REGIONAL MAPPING OF THE LOCUS FOR HEXOKINASE-1 (HK1)MAGNANI M; DALLAPICCOLA B.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 2; PP. 181; BIBL. 5 REF.Article

METODICHE DI BANDEGGIAMENTO CROMOSOMICO. = METHODES D'INDUCTION DE BANDES CHROMOSOMIQUESFORABOSCO A; DALLAPICCOLA B.1975; FOLIA HERED. PATHOL.; ITAL.; DA. 1975; VOL. 24; NO 4; PP. 66-89; ABS. ANGL.; BIBL. 3 P. 1/2Serial Issue

LE NUOVE SINDROMI AUTOSOMICHE = LES NOUVEAUX SYNDROMES AUTOSOMIQUESDALLAPICCOLA B; FORABOSCO A.1975; FOLIA HERED. PATHOL.; ITAL.; DA. 1975; VOL. 24; NO 3; PP. 32-67; ABS. ANGL.; BIBL. 5 P. 1/2Article

MALFORMAZIONI SCHELETRICHE DA ABERRAZIONI CROMOSOMICHE = LES MALFORMATIONS SQUELETTIQUES DANS LES ABERRATIONS CHROMOSOMIQUESDALLAPICCOLA B; PISTOCCHI GF.1972; MINERVA MED.; ITAL.; DA. 1972; VOL. 63; NO 92; PP. 5049-5268; ABS. ANGL.; BIBL. 15REF.Serial Issue

INACTIVE NORMAL X IN A FEMALE LEUKAEMIC PATIENT WITH AN ACQUIRED X/AUTOSOME TRANSLOCATIONDALLAPICCOLA B; ALIMENA G.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 2; PP. 169-177; BIBL. 20 REF.Article

L'ARILSOLFATASI A: UTILITA E LIMITI NELLA DIAGNOSI DIFFERENZIALE DELLE LEUCEMIE = LES ARYLSULFATASES A: UTILITE ET LIMITES DANS LE DIAGNOSTIC DIFFERENTIEL DES LEUCEMIESDALLAPICCOLA B; CARANDINA G.1972; HAEMATOLOGICA; ITAL.; DA. 1972; VOL. 57; NO 1-2; PP. 25-42; ABS. ANGL.; BIBL. 1P.1/2Serial Issue

OBSERVATIONS ON SPECIFIC GIEMSA STAINING OF THE Y AND ON SELECTIVE OIL DESTAINING OF THE CHROMOSOMES = OBSERVATIONS SUR LA COLORATION SPECIFIQUE DE L'Y PAR LE GIEMSA ET SUR LA DECOLORATION SELECTIVE DES CHROMOSOMES PAR L'HUILEDALLAPICCOLA B; RICCI N.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 26; NO 3; PP. 251-255; BIBL. 5REF.Article

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

DE NOVO TRISOMY 1611->PTERDALLAPICCOLA B; CURATOLO P; BALESTRAZZI P et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 49; NO 1; PP. 1-6; BIBL. 6 REF.Article

NEW AUTOSOMAL SYNDROMES: TRISOMIES 4 P AND 9 P.DALLAPICCOLA B; MASTROIACOVO P; SEGNI G et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 3-4; PP. 267-273; ABS. ITAL. FR. ALLEM.; BIBL. 9 REF.Article

THE RADIOLOGICAL PATTERN ASSOCIATED WITH THE TRISOMY OF THE SHORT ARM OF CHROMOSOME NO4 = LE TABLEAU RADIOLOGIQUE ASSOCIE A LA TRISOMIE DU BRAS COURT DU CHROMOSOME N^O4DALLAPICCOLA B; GIOVANNELLI G; FORABOSCO A et al.1975; PEDIATR. RADIOL.; GERM.; DA. 1975; VOL. 3; NO 1; PP. 34-40; BIBL. 23REF.Article

DERMATOGLYPHIC AND SKELETAL HAND ABNORMALITIES IN TURNER'S SYNDROME. A TENTATIVE SCORING METHOD = ANOMALIES DERMATOGLYPHIQUES ET SQUELETTIQUES DES MAINS DANS LE SYNDROME DE TURNER. UNE METHODE PROVISOIRE DE NOTATIONDALLAPICCOLA B; BAGNI B; PISTOCCHI G et al.1972; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1972; VOL. 21; NO 1-2; PP. 69-78; ABS. ITAL. FR. ALLEM.; BIBL. 11 REF.Article

A COMMENT ON THE PAPER: RECURRENCE OF DOWN SYNDROME ASSOCIATED WITH MICROCHROMOSOME BY C. RAMOS, L. RIVERA, J. BENITEZ, E. TEJEDOR, AND A. SANCHEZ-CASCOSCALABRO A; LUNGAROTTI MS; DALLAPICCOLA B et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 53; NO 2; PP. 287-288; BIBL. 6 REF.Article

AICARDI SYNDROME IN A MALE INFANTCURATOLO P; LIBUTTI G; DALLAPICCOLA B et al.1980; J. PEDIATR.; USA; DA. 1980; VOL. 96; NO 2; PP. 286-287; BIBL. 5 REF.Article

TRISOMY 2Q.DALLAPICCOLA B; FORABOSCO A; CALABRO A et al.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 3-4; PP. 307-310; BIBL. 9 REF.Article

Otofaciocervical syndrome : a sporadic patient supports splitting from the branchio-oto-renal syndromeDALLAPICCOLA, B; MINGARELLI, R.Journal of medical genetics. 1995, Vol 32, Num 10, pp 816-818, issn 0022-2593Article

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

PARTIAL TRISOMY 8Q RESULTING FROM MATERNAL TRANSLOCATION T(2;8)(Q373;Q23)GIORGI PL; TARANTINO E; FORMICA A et al.1978; ACTA GENET. MED. GEMELLOL.; ITA; DA. 1978; VOL. 27; PP. 75-79; BIBL. 6 REF.Article

CYTOGENETIC STUDIES IN ACUTE LEUKAEMIAS. PROGNOSTIC IMPLICATIONS OF CHROMOSOME IMBALANCES.ALIMENA G; ANNINO L; BALESTRAZZI P et al.1977; ACTA HAEMATOL.; SUISSE; DA. 1977; VOL. 58; NO 4; PP. 234-239; BIBL. 1 P. 1/2Article

TRISOMY 4P: FIVE NEW OBSERVATIONS AND OVERVIEW.DALLAPICCOLA B; MASTROIACOVO PP; MONTALI E et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 12; NO 6; PP. 344-356; BIBL. 1 P.Article

DE NOVO DUPLICATION 1Q32-Q42: VARIABILITY OF PHENOTYPIC FEATURES IN PARTIAL 1Q TRISOMICSLUNGAROTTI MS; FALORNI A; CALABRO A et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 5; PP. 398-402; BIBL. 27 REF.Article

CONFIRMATION OF REGIONAL ASSIGNMENT OF NUCLEOSIDE PHOSPHORYLASE TO BAND 14Q13 BY GENE-DOSAGE STUDIESDALLAPICCOLA B; MAGNANI M; DACHA M et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 341-343; BIBL. 6 REF.Article

COMPLEX TRANSLOCATION T(9;21) (9;22) (Q12P13) (Q12Q11) IN THE FAMILY OF A CHILD WITH 9P TRISOMY SYNDROME.DALLAPICCOLA B; BOLLEA G; MAZZILLI C et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 1; PP. 73-76; BIBL. 6 REF.Article

LEUCOCYTE MORPHOLOGY AND CHROMOSOME MORPHOLOGY = MORPHOLOGIE LEUCOCYTAIRE ET MORPHOLOGIE CHROMOSOMIQUEDALLAPICCOLA B; BARICORDI O; CAPRA L et al.1975; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1975; VOL. 24; NO 1-2; PP. 83-95; ABS. ITAL. FR. ALLEM.; BIBL. 1 P. 1/2Article

Reply to letter by M. Poot and H. HoehnPORFIRIO, B; DALLAPICCOLA, B.Human genetics. 1990, Vol 84, Num 6, pp 582-583, issn 0340-6717, 2 p.Article