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

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

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

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

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

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

DE NOVO APPEARANCE OF A TRANSLOCATION T(5P; 21Q), AND ITS TRANSMISSION IN BOTH BALANCED AND UNBALANCED FORMS TO THE NEXT GENERATIONCHAGANTI RSK; MORILLO CUCCI G; FRIIS L et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 1; PP. 43-48; ABS. FR.; BIBL. 23 REF.Article

DELETION-TRANSLOCATION DEL(12)(P11)->T(10;12)(P13;P11)NIELSEN J; RASMUSSEN K; NIEBUHR E et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 1; PP. 53-55; ABS. FR.; BIBL. 36 REF.Article

FAMILIAL TRANSLOCATION, T(2;5) (P 23; Q 31).OSZTOVICS M; KISS P.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 8; NO 2; PP. 112-116; BIBL. 2 REF.Article

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

ASPERMIA, ASSOCIATED WITH A PRESUMABLY BALANCED X/AUTOSOMAL TRANSLOCATION. KARYOTYPE 46,Y,T(X;5) (Q28;Q11)STENGEL RUTKOWSKI S; ZANKL H; RODEWALD A et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 31; NO 1; PP. 97-106; BIBL. 2 P. 1/2Article

EFFECT OF OUABAIN RESISTANCE ON HUMAN DIPLOID FIBROBLASTS CARRYING OTHER GENETIC VARIANTS = EFFET DE LA RESISTANCE A LA OUABAINE SUR DES FIBROBLASTES DIPLOIDES HUMAINS PORTANT D'AUTRES MARQUEURS GENETIQUESCORSARO CM; MIGEON BR.1975; EXPER. CELL RES.; U.S.A.; DA. 1975; VOL. 95; NO 1; PP. 47-53; BIBL. 12 REF.Article

PARTIAL TRISOMY FOR THE LONG ARMS OF CHROMOSOME NO 5 DUE TO INSERTION AND FURTHER "ANEUSOMIE DE RECOMBINAISON''JALBERT P; JALBERT H; SELE B et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 4; PP. 418-423; BIBL. 19 REF.Article