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

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

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

PARTIAL TRISOMIE 5Q: THREE DIFFERENT PHENOTYPES DEPENDING ON DIFFERENT DUPLICATION SEGMENTSRODEWALD A; ZANKL M; GLEY EO et al.1980; HUM. GENET.; DEU; DA. 1980; VOL. 55; NO 2; PP. 191-198; BIBL. 8 REF.Article

PRENATAL DIAGNOSIS OF 5 P.DAVID K; KAFFE S; STRAUSS L et al.1978; CLIN. GENET.; DENM.; DA. 1978; VOL. 13; NO 2; PP. 224-228; BIBL. 12 REF.Article

THE HETEROGENEITY OF THE 5Q-CHROMOSOME MARKER IN REFRACTORY ANEMIA = L'HETEROGENEITE DU MARQUEUR CHROMOSOMIQUE-5Q DANS L'ANEMIE REFRACTAIREWATT JL; KING DJ; PALMER JBD et al.1983; CANCER GENETICS AND CYTOGENETICS; ISSN 0165-4608; NLD; DA. 1983; VOL. 9; NO 2; PP. 113-118; ABS. ENG; BIBL. 13 REF.; FIGArticle

THE 5Q-CHROMOSOME ABNORMALITY IN HAEMATOLOGICAL DISORDERS: A COLLABORATIVE STUDY OF 34 CASES FROM THE NETHERLANDSKERKHOFS H; HAGEMEIJER A; LEEKSMA CHW et al.1982; BR. J. HAEMATOL.; ISSN 0007-1048; GBR; DA. 1982; VOL. 52; NO 3; PP. 365-381; BIBL. 2 P.Article

PARTIAL PROXIMAL TRISOMY OF THE LONG ARM OF CHROMOSOME 5(Q13->Q22) RESULTING FROM MATERNAL INSERTION DERMS (10;5)GILGENKRANTZ S; DULUCQ P; BRESSON J et al.1981; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1981; VOL. 18; NO 6; PP. 465-469; BIBL. 10 REF.Article

ANTHROPOMETRY IN THE CRI DU CHAT SYNDROMENIEBUHR E.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 16; NO 2; PP. 82-95; BIBL. 2 P.Article

CONSIDERAZIONI SU UN CASO DI SINDROME DEL CRI DU CHAT". = CONSIDERATIONS SUR UN CAS DE "SYNDROME DU CRI DU CHAT"DI PALMA L; IEMMA R; DI CESARE M et al.1978; MINERVA PEDIATR.; ITAL.; DA. 1978; VOL. 30; NO 2; PP. 173-177; ABS. ANGL.; BIBL. 34 REF.Article

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

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

THE 5Q-SYNDROME: AN UNDERDIAGNOSED FORM OF MACROCYTIC ANAEMIATINEGATE H; GAUNT L; HAMILTON PJ et al.1983; BRITISH JOURNAL OF HAEMATOLOGY; ISSN 0007-1048; GBR; DA. 1983; VOL. 54; NO 1; PP. 103-110; BIBL. 14 REF.Article

DUPLICATION (5P13->PTER): PRENATAL DIAGNOSIS AND REVIEW OF THE LITERATUREKHODR GS; CADENA G; LE KL et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 12; NO 1; PP. 43-49; BIBL. 13 REF.Article

INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME NO. 5 IN TWO UNRELATED CHILDREN WITH CONGENITAL ANOMALIES AND MENTAL RETARDATIONSILENGO MC; LUZZATTI L; CENTERWALL WR et al.1981; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1981; VOL. 19; NO 3; PP. 174-180; BIBL. 21 REF.Article

PURE RED CELL HYPOPLASIA ASSOCIATED WITH LONG-ARM DELETION OF CHROMOSOME 5DIBENEDETTO J JR; PADRE MENDOZA T; ALBALA MM et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 3; PP. 345-348; BIBL. 1 P.Article

SIMULTANEOUS OCCURRENCE OF 5Q- AND 21Q-IN REFRACTORY ANEMIA WITH THROMBOCYTOSISVAN DEN BERGHE H; PETIT P; BROECKAERT VAN ORSHOVEN A et al.1979; CANCER GENET. CYTOGENET.; USA; DA. 1979; VOL. 1; NO 1; PP. 63-68; BIBL. 7 REF.Article

PARTIAL TRISOMY FOR SHORT AND LONG ARM OF CHROMOSOME NO 5. TWO CASES OF TWO POSSIBLE SYNDROMES.ZABEL B; BAUMANN W; GEHLER J et al.1978; J. MED. GENET.; G.B.; DA. 1978; VOL. 15; NO 2; PP. 143-147; BIBL. 12 REF.Article

PARTIAL TRISOMY-5PYUNIS E; SILVA R; EGEL H et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 43; NO 2; PP. 231-237; BIBL. 7 REF.Article

TRISOMY 10P DUE TO T(5; 10) (P15;P11) SEGREGATING IN A LARGE SIBSHIP.BACK E; VOGEL W; HERTE C et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 1; PP. 11-17; BIBL. 18 REF.Article

LA MALADIE DU CRI DU CHAT. (A PROPOS DE QUATRE OBSERVATIONS PERSONNELLES).BOISSEAU C.1977; ; S.L.; DA. 1977; PP. 1-58; H.T. 2; BIBL. 13 P.; (THESE DOCT. MED.; TOURS)Thesis

LA SINDROME DEL "CRI DU CHAT". OSSERVAZIONI SU DUE NUOVI CASI IDENTIFICATI MEDIANTE BANDEGGIAMENTO R. = LE SYNDROME DU "CRI DU CHAT". OBSERVATIONS SUR DEUX NOUVEAUX CAS IDENTIFIES AU MOYEN DES BANDES RCAVAZZUTI GB; FORABOSCO A; TAMBORINO G et al.1976; CLIN. PEDIATR.; ITAL.; DA. 1976; VOL. 58; NO 12; PP. 585-603; ABS. ANGL.; BIBL. 6 REF.Article

DEFICIENCIA MENTAL E MALFORMACOES EM CRIANCA COM TRANSLOCACOES CROMOSSOMICAS 5/13. = DEFICIENCE MENTALE ET MALFORMATIONS CHEZ UN ENFANT AVEC DES TRANSLOCATIONS CHROMOSOMIQUES 5/13MOURA RIBEIRO V; FERRARI I; MOREIRA LMA et al.1976; ARQU. NEURO-PSIQUIATR.; BRAS.; DA. 1976; VOL. 34; NO 2; PP. 199-204; ABS. ANGL.; BIBL. 16 REF.Article