VARIABILITY OF R(22) CHROMOSOME PHENOTYPICAL EXPRESSION.DALLAPICCOLA B; BRINCHI V; CURATOLO P et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 3-4; PP. 287-290; BIBL. 4 REF.Article

INFANTILE SPASMS AND THE CHARGE ASSOCIATIONCURATOLO P; LIBUTTI G; BRINCHI V et al.1983; DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY; ISSN 0012-1622; GBR; DA. 1983; VOL. 25; NO 3; PP. 367-369; ABS. FRE/GER/SPA; BIBL. 6 REF.Article

ABSENCE OF CHROMOSOME HETEROGENEITY BETWEEN CLASSICAL FANCONI'S ANEMIA AND THE ESTREN-DAMESHEK TYPEDALLAPICCOLA B; ALIMENA G; BRINCHI V et al.1980; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1980; VOL. 2; NO 4; PP. 349-360; BIBL. 20 REF.Article

LA SINDROME R(22). = LE SYNDROME R(22)CURATOLO P; PAOLELLA A; PORRO G et al.1978; CLIN. PEDIATR.; ITAL.; DA. 1978; VOL. 60; NO 1; PP. 10-17; ABS. ANGL.; BIBL. 11 REF.Article

IDENTIFICATION OF THE ORIGIN OF A 22P+ CHROMOSOME BY TRIPLEX DOSAGE EFFECT OF LDH B, GAPHD, TPI AND ENO2DALLAPICCOLA B; BRINCHI V; MAGNANI M et al.1980; ANN. GENET.; FRA; DA. 1980; VOL. 23; NO 2; PP. 111-113; ABS. FRE; BIBL. 10 REF.Article

DUE CASI DI SINDROME 18P-ED UN CASO DI TRISOMIA 18P IN UNA STESSA FRATRIA. = DEUX CAS DE SYNDROME 18P- ET UN CAS DE TRISOMIE 18P DANS UNE MEME FRATRIEROSANO M; DE SALAZAR E; BRINCHI V et al.1977; NEUROPSICHIATR. INFANT.; ITAL.; DA. 1977; NO 197; PP. 1221-1237; ABS. ANGL.; BIBL. 3 P. 1/2Article

T(21Q21Q)/R(T(21Q21P)) MOSAIC IN TWO UNRELATED PATIENTS WITH MILD STIGMATA OF DOWN'S SYNDROMEDALLAPICCOLA B; BIANCO I; BRINCHI V et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 1; PP. 56-58; ABS. ENG; BIBL. 4 REF.Article

Increased chromosomal breakage in epileptic children after long-term treatmentCURATOLO, P; BRINCHI, V; CUSMAI, R et al.European journal of pediatrics. 1986, Vol 145, Num 5, pp 439-442, issn 0340-6199Article

Ultrastructural and biological characterization of human choroid cell cultures transformed by simian virus 40CARRUBA, G; DALLAPICCOLA, B; BRINCHI, V et al.In vitro. 1983, Vol 19, Num 6, pp 443-452, issn 0073-5655Article

Mating between two balanced translocation carriers in two unrelated familiesDALLAPICCOLA, B; CHESSA, L; BRINCHI, V et al.Human genetics. 1983, Vol 65, Num 2, pp 165-168, issn 0340-6717Article

Analyse chromosomique de 200 couples affectés par des avortements à répétition = Chromosomal analysis of 200 couples affected by repeatea spontaneous abortionsVIGNETTI, P; CASTELLI GATTINARA, G; BARLETTA, C et al.Bordeaux médical. 1987, Vol 20, Num 3-4, pp 29-33, issn 0021-7867Article