROME - CLINICAL VARIABILITY AND AUTOSOMAL RECESSIVE INHERITANCE, American journal of medical genetics, 71(3), 1997, pp. 373-374
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:
MAROTEAUX P
BRISCIOLI V
LALATTA F
BONAVENTURE J
Citation: P. Maroteaux et al., ODONTOCHONDRODYSPLASIA, Archives de pediatrie, 3(6), 1996, pp. 549-554
Authors:
VIANI F
ROMEO A
VIRI M
MASTRANGELO M
LALATTA F
SELICORNI A
GOBBI G
LANZI G
BETTIO D
BRISCIOLI V
DISEGNI M
PARINI R
TERZOLI G
Citation: F. Viani et al., SEIZURE AND EEG PATTERNS IN ANGELMANS SYNDROME, Journal of child neurology, 10(6), 1995, pp. 467-471
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:
BETTIO D
RIZZI N
GIARDINO D
GRUGNI G
BRISCIOLI V
SELICORNI A
CARNEVALE F
LARIZZA L
Citation: D. Bettio et al., FISH ANALYSIS IN PRADER-WILLI AND ANGELMAN SYNDROME PATIENTS, American journal of medical genetics, 56(2), 1995, pp. 224-228
Authors:
VIANI F
BEGHI E
LALATTA F
BESANA D
CERNIBORI A
GOBBI G
LANZI G
MONTRASIO V
PERENCHIO MT
TIBERTI A
BRISCIOLI V
CERATI D
CONTE S
GARAVELLI L
GIORDANO L
MARTINELLI O
MUZIO O
RASMINI P
ROSI C
ROMEO A
SELICORNI A
VEGGIOTTI P
VIRI M
MONTICELLI ML
Citation: F. Viani et al., SURVEY OF THE PREVALENCE, CLINICAL AND GENETIC-ASPECTS OF ANGELMAN SYNDROME IN 7 LOCAL HEALTH DISTRICTS OF ITALY, Epilepsia, 36, 1995, pp. 2-2
Authors:
GIARDINO D
RIZZI N
BRISCIOLI V
BETTIO D
Citation: D. Giardino et al., A DE-NOVO 6Q11-Q15 DUPLICATION INVESTIGATED BY CHROMOSOME PAINTING, Clinical genetics, 46(5), 1994, pp. 377-379
Authors:
SELICORNI A
LALATTA F
LIVINI E
BRISCIOLI V
PIGUZZI T
BAGOZZI DC
MASTROIACOVO P
ZAMPINO G
GAETA G
PUGLIESE A
CERUTTIMAINAROLI P
GUALA A
ZELANTE L
STABILE M
BELLI S
FRANCESCHINI P
GIANOTTI A
SCARANO G
Citation: A. Selicorni et al., VARIABILITY OF THE BRACHMANN-DELANGE SYNDROME, American journal of medical genetics, 47(7), 1993, pp. 977-982
Authors:
BRISCIOLI V
FLORIDIA G
ROSSI E
SELICORNI A
LALATTA F
ZUFFARDI O
Citation: V. Briscioli et al., TRISOMY 10QTER CONFIRMED BY IN-SITU HYBRIDIZATION, Journal of Medical Genetics, 30(7), 1993, pp. 601-603
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