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TWO B/C TRANSLOCATIONS SPECIFICALLY IDENTIFIED BY BANDING TECHNIQUES AS 46, XY, T (5 P + 6 Q-) AND 46, XX, T (4Q - 7 P +) = DEUX TRANSLOCATIONS B/C IDENTIFIEES DE FACON SPECIFIQUE PAR ETUDE DES BANDES CHROMOSOMIQUES: 46, XY, T (5 P + 6 Q-) ET 46, XX, T (4Q- 7 P +)COHEN MM; LIN CC; DAVIDSON RG et al.1972; J. MED. EXPER. CLIN.; SWITZ.; DA. 1972; VOL. 3; NO 4-5; PP. 216-223; BIBL. 6 REF.Serial Issue

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

A (5; 14) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-589.BORGAONKAR DS; ARONSON MM; GREENE AE et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 4; PP. 242Article

CRI-DU-CHAT SYNDROME COMBINED WITH PARTIAL C-GROUP TRISOMY = SYNDROME DU CRI-DU-CHAT ASSOCIE A UNE TRISOMIE PARTIELLE DANS LE GROUPE CMANN J; RAFFERTY JH.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 3; PP. 289-292; BIBL. 5 REF.Serial Issue

A CRI-DU-CHAT INFANT BORN TO A MOTHER CARRYING A 5/17 BALANCED TRANSLOCATION.KADOTANI T; HIYAMA Y; KAWAKAMI M et al.1977; PROC. JAP. ACAD.; JAP.; DA. 1977; VOL. 53; NO 3; PP. 155-158; BIBL. 10 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

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

"CRI DU CHAT" SYNDROME DUE TO A COMPLEX REARRANGEMENT OF CHROMOSOME 5FRANCESCONI D; ZUFFARDI O; D'ATTOMA G et al.1978; ANN. GENET.; FRA; DA. 1978; VOL. 21; NO 2; PP. 113-115; ABS. FRE; BIBL. 8 REF.Article

PARTIAL DISTAL TRISOMY 13Q RESULTING FROM FAMILIAL RECIPROCAL 5/13 TRANSLOCATIONYANAGISAWA S; YOKOYAMA H; AGENA N et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 45; NO 3; PP. 345-350; BIBL. 14 REF.Article

TRISOMIE PARTIELLE POUR LA PARTIE DISTALE DU BRAS COURT D'UN CHROMOSOME 11 PAR TRANSLOCATION 11/5 PATERNELLEBAJOLLE F; RULLIER J; PICARD AM et al.1978; ANN. GENET.; FRA; DA. 1978; VOL. 21; NO 3; PP. 181-185; ABS. ENG; BIBL. 9 REF.Article

"COMPLETE 5P" TRISOMY: 1 CASE AND 19 TRANSLOCATION CARRIERS IN 6 GENERATIONS.BRIMBLECOMBE FSW; LEWIS FJ; VOWLES M et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 4; PP. 271-275; BIBL. 9 REF.Article

MEIOTIC BEHAVIOR OF FIVE HUMAN RECIPROCAL TRANSLOCATIONS.CHANDLEY AC; SEUANEZ H; FLETCHER JM et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 2; PP. 98-111; BIBL. 20 REF.Article

PARTIAL MONOSOMY OF THE LONG ARM OF CHROMOSOME 16: A DISTINCT CLINICAL ENTITY.FRYNS JP; BANDE KNOPS J; VAN DEN BERGHE H et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 46; NO 1; PP. 115-120; BIBL. 9 REF.Article

HUMAN MEIOSIS. III: ELECTRON MICROSCOPICAL ANALYSIS OF CHROMOSOME PAIRING IN AN INDIVIDUAL WITH A BALANCED TRANSLOCATION 46,XY,T (5P-;22P+)HOLM PB; RASMUSSEN SW.1978; CARLSBERG RES. COMMUNIC.; DNK; DA. 1978; VOL. 43; NO 5; PP. 329-350; BIBL. 33 REF.Article

INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 7 46, XX, DEL (7) (PTER->Q2200:Q3200->QTER)FRANCESCHINI P; SILENGO MC; DAVI GF et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 44; NO 3; PP. 345-348; BIBL. 7 REF.Article

PARTIAL DUPLICATION 5Q SYNDROME: PHENOTYPIC SIMILARITY IN TWO SISTERS WITH IDENTICAL KARYOTYPE (PARTIAL DUPLICATION 5Q33->5QTER AND PARTIAL DEFICIENCY (8P23->PTER).BARTSCH SANDHOFF M; LIERSCH R.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 4; PP. 281-284; ABS. FR.; BIBL. 5 REF.Article

CRI-DU-CHAT SYNDROME IN A CHILD WITH A 5/15 TRANSLOCATION AND INTERSTITIAL CENTROMETRIC HETEROCHROMATINGEBAUER HJ; STUMPF B; HANSMANN I et al.1978; CLIN. GENET.; DNK; DA. 1978; VOL. 14; NO 6; PP. 345-350; BIBL. 30 REF.Article

ETUDE CYTOGENETIQUE D'UN NOUVEAU CAS DE TRISOMIE 12P.ANDRE MJ.1976; BULL. ASS. ANATOMISTES; FR.; DA. 1976; VOL. 60; NO 170; PP. 455-463; ABS. ANGL.; BIBL. 5 REF.Article

PARTIAL TRISOMY FOR THE DISTAL LONG ARM OF CHROMOSOME 5 (REGION Q34->QTER). A NEW CLINICALLY RECOGNIZABLE SYNDROMECURRY CJR; LOUGHMAN WD; FRANCKE U et al.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 5; PP. 454-461; BIBL. 4 REF.Article

A TDIC (5; 15) (P13; P11) CHROMOSOME SHOWING VARIATION FOR CONSTRICTION IN THE CENTROMERIC REGIONS IN A PATIENT WITH THE CRI DU CHAT SYNDROMEDEWALD GW; BOROS SJ; CONROY MM et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 24; NO 1; PP. 15-26; BIBL. 22 REF.Article

NEW CHROMOSOMAL DYSMORPHIC SYNDROME. II. TRISOMY 10P.STENGEL RUTKOWSKI S; MURKEN JD; FRENKENBERGER R et al.1977; EUROP. J. PEDIATR.; GERM.; DA. 1977; VOL. 126; NO 3; PP. 109-125; ABS. ALLEM.; BIBL. 21 REF.Article

TWO RECIPROCAL TRANSLOCATIONS ASSOCIATED WITH MICROCEPHALY AND RETARDATION.BELL EF; WARBURTON D.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 2; PP. 141-142; BIBL. 1 REF.Article

MENTAL RETARDATION WITH 45 CHROMOSOMES 45, XX,-5,-14, + DER (5) T(5,14)(P15; Q13) MAT DUE TO FAMILIAL BALANCED RECIPROCAL TRANSLOCATION.FRIED K; TIEDER M; BEER S et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 1; PP. 68-72; BIBL. 7 REF.Article

PARTIAL MONOSOMY 22 AS THERESULT OF AN UNBALANCED TRANSLOCATION 5: 22 IN A PATIENT WITH CRI-DU CHAT-SYNDROME.SILENGO MC; ANDRIA G.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 34; NO 3; PP. 319-322; BIBL. 4 REF.Article

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