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PARTIELLE FREIE TRISOMIE 13 IN EINER FAMILIE MIT BALANCIERTER TRANSLOKATION (13Q-; 16Q+) = UNE TRISOMIE 13 LIBRE PARTIELLE DANS UNE FAMILLE AVEC TRANSLOCATION BALANCEE (13Q-; 16Q+)SCHWANITZ G; GROSSE KP; SEMMELMAYER U et al.1974; MONATSSCHR. KINDERHEILKDE; DTSCH.; DA. 1974; VOL. 122; NO 6; PP. 337-342; ABS. ANGL.; BIBL. 3REF.Article

AN UNUSUAL PARTIAL TRISOMY 13STOLL C; MESSER J; WEITZENBLUM S et al.1976; CLIN. GENET.; DENM.; DA. 1976; VOL. 9; NO 1; PP. 1-4; BIBL. 5 REF.Article

A (13;22) ROBERTSONIAN TRANSLOCATION, 45 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-392ALFI O; MILLER RC; GREENE AE et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 15; NO 1; PP. 55-56Article

RECURRENT ABORTIONS AND PATERNAL BALANCED TRANSLOCATION T (1Q-; 13Q+). = AVORTEMENTS RECURRENTS ET TRANSLOCATION BALANCEE T(1Q-; 13Q+) CHEZ LE PEREROZYNKOWA D; TREBICKA KWIATKOWSKA B; STEPIEN J et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 4; PP. 349-351; BIBL. 7 REF.Article

TRANSLOCATION T(7 P+;13Q-) ASSOCIATED WITH RECURRENT ABORTION. = TRANSLOCATION T(7P+;13Q-) AVEC AVORTEMENTS A REPETITIONKORNER H; AGRICOLA H; BAYER H et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 28; NO 1; PP. 83-86; BIBL. 6 REF.Article

A CASE OF (9P+,13Q-) TRANSLOCATION. CYTOGENETICS AND FAMILY HISTORYJOTTERAND M; CATTI A; JUILLARD E et al.1975; ARCH. GENET.; SCHWEIZ; DA. 1975; VOL. 48; NO 1; PP. 75; (SCHWEIZ. GES. GENET. JAHRESVERSAMML. ZUSAMMENFASSUNGEN REFRATE; LAUSANNE; 1974)Conference Paper

ELIMINATION OF NUCLEOLUS ORGANIZERS IN A CASE OF 13/14 ROBERTSONIAN TRANSLOCATION.HURLEY JE; PATHAK S.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 35; NO 2; PP. 169-173; BIBL. 10 REF.Article

TWO CASES OF 8P TRISOMY IN ONE SIBSHIP = DEUX CAS DE TRISOMIE 8P DANS UNE FRATRIECHIYO HA; NAKAGOME Y; MATSUI I et al.1975; CLIN. GENET.; DENM.; DA. 1975; VOL. 7; NO 4; PP. 328-333; BIBL. 18REF.Article

CHROMOSOME ANOMALIES IN THREE SUCCESSIVE ABORTUSES DUES TO PATERNAL TRANSLOCATION, T (13Q-18Q+)KAJII T; MEYLAN J; MIKAMO K et al.1974; CYTOGENET. CELL GENET.; SWITZ.; DA. 1974; VOL. 13; NO 5; PP. 426-436; BIBL. 1 P. 1/2Article

FAMILIAL C/D TRANSLOCATION T(9;13) (9P23; 13Q21) IN A MALE ASSOCIATED WITH RECURRENT ABORTION.PAL SINGH KAHLON D; SERRA A.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 3; PP. 223-230; BIBL. 1 P. 1/2Article

Q-SYNDROME: FAMILY STUDY.CARMICHAEL A; ADDY DP; SHORTLAND WEBB WR et al.1977; ARCH. DIS. CHILDH.; G.B.; DA. 1977; VOL. 52; NO 12; PP. 972-974; BIBL. 8 REF.Article

PARTIAL TRISOMY 13Q INHERITED FROM BALANCED TRANSLOCATION (5; 13) (P14; Q13)COCO R; DEL REY G.1978; J. GENET. HUM.; CHE; DA. 1978; VOL. 26; NO 4; PP. 303-310; ABS. FRE/GER; BIBL. 6 REF.Article

RETINOBLASTOMA IN A PATIENT WITH A 13QXP TRANSLOCATION.CROSS HE; HANSEN RC; MORROW G III et al.1977; AMER. J. OPHTHALMOL.; U.S.A.; DA. 1977; VOL. 84; NO 4; PP. 548-554; BIBL. 35 REF.Article

INHERITED CHROMOSOMAL TRANSLOCATION IN TWO FAMILIES (T(4Q-; 13Q+) AND T(5Q-; 13Q+).WATANABE G; KIYOI Y; TAKEYAMA I et al.1977; TOHOKU J. EXPER. MED.; JAP.; DA. 1977; VOL. 121; NO 2; PP. 179-184; BIBL. 5 REF.Article

TRISOMIE PARTIELLE 18Q PAR TRANSLOCATION FAMILIALE T(18Q-; 13Q+)CASTEL Y; RIVIERE D; NAWROCKI T et al.1975; LYON MED.; FR.; DA. 1975; VOL. 233; NO 3; PP. 211-217; ABS. ANGL.; BIBL. 26REF.Article

TRANSLOCATION ROBERTSONIENNE 13.22 CHEZ LE PERE D'UN ENFANT ATTEINT DE TRISOMIE 21 LIBRE.WALBAUM R; DEROUBAIX P; VAN DE VELDE MF et al.1976; PEDIATRIE; FR.; DA. 1976; VOL. 31; NO 7; PP. 697-701; ABS. ANGL.; BIBL. 12 REF.Article

HEMIHYPOTROPHY IN A GIRL WITH A TRANSLOCATION T(13 Q; 7 P). = UNE HEMIATROPHIE CHEZ UNE FILLETTE PRESENTANT UNE TRANSLOCATION T(13 Q; 7 P)MARCALLO FA; WERNECK LC; PILOTTO RF et al.1977; EUROP. J. PEDIATR.; GERM.; DA. 1977; VOL. 124; NO 3; PP. 167-171; BIBL. 4 REF.Article

A NEW CASE OF TRISOMY FOR THE DISTAL PART OF 13Q DUE TO MATERNAL TRANSLOCATION, T(9;13) (P21;Q21).JOTTERAND M; JUILLARD E.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 3; PP. 213-222; BIBL. 20 REF.Article

PATAU'S SYNDROME AND 13Q 21Q TRANSLOCATION.PEREZ CASTILLO A; ABRISQUETA JA.1978; HUM. GENET.; DEU; DA. 1978; VOL. 42; NO 3; PP. 327-331; BIBL. 12 REF.Article

A CASE OF (13Q; 18Q) TRANSLOCATION WITH PROXIMAL 13Q MONOSOMY.SUZUKI Y; ONO K; OKA S et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 38; NO 3; PP. 337-341; BIBL. 5 REF.Article

SUCCESSIVE SPONTANEOUS ABORTIONS WITH DIVERSE CHROMOSOMAL ABERRATIONS IN HUMAN TRANSLOCATION HETEROZYGOTEKOHN G; ORNOY A; BEN TSUR Z et al.1975; TERATOLOGY; U.S.A.; DA. 1975; VOL. 12; NO 5; PP. 283-289; BIBL. 27 REF.Article

TRANSLOCATION 9Q/13Q RESULTING IN DUPLICATION (TRISOMY 9PTER->9Q22) AND DEFICIENCY (MONOSOMY 13PTER->13Q12).HOWARD PEEBLES PN; YARBROUGH KM; STODDARD GR et al.1977; CLIN. GENET.; DENM.; DA. 1977; VOL. 11; NO 1; PP. 46-52; BIBL. 20 REF.Article

VARIANT EXCEPTIONNEL D'UN CHROMOSOME 22. DEFINITION D'UNE ATTITUDE PRATIQUE.CAPET LE PORRIER N.1978; ; S.L.; DA. 1978; PP. 1-62; BIBL. 13 P. 1/2; (THESE DOCT. MED.; PARIS VI)Thesis

INHERITED PERICENTRIC INVERSION OF CHROMOSOME NO. 2 WITH ROBERTSONIAN TRANSLOCATION (13Q 14Q) RESULTING IN TRISOMY FOR CHROMOSOME 13Q.VERMA RS; DOSIK H; WEXLER IB et al.1977; J. GENET. HUM.; SUISSE; DA. 1977; VOL. 25; NO 4; PP. 295-301; ABS. FR. ALLEM.; BIBL. 1 P. 1/2Article

FAMILIAL TRANSLOCATION WITH PARTIAL TRISOMY OF 13 AND 22: EVIDENCE THAT SPECIFIC REGIONS OF CHROMOSOMES 13 AND 22 ARE RESPONSIBLE FOR THE PHENOTYPE OF EACH TRISOMY.KIM HJ; HSU LYF; GOLDSMITH LC et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 2; PP. 114-119; BIBL. 21 REF.Article

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