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Results 1 to 25 of 394

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TETRASOMY 9P: CLINICAL ASPECTS AND ENZYMATIC GENE DOSAGE EXPRESSIONGARCIA CRUZ D; VACA G; IBARRA B et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 4; PP. 237-242; ABS. FRE; BIBL. 12 REF.Article

THE TURNER PHENOTYPE AND THE DIFFERENT TYPES OF HUMAN X ISOCHROMOSOMEOTTO PG; VIANNA MORGANTE AM; OTTO PA et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 57; NO 2; PP. 159-164; BIBL. 32 REF.Article

HOW DO HUMAN ISOCHROMOSOMES ARISE.DE LA CHAPELLE A.1982; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1982; VOL. 5; NO 2; PP. 173-179; BIBL. 27 REF.Article

CYTOGENETIC INVESTIGATION OF SIX PATIENTS WITH X ISOCHROMOSOMES, I(XQ), AND OF TWO SUBJECTS WITH ISODICENTRIC X CHROMOSOMES, IDIC(XQ)GAAL M; LASZLO J; BOESZE P et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 4; PP. 362-365; BIBL. 22 REF.Article

DUPLICATION (17P) IN A CHILD WITH AN ISODICENTRIC (17P) CHROMOSOMEMASCARELLO JT; JONES MC; HOYME HE et al.1983; AMERICAN JOURNAL OF MEDICAL GENETICS; ISSN 0148-7299; USA; DA. 1983; VOL. 14; NO 1; PP. 67-72; BIBL. 10 REF.Article

THE ISOCHROMOSOME (179) IN CHRONIC MYELOCYTIC LEUKAEMIA: MECHANISM OF ORIGIN, CENTROMERIC FUNCTION AND CLONAL EVOLUTIONPASQUALI F; PANARELLO C; BERNASCONI P et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 1; PP. 89-90; BIBL. 11 REF.Article

ISOCHROMOSOME (17Q) IN PHILADELPHIA CHROMOSOME (PH1)-NEGATIVE JUVENILE CHRONIC MYELOCYTIC LEUKEMIACASALONE R; FRANCESCONI D; PASQUALI F et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 2; PP. 145-148; BIBL. 9 REF.Article

SEXUAL DEVELOPMENT OF PATIENTS WITH ISOCHROMOSOMES FOR THE LONG ARM OF THE X CHROMOSOMEHODGSON S; CHIU D; POLANI P et al.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 58; NO 2; PP. 176-178; BIBL. 13 REF.Article

RADIATION INDUCED PSEUDOISOCHROMOSOMES IN SUNNHEMP (CROTALASIA JUNCEA L)GUPTA PK; GUPTA R.1978; ACTA BOT. INDICA; IND; DA. 1978; VOL. 6; NO 1; PP. 31-35; BIBL. 6 REF.Article

THE TURNER PHENOTYPE AND THE DIFFERENT TYPES OF HUMAN X ISOCHROMOSOMELARIZZA D; ABBATI G; LORINI R et al.1982; HUMAN GENETICS; ISSN 0340-6717; DEU; DA. 1982; VOL. 62; NO 1; PP. 93; BIBL. 1 REF.Article

DICENTRIC ISOCHROMOSOME FOR THE LONG ARM OF CHROMOSOME 17, DIC I (17 Q), IN A PATIENT WITH CHRONIC MYELOGENOUS LEUKEMIA (CML)WHANG PENG J; LEE E; KNUTSEN T et al.1981; CANCER GENET. CYTOGENET.; ISSN 0165-4608; NLD; DA. 1981; VOL. 3; NO 3; PP. 233-236; BIBL. 18 REF.Article

POLYSOMY AND SUPERNUMERARY ISOCHROMOSOMES IN THE GRASSHOPPER OMOCESTUS BOLIVARI (CHOPARD)CAMACHO JPM; DIAZ DE LA GUARDIA R; RUIZ REJON M et al.1981; HEREDITY; ISSN 0018-067X; GBR; DA. 1981; VOL. 46; NO 1; PP. 123-126; BIBL. 10 REF.Article

CYTOGENETICS OF DISOMICS, MONOTELO- AND MONOISODISOMICS AND ML1 ST1 MUTANTS OF CHROMOSOME 4 OF COTTONENDRIZZI JE; BRAY R.1980; GENETICS; USA; DA. 1980; VOL. 94; NO 4; PP. 979-988; BIBL. 19 REF.Article

Un cas rare de mosaïcisme pour le chromosome 18 avec le caryotype 46, XX del (18) (p11)/46, XX, i (18 q)BADALYAN, L. O; MUTOVIN, G. R; MALYGINA, N. A et al.Genetika. 1983, Vol 19, Num 11, pp 1912-1915, issn 0016-6758Article

MILLEDGEVILLE MONGOLOID: A RARE KARYOTYPE OF DOWN' SYNDROMEJERNIGAN D; CURL N; KEELER C et al.1974; J. HERED.; U.S.A.; DA. 1974; VOL. 65; NO 4; PP. 254-257; BIBL. 21REF.Article

DIFFERENCES IN HUMAN X ISOCHROMOSOMESPRIEST JH; BLACKSTON RD; AU KS et al.1975; J. MED. GENET.; G.B.; DA. 1975; VOL. 12; NO 4; PP. 378-389; BIBL. 23 REF.Article

PSEUDO-ISOCHROMOSOMES IN PEARL MILLETSUKHA DEV P; MURTY JVVSN; MANGA V et al.1981; EXPERIENTIA; ISSN 0014-4754; CHE; DA. 1981; VOL. 37; NO 2; PP. 137; BIBL. 6 P.Article

Evolution of an octacentric isochromosome in mouse L-cellsVIG, B. K; ZINKOWSKI, R. P; MICHAELSON, D. S et al.Mutation research. 1984, Vol 128, Num 1, pp 41-45, issn 0027-5107Article

THREE PATIENTS WITH STRUCTURALLY ABNORMAL X CHROMOSOMES, EACH WITH XQ13 BREAKPOINTS AND A HISTORY OF IDIOPATHIC ACQUIRED SIDEROBLASTIC ANEMIADEWALD GW; PIERRE RV; PHYLIKY RL et al.1982; BLOOD; ISSN 0006-4971; USA; DA. 1982; VOL. 59; NO 1; PP. 100-105; BIBL. 22 REF.Article

RING-18 AND ISOPSEUDODICENTRIC-18 IN THE SAME CHILD: A HYPOTHESIS TO ACCOUNT FOR COMMON ORIGINMADAN K; VLASVELD L; BARTH PG et al.1981; ANN. GENET.; FRA; DA. 1981; VOL. 24; NO 1; PP. 12-16; ABS. FRE; BIBL. 37 REF.Article

ON THE SPECIFICITY OF MEDIUM-SIZED ISOMARKER CHROMOSOMES IN NON-BURKITT LYMPHOMAS.MARK J.1977; ACTA PATHOL. MICROBIOL. SCAND., A; DANEM.; DA. 1977; VOL. 85; NO 4; PP. 557-558; BIBL. 6 REF.Article

Tetrasomy 18p: Report of the Molecular and Clinical Findings of 43 IndividualsSEBOLD, Courtney; ROEDER, Elizabeth; O'DONNELL, Louise et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 9, pp 2164-2172, issn 1552-4825, 9 p.Article

PRESENCE OF H-Y ANTIGEN IN PATIENTS WITH ULLRICH-TURNER SYNDROME AND X-CHROMOSOME REARRANGEMENTSHASELTINE FP; DE PONTE KK; BREG WR et al.1982; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1982; VOL. 11; NO 1; PP. 97-107; BIBL. 1 P.Article

A CASE OF EDWARD'S SYNDROME WITH PSEUDODICENTRIC ISOCHROMOSOME 18: 46,XY,I DIC(18) (P11:P11)FIORETTI G; STABILE M; PAGANO L et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 2; PP. 116-118; ABS. FRE; BIBL. 13 REF.Article

PATERNAL OR MATERNAL ORIGIN OF HUMAN I(XQ) ISOCHROMOSOMESOTTO PA; OTTO PG.1981; HUM. GENET.; ISSN 0340-6717; DEU; DA. 1981; VOL. 59; NO 4; PP. 308-309; BIBL. 6 REF.Article

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