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PRENATAL DIAGNOSIS OF AN INHERITED TRANSLOCATION BETWEEN CHROMOSOMES NOS 9 ET 18EBBIN AJ; WILSON MG; TOWNER JW et al.1973; J. MED. GENET.; G.B.; DA. 1973; VOL. 10; NO 1; PP. 65-69; BIBL. 5REF.Serial Issue

TWO HUMAN X-AUTOSOME TRANSLOCATIONS IDENTIFIED BY AUTORADIOGRAPHY AND FLUORESCENCE = DEUX TRANSLOCATIONS AUTOSOME-X HUMAINES IDENTIFIEES PAR AUTORADIOGRAPHIE ET FLUORESCENCECOHEN MM; CHYI CHYANG LIN; SYBER V et al.1972; AMER. J. HUM. GENET.; U.S.A.; DA. 1972; VOL. 24; NO 5; PP. 583-597; BIBL. 2 P.Serial Issue

A CASE OF PARTIAL 14 TRISOMY 47,XY, (14Q-)+ AND TRANSLOCATION T (9P+; 14Q-) IN MOTHER AND BROTHER = UN CAS DE TRISOMIE 14 PARTIELLE 47, XY, (14Q-)+ AVEC TRANSLOCATION T (9P+; 14Q-) CHEZ LA MERE ET LE FRERESHORT EM; SOLITAIRE GB; BREG WR et al.1972; J. MED. GENET.; G.B.; DA. 1972; VOL. 9; NO 3; PP. 367-373; BIBL. 16 REF.Serial Issue

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

TRIPLE MOSAICISM WITH TWO AUTOSOMALLY UNBALANCED CELL LINES IN A PHENOTYPICALLY NORMAL OLIGOSPERMIC MAN.SHABTAI F; BICHACHO S; HALBRECHT I et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 2; PP. 177-180; BIBL. 15 REF.Article

HUMAN X-AUTOSOME TRANSLOCATIONS: DIFFERENTIAL INACTIVATION OF THE X CHROMOSOME IN A KINDRED WITH AN X-9 TRANSLOCATION = TRANSLOCATIONS HUMAINES X-AUTOSOME: INACTIVATION DIFFERENTIELLE DU CHROMOSOME X DANS UNE FAMILLE AYANT UNE TRANSLOCATION X-9LEISTI JT; KABACK MM; RIMOIN DL et al.1975; AMER. J. HUM. GENET.; U.S.A.; DA. 1975; VOL. 27; NO 4; PP. 441-453; BIBL. 1 P. 1/2Article

A (9; 17) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. 6M-988.LIN CC; KAVANAGH AJ; ARONSON MM et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 4; PP. 244Article

PARTIAL 9Q TRISOMY ASSOCIATED WITH A 9,21 TRANSLOCATION.CHAMLA Y; BILBEISSI C; MICHEAU M et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 38; NO 2; PP. 245-248; BIBL. 7 REF.Article

LA TRISOMIE 9P. UN CAS DE TRANSLOCATION T(9;22) (P11;P11)-MAT CHEZ UNE FILLETTE.GENEST P; ROUSSY J; GENEST FB et al.1977; UN. MED. CANADA; CANADA; DA. 1977; VOL. 106; NO 7; PP. 956-959; ABS. ANGL.; BIBL. 14 REF.Article

A NEX TRANSLOCATION INVOLVING THREE CHROMOSOMES IN CHRONIC MYELOCYTIC LEUKEMIA, 46, XY, T(9;11;22).GAHRTON G; FRIBERG K; ZECH L et al.1977; CYTOGENET. CELL GENET.; SWITZ; DA. 1977; VOL. 18; NO 2; PP. 75-81; BIBL. 1 P. 1/2Article

9P TRISOMY: A NEW CASE DUE TO MATERNAL T(9;18) TRANSLOCATION.PRETO A; LENZINI E; DRIGO P et al.1977; ACTA GENET. MED. GEMELLOL.; ITAL.; DA. 1977; VOL. 26; NO 3-4; PP. 283-286; BIBL. 1 P. 1/2Article

A PERICENTRIC INVERSION OF CHROMOSOME 9 AND A REARRANGEMENT INVOLVING CHROMOSOMES 9 AND 10 OBSERVED IN TWO GENERATIONS. CLINICAL DESCRIPTION OF CHROMOSOME 9 (P12-P21) DELATION SYNDROMEFALLSTROM SP; WAHLSTROM J.1979; CLIN. GENET.; DNK; DA. 1979; VOL. 15; NO 6; PP. 480-486; BIBL. 14 REF.Article

INTERCHROMOSOMAL DUPLICATION FOR THE SHORT ARM OF CHROMOSOME NO. 9: REPORT OF THREE CASES DUE TO A FAMILIAL TRANSLOCATION T(9; 11) AND ONE CASE WITH A DE NOVO 47, XX, +9P KARYOTYPE.LIN CC; HOLMAN G; SEWELL L et al.1977; J. MENTAL DEFIC. RES.; G.B.; DA. 1977; VOL. 21; NO 4; PP. 309-320; BIBL. 1 P. 1/2Article

FAMILIAL PARTIAL 14 TRISOMYMILLER JQ; WILLSON K; WYANDT H et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 1; PP. 60-65; BIBL. 2 P.Article

,XX,+DER(18),T(9;18)(P24;Q21) MAT: A DISTINCT PARTIAL TRISOMY 18Q- SYNDROME.BASS HN; WEBER PARISI F; SPARKES RS et al.1978; J. MED. GENET.; GBR; DA. 1978; VOL. 15; NO 5; PP. 391-395; BIBL. 9 REF.Article

MEIOSIS IN TWO HUMAN RECIPROCAL TRANSLOCATIONSSAN ROMAN C; SORDO MT; GARCIA SAGREDO JM et al.1979; J. MED. GENET.; GBR; DA. 1979; VOL. 16; NO 1; PP. 56-59; BIBL. 10 REF.Article

LOCALISATION OF THE HUMAN ABO: NP-1:AK-1 LINKAGE GROUP BY REGIONAL ASSIGNMENT OF AK-1 TO 9Q34.FERGUSON SMITH MA; AITKEN DA; TURLEAU C et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 34; NO 1; PP. 35-43; BIBL. 1 P. 1/2Article

RESULTS OF DERMATOGLYPHIC ANALYSIS.LOESCH D.1977; J. MENTAL DEFIC. RES.; G.B.; DA. 1977; VOL. 21; NO 4; PP. 321-329; BIBL. 2 REF.Article

CONSTITUTIONAL CHROMOSOMAL ABERRATION, T(4;12) (Q23;P11), IN A PATIENT WITH PH1 POSITIVE CHRONIC MYELOCYTIC LEUKEMIAGAHRTON G; FRIBERG K; ZECH L et al.1978; HEREDITAS; SWE; DA. 1978; VOL. 89; NO 2; PP. 169-173; BIBL. 19 REF.Article

THE 9P-DELETION SYNDROME. A PATIENT WITH A 45, XX, -9, -15, + T(9/15) CONSTITUTION DUE TO MATERNAL 3:1 MEIOTIC DISJUNCTION.BERGAMO F; CROSATO F; FRANCESCONI D et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 3; PP. 219-223; BIBL. 10 REF.Article

A NEW COMPLEX PH1 TRANSLOCATION INVOLVING THREE CHROMOSOMES: BRIEF COMMUNICATION.SONTA SI; SANDBERG AA.1977; J. NATION. CANCER INST.; U.S.A.; DA. 1977; VOL. 58; NO 6; PP. 1583-1586; BIBL. 18 REF.Article

CYTOGENETIC DISORDERS.1976; BIRTH DEFECTS ORIGIN. ATRICLE SER.; U.S.A.; DA. 1976; VOL. 12; NO 5; PP. 87-177; BIBL. DISSEM.; (CYTOGENET. ENVIRON. MALFORM. SYNDROMES. CONF.; KANSAS CITY, MO.; 1975)Article

SINGLE CD BAND IN DICENTRIC TRANSLOCATIONS WITH ONE SUPPRESSED CENTROMEREDANIEL A.1979; HUM. GENET.; DEU; DA. 1979; VOL. 48; NO 1; PP. 85-92; BIBL. 2 P.Article

ISOCHROMOSOME 17 Q IN TWO CASES OF ACUTE BLAST TRANSFORMATION IN MYELOPROLIFERATIVE DISORDERSMCDERMOTT A; ROMAIN D; FRASER ID et al.1978; HUM. GENET.; DEU; DA. 1978; VOL. 45; NO 2; PP. 215-218; BIBL. 4 REF.Article

P TRISOMY: A SYNDROME.JOE JIE HOO.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 4; PP. 261-263; ABS. FR.; BIBL. 7 REF.Article

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