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Results 1 to 25 of 116681

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HABITUAL ABORTION AND TRANSLOCATION (22Q; 22Q): UNEXPECTED TRANSMISSION FROM A MOTHER TO HER PHENOTYPICALLY NORMAL DAUGHTERKIRKELS VGHJ; HUSTINX TWJ; SCHERES JMJC et al.1980; CLIN. GENET.; ISSN 0009-9163; DNK; DA. 1980; VOL. 18; NO 6; PP. 456-461; BIBL. 23 REF.Article

MEIOTIC SEGREGATION IN FAMILIAL RECIPROCAL TRANSLOCATION T (8Q; 22Q)GOEDDE SALZ E; OESINGHAUS S; GROTE W et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 11; NO 2; PP. 241-247; BIBL. 10 REF.Article

INCOMPLETE TRISOMY 22. II. FAMILIAL TRISOMY OF THE DISTAL SEGMENT OF CHROMOSOME 22Q IN TWO BROTHERS FROM A MOTHER WITH A TRANSLOCATION, T(6; 22) (Q27; Q13)SCHINZEL A.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 56; NO 3; PP. 263-268; BIBL. 5 REF.Article

THE 11Q; 22Q TRANSLOCATION: A EUROPEAN COLLABORATIVE ANALYSIS OF 43 CASESFRACCARO M; LINDSTEN J; FORD CE et al.1980; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1980; VOL. 56; NO 1; PP. 21-51; BIBL. 1 P.Article

PARTIAL TRISOMY OF 13 (PTER->Q12) DUE TO 47, XY,+DER (13), T(13; 22) (Q12; Q13)MATMOEDJONO SJ; SPARKES RS.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 241-246; BIBL. 19 REF.Article

TRANSLOCATION 21Q22Q IN AN INFERTILE HUMAN MALECHANDLEY AC; HARGREAVE TB; FLETCHER JM et al.1982; J. MED. GENET.; ISSN 0022-2593; GBR; DA. 1982; VOL. 19; NO 5; PP. 366-369; BIBL. 19 REF.Article

INCOMPLETE TRISOMY 22. I: FAMILIAL 11/22 TRANSLOCATION WITH 3:1 MEIOTIC DISJUNCTION. DELINEATION OF A COMMON CLINICAL PICTURE AND REPORT OF NINE NEW CASES FROM SIX FAMILIESSCHINZEL A; SCHMID W; DER MAUR PA et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 56; NO 3; PP. 249-262; BIBL. 2 P.Article

PARTIAL TRISOMY 13. THE MYTH OF NONMONGOLOID TRISOMY GPATIL SR; ZELLWEGER H.1981; CLIN. PEDIATR.; ISSN 0009-9228; USA; DA. 1981; VOL. 20; NO 8; PP. 534-536; BIBL. 15 REF.Article

CHRONIC MYELOGENOUS LEUKEMIA WITH TRANSLOCATIONS (3Q-; 9Q+) AND (17Q-; 22Q+). POSSIBLE CRUCIAL CYTOGENETIC EVENTS IN THE GENESES OF CMLOSHIMURA M; OHYASHIKI K; VEHARA M et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 1; PP. 48-51; BIBL. 21 REF.Article

9;22;15 COMPLEX TRANSLOCATION IN PH1 CHROMOSOME POSITIVE CML REVEALED BY GIEMSA-11 PROCEDURE IN APPARENT LYMPHOID CELLS OF BLASTIC CRISISHAYS T; MORSE HG; ROBINSON A et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 4; NO 4; PP. 283-292; BIBL. 16 REF.Article

A CASE OF TRISOMY 22 IN PONGO PYGMAEUSANDRLE M; FIEDLER W; RETT A et al.1979; CYTOGENET. CELL GENET.; CHE; DA. 1979; VOL. 24; NO 1; PP. 1-6; BIBL. 17 REF.Article

CHRONIC MYELOGENOUS LEUKEMIA WITH A COMPLEX TRANSLOCATIONMOHANDAS T; ANDERSON C; OKUN D et al.1980; CANCER GENET. CYTOGENET.; USA; DA. 1980; VOL. 2; NO 1; PP. 19-21; BIBL. 8 REF.Article

FAMILIAL Y-AUTOSOME TRANSLOCATION IN TWO UNRELATED GIRLSFUNDERBURK SJ; KLISAK I; SPARKES RS et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 2; PP. 119-122; ABS. FRE; BIBL. 24 REF.Article

RED BLOOD CELL GLUTATHIONE PROXIDASE IN SIMPLE TRISOMY 21 AND TRANSLOCATION 21/22KEDZIORA J; LUKASZEWICZ R; KOTER M et al.1982; EXPERIENTIA; ISSN 0014-4754; CHE; DA. 1982; VOL. 38; NO 5; PP. 543-544; BIBL. 20 REF.Article

TRANSLOCATIONS T (2;8) ET T (8;22) DANS DES LIGNEES CELLULAIRES CONTINUES DE LYMPHOMES DE BURKITT AFRICAINBERNHEIM A; BERGER R; LENOIR G et al.1980; C. R. HEBD. SEANCES ACAD. SCI., D; ISSN 0567-655X; FRA; DA. 1980; VOL. 291; NO 2; PP. 237-239; ABS. ENG; BIBL. 12 REF.Article

THE SIGNIFICANCE OF PH1 MOSAICISM: A REPORT OF SIX CASES OF CHRONIC GRANULOCYTIC LEUKAEMIA AND TWO CASES OF ACUTE MYELOID LEUKAEMIAWAYNE AW; SHARP JC; JOYNER MV et al.1979; BRIT. J. HAEMATOL.; GBR; DA. 1979; VOL. 43; NO 3; PP. 353-360; BIBL. 2 P.Article

KARYOTYPE EVOLUTION IN A CASE OF CHRONIC MYELOGENOUS LEUKEMIA WITH AN UNUSUAL PHILADELPHIA CHROMOSOME TRANSLOCATION, T(4;22), AND AN ADDITIONAL TRANSLOCATION, T(3;5)SESSAREGO M; BIANCHI SCARRA GL; AJMAR F et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 1; PP. 47-53; BIBL. 24 REF.Article

UNSTABLE FAMILIAL TRANSLOCATIONS: A T(11;22) MAT INHERITED AS A T(11;15)TOMKINS DJ.1981; AM. J. HUM. GENET.; ISSN 0002-9297; USA; DA. 1981; VOL. 33; NO 5; PP. 745-751; BIBL. 24 REF.Article

A BALANCED TRANSLOCATION (17,22) AND A PERICENTRIC INVERSION OF CHROMOSOME 5: REPOSITORY IDENTIFICATION NO. GM3196TESTA JR; ROWLEY JD; HAWKINS C et al.1980; CYTOGENET. CELL GENET.; CHE; DA. 1980; VOL. 27; NO 4; PP. 270Article

Approche moléculaire des remaniements du chromosome 22 humain observés dans des pathologies tumorales non hématologiques: cas particulier de la t(11; 22) du Sarcome = Molecular approach of human chromosome 22 rearrangements observed in non hematologic tumoral pathologies with particular interest to the t(11; 22) Ewing's sarcoma specific translocationDelattre, Olivier; Thomas, Gilles.1991, 117 p.Thesis

DOUBLE 9,22 TRANSLOCATION WITH HYPERDIPLOIDY APPEARING IN BLASTIC TRANSFORMATION OF CHRONIC GRANULOCYTIC LEUKEMIAPOORNIMA RAJASEKARIAH; ILLES I; GARSON OM et al.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 7; NO 1; PP. 85-88; BIBL. 5 REF.Article

SITE-SPECIFIC RECIPROCAL TRANSLOCATION, T(11;22) (Q23; Q11), IN SEVERAL UNRELATED FAMILIES WITH 3:1 MEIOTIC DISJUNCTIONZACKAI EH; EMANUEL BS.1980; AMER. J. MED. GENET.; USA; DA. 1980; VOL. 7; NO 4; PP. 507-521; BIBL. 50 REF.Article

PARTIAL TRISOMY OF 11 AND 22 DUE TO FAMILIAL TRANSLOCATION T(11;22)(Q23;Q11), INHERITED IN THREE GENERATIONSNAKAI H; YAMAMOTO Y; KUROKI Y et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 3; PP. 349-355; BIBL. 12 REF.Article

UN CAS DE TRISOMIE 22 INCOMPLETE DUE A LA MALSEGREGATION MEIOTIQUE D'UNE TRANSLOCATION FAMILIALE 11:22PESCIA G; JOTTERAND BELLOMO M; GAIDE AC et al.1981; REV. MED. SUISSE ROMANDE; ISSN 0035-3655; CHE; DA. 1981; VOL. 101; NO 4; PP. 325-329; BIBL. 6 REF.Article

TRISOMIE PARTIELLE 11Q PAR MALSEGREGATION D'UNE TRANSLOCATION MATERNELLE T(11; 22) (P23; P11.1)PANGALOS C; COUTURIER J; BARTSOCAS C et al.1980; NOUV. PRESSE MED.; ISSN 0301-1518; FRA; DA. 1980; VOL. 9; NO 41; PP. 3065-3067; ABS. ENG; BIBL. 7 REF.Article

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