Cytogenetic evidence of clonal evolution in a case of hemopoietic dysplasia with a 5q- chromosome = Mise en évidence cytogénétique de l'évolution clonale dans un cas de dysplasie hémopoïétique avec chromosome 5q9cTANIWAKI, M; EDAGAWA, J; SONODA, Y et al.Cancer genetics and cytogenetics. 1983, Vol 10, Num 1, pp 59-65, issn 0165-4608Article

SINDROMES 4P-Y 5P-(SU IDENTIFICACION POR EL ESTUDIO CROMOSOMICO). = SYNDROMES 4P- ET 5P. LEUR IDENTIFICATION PAR L'ETUDE CHROMOSOMIQUEPRIETO F; BADIA L; ORELLANA F et al.1975; REV. ESP. PEDIATR.; ESP.; DA. 1975; VOL. 31; NO 184; PP. 581-590; ABS. FR. ANGL. ALLEM.; BIBL. 1 P.Article

SINDROME DE MAULLIDO DE GATO. ESTUDIO COMPARATIVO EN EDADES DISTINTAS = SYNDROME DU CRI DU CHAT. ETUDE COMPARATIVE A DIVERS AGESANSEDE A; NOYA M; NOGUEIRA CAAMANO L et al.1974; MED. CLIN.; ESP.; DA. 1974; VOL. 63; NO 10; PP. 509-516; ABS. ANGL.; BIBL. 1P.1/2Article

Interstitial delection of band q12 of chromosome 5DUDIN, G; ALEXANDER, D; TALJ, F et al.Clinical genetics. 1984, Vol 25, Num 5, pp 455-458, issn 0009-9163Article

A PROPOS D'UNE OBSERVATION DE MALADIE DU CRI DU CHAT.CASTEL Y; TOUDIC L; RIVIERE D et al.1977; REV. INTERNATION. PEDIATR.; FR.; DA. 1977; NO 76; PP. 29-42; BIBL. 19 REF.Article

ETUDE MEIOTIQUE ET MITOTIQUE DANS UN CAS DE TRANSLOCATION T (5;Y).DUTRILLAUX B; GUEGUEN J.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 3; PP. 241-245; ABS. ANGL.; BIBL. 13 REF.Article

CYTOGENETIC RECOMBINANTS FROM A FEMALE CARRYING A PARACENTRIC INVERSION OF THE SHORT ARM OF CHROMOSOME NUMBER 5VALCARCEL E; BENITEZ J; MARTINEZ P et al.1983; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1983; VOL. 63; NO 1; PP. 78-81; BIBL. 12 REF.Article

DELETION OF THE SHORT ARM OF CHROMOSOME 5 FROM A SUBJECT WITH CRI-DU-CHAT SYNDROME. REPOSITORY IDENTIFICATION NO. GM71.BREG WR; ARONSON MM; GREENE AE et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 4; PP. 239-240; BIBL. 3 REF.Article

DEL (5P) WITHOUT "CRI DU CHAT" PHENOTYPEBACCICHETTI C.1982; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1982; VOL. 60; NO 4; PP. 389Article

CYTOGENETIQUE DU SYNDROME DU CRI DU CHATZHOU HUANGENG; KANG XUEZHEN; ZHANG QIANQIAN et al.1982; ACTA GENET. SIN.; CHN; DA. 1982; VOL. 9; NO 1; PP. 20-23; ABS. ENG; BIBL. 7 REF.Article

LE CONTRETYPE DE LA MALADIE DU CRI DU CHAT. LA TRISOMIE 5PSTOLL C; RETHORE MO; LAURENT C et al.1975; ARCH. FR. PEDIATR.; FR.; DA. 1975; VOL. 32; NO 6; PP. 551-561; ABS. ANGL.; BIBL. 13 REF.Article

REMANIEMENT COMPLEXE INTERESSANT LES CHROMOSOMES 3 ET 5 CHEZ UN ADOLESCENT MULTIMALFORMENAFFAH J; DER KALOUSTIAN V.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 121-124; ABS. ANGL.; BIBL. 6REF.Article

TRANSLOCATION 46,XY,T(2;5) (Q37; Q14) ET DEBILITE MENTALE. ETUDE CLINIQUE ET CYTOGENETIQUEGILGENKRANTZ S; WALBAUM R; MAUUARY G et al.1976; J. GENET. HUM.; SUISSE; DA. 1976; VOL. 24; NO 1; PP. 27-37; ABS. ANGL. ALLEM.; BIBL. 6 REF.Article

EVALUZIONE CLONALE IN UN CASO DI DELEZIONE = EVOLUTION CLONALE DANS UN CAS DE DELETIONZANOIO L; LAVEZZI AM.1973; FOLIA HERED. PATHOL.; ITAL.; DA. 1973; VOL. 22; NO 4; PP. 65-67; ABS. ANGL.; BIBL. 2REF.Article

Long arm deletion of chromosome 5 in a case of chronic myelomonocytic leukemiaSATO, Y; KUBOTA, K; SUDA, K et al.Cancer genetics and cytogenetics. 1985, Vol 15, Num 3-4, pp 269-275, issn 0165-4608Article

Acquired partial deletions of the long arm of chromosome 5 in hematologic disordersWISNIEWSKI, L. P; HIRSCHHORN, K.American journal of hematology. 1983, Vol 15, Num 3, pp 295-310, issn 0361-8609Article

Sindrome del grito del gato. Deleccion parcial del cromosoma 5 (fórmula: 46XY5p) = Syndrome du cri du chat. Délétion partielle du chromosome 5 (formule: 46XY5p) = Cat's cry. Partial deletion of chromosome 5: formula 46XY5pCARRAU, J; DELFINO, A; QUADRELLI, R et al.Archivos de Pediatria del Uruguay. 1983, Vol 53, Num 4, pp 234-238, issn 0004-0584Article

Inherited pericentric inversion of human chromosome 5BARBATA, G; GRANATA, G; CARBONE, P et al.Human genetics. 1983, Vol 65, Num 2, issn 0340-6717, 216Article

Franceschetti syndrome in a child with a de novo balanced translocation (5;13) (q11;p11) and significant decrease of hexosaminidase BBALESTRAZZI, P; BAETEMAN, M. A; MATTEI, M. G et al.Human genetics. 1983, Vol 64, Num 3, pp 305-308, issn 0340-6717Article

FETAL MANIFESTATION OF CHROMOSOMAL DISORDER: PARTIAL DUPLICATION OF THE LONG ARM OF CHROMOSOME 5 (5Q33->QTER)PASSARGE E; BARTSCH SANDHOFF M; REHDER H et al.1982; TERATOLOGY; ISSN 0040-3709; USA; DA. 1982; VOL. 25; NO 2; PP. 221-225; BIBL. 15 REF.Article

INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 5 IN A DEFORMED BOY: 46,XY,DEL(5) (Q13Q15)STOLL C; LEVY JM; ROTH MP et al.1980; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1980; VOL. 17; NO 6; PP. 486-487; BIBL. 4 REF.Article

DERMATOGLYPHICS IN CRI DU CHAT SYNDROME.SHIONO H; KADOWAKI JI; KAZAMA H et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 3; PP. 214-218; BIBL. 1 P.Article

PARTIAL TRISOMYL 5 WITH A CARRIER PARENT T(5P-;9P+)MONTELEON P; MONTELEON J; SEKHON G et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 4; PP. 437-440; BIBL. 9 REF.Article

CONSIDERAZIONI SU CINQUE CASI DI SINDROMI DI CRI DU CHAT. = DISCUSSIONS CONCERNANT CINQ CAS DE SYNDROME DU CRI DU CHATCERRUTI MAINARDI C; VIANELLO MG; BONIOLI E et al.1976; MINERVA PEDIATR.; ITAL.; DA. 1976; VOL. 28; NO 38; PP. 2389-2400; ABS. ANGL.; BIBL. 1 P.Article

BALANCED FAMILIAL TRANSLOCATION T(5;19) (Q12; P OR Q11) WITH PHENOTYPICAL ABNORMALITIES IN A GIRL. = TRANSLOCATION FAMILIALE BALANCEE T(5;19) (Q12; P OU Q11) AVEC ANOMALIES PHENOTYPIQUES CHEZ UNE FILLESTOLL C; LEVY JM; CHAMPY M et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 3; PP. 263-267; BIBL. 4 REF.Article