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Results 1 to 25 of 920

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Intensity heteromorphisms of human chromosomes 15p by DA/DAPI techniqueBABU, A; MACERA, M. J; VERMA, R. S et al.Human genetics. 1986, Vol 73, Num 4, pp 298-300, issn 0340-6717Article

TRANSLOCATION D/D INVOLING TWO HOMOLOGOUS CHROMOSOMES OF THE PAIR 15.ZIZKA J; BALICEK P; FINKOVA A et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 1; PP. 123-125; BIBL. 4 REF.Article

TRISOMIE 15 PARTIELLE PROXIMALE. ASPECTS CYTOGENETIQUES ET CLINIQUES. ETUDE DE 2 NOUVELLES OBSERVATIONSMISSON FRANCK.1980; ; FRA; THIERS: IMPR. LE POINT; DA. 1980; 17; 165 P.-3 PL.: ILL.; 30 CM; H.T. 2; BIBL. 75 REF.; TH.: MED./CLERMONT 1/1980Thesis

/15 TRANSLOCATION IN PRADER-WILLI SYNDROME.FRACCARO M; ZUFFARDI O; BUHLER EM et al.1977; J. MED. GENET.; G.B.; DA. 1977; VOL. 14; NO 4; PP. 275-276; BIBL. 4 REF.Article

Discrepant results obtained with two versions of the farnsworth panel D-15 test in patients with acquired blue-yellow defectsPEASE, P. L.American journal of optometry and physiological optics. 1983, Vol 60, Num 9, pp 804-809, issn 0093-7002Article

Isolation and mapping of a polymorphic DNA sequence pMCT46.2 on chromosome 15 [D15S26]CARLSON, M; NAKAMURA, Y; KRAPCHO, K et al.Nucleic acids research. 1988, Vol 16, Num 3, issn 0305-1048, 1226Article

CONTRIBUTO ALLA PATOLOGIA DEL CROMOSOMA 22. = CONTRIBUTION A LA PATHOLOGIE DU CHROMOSOME 22GIORDANO A; GRIMOLDI MG; LAVEZZI AM et al.1976; FOLIA HERED. PATHOL.; ITAL.; DA. 1976; VOL. 25; NO 2; PP. 38-52; ABS. ANGL.; BIBL. 1 P. 1/2Article

CYTOGENETIC AND CLINICAL STUDIES IN FIVE CASES OF INV DUP(15)WISNIEWSKI L; HASSOLD T; HEFFELFINGER J et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 50; NO 3; PP. 259-270; BIBL. 2 P.Article

A (14; 15) ROBERTSONIAN TRANSLOCATION, 45 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. GM-479.GOLBUS MS; EPSTEIN CJ; ARONSON MM et al.1976; CYTOGENET. CELL GENET.; SWITZ.; DA. 1976; VOL. 17; NO 1; PP. 61Article

Cytogenetic analysis of a human familial 15p+marker chromosomeVELAZQUEZ, M; VISEDO, G; LUDENA, P et al.Genome (Ottawa. Print). 1991, Vol 34, Num 5, pp 827-829, issn 0831-2796Article

De novo partial trisomy 15q (proximal type)HERWEIJER, T. J; OORTHUYS, J. W. E; LESCHOT, N. J et al.Journal of medical genetics. 1988, Vol 25, Num 4, pp 260-262, issn 0022-2593Article

ANALYSIS OF BANDING PATTERNS AND MOSAIC CONFIGURATIONS IN A CASE OF RING CHROMOSOME 15.SCHMID M; HENRICHS I; NESTLER H et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 289-299; BIBL. 30 REF.Article

Isolation and mapping of a polymorphic DNA sequence pEKZ104.1 on chromosome 15 [15S30]KUMLIN-WOLFF, E; NAKAMURA, Y; MYERS, R et al.Nucleic acids research. 1988, Vol 16, Num 3, issn 0305-1048, 1224Article

PARTIAL TRISOMY OF CHROMOSOME 15.HOWARD PEEBLES PN; YARBROUGH K; STODDARD GR et al.1977; AMER. J. MENTAL DEFIC.; U.S.A.; DA. 1977; VOL. 81; NO 6; PP. 606-609; BIBL. 15 REF.Article

TWO CHILDREN WITH A PARTIAL TRISOMY OF CHROMOSOME 15 (47, XX, +15).PARKER CE; JAMSHED MAVALWALA; ALFI OS et al.1977; CLIN. PEDIATR.; U.S.A.; DA. 1977; VOL. 16; NO 11; PP. 1037-1041; BIBL. 25 REF.Article

RING CHROMOSOME 15 IN CHILD WITH A MINOR DYSMORPHISM OF PHENOTYPE.RUMENIE L; JOKSIMOVIC I; ANAF M et al.1976; HUM. GENET.; GERM.; DA. 1976; VOL. 33; NO 2; PP. 187-188; BIBL. 5 REF.Article

A potential rearrangement between CYP19 and TRPM7 genes on chromosome 15q21.2 as a cause of aromatase excess syndromeTIULPAKOV, Anatoly; KALINTCHENKO, Natalya; SEMITCHEVA, Tatyana et al.The Journal of clinical endocrinology and metabolism. 2005, Vol 90, Num 7, pp 4184-4190, issn 0021-972X, 7 p.Article

RFLP of the human c-fes proto-oncogeneTESCH, H; OLEK, K; GEISEL, J et al.Nucleic acids research. 1988, Vol 16, Num 9, issn 0305-1048, 4193Article

RING CHROMOSOME 15 SYNDROMEFRYNS JP; TIMMERMANS J; D'HONDT F et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 51; NO 1; PP. 43-48; BIBL. 9 REF.Article

De novo interstitial direct duplication of 15q:46, XY, dir dup (15) (pter→q24::q14→q21.1::q24→qter)HERR, H. M; SCOTT, C. I. JR; HORTON, S. J et al.Journal of medical genetics. 1983, Vol 20, Num 6, pp 473-475, issn 0022-2593Article

No evidence for DNA copy number change associated with the DUP25 cytogenetic phenotypeHOLLOX, Edward J; AL ARMOUR, John.European journal of human genetics. 2003, Vol 11, Num 12, pp 911-912, issn 1018-4813, 2 p.Article

B-cell lymphocytic lymphoma with circulating granular prolymphocytes and a novel trisomy 15 anomalyWONG, K. F; CHAN, J. K. C; KWONG, Y. L et al.Cancer genetics and cytogenetics. 1995, Vol 81, Num 1, pp 28-32, issn 0165-4608Article

CW15 : international workshop on human chromosome 15 mapping 1994MALCOLM, S; DONLON, T. A.Cytogenetics and cell genetics. 1994, Vol 67, Num 1, pp 1-22, issn 0301-0171Conference Proceedings

Regional localization of the gene for cardiac muscle actin (ACTC) on chromosome 15qKRAMER, P. L; LUTY, J. A; LITT, M et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 3, pp 904-905, issn 0888-7543Article

Identification of a second human subtitlisin-like protease gene in the fes/fps region of chromosome 15KIEFER, M. C; TUCKER, J. E; JOH, R et al.DNA and cell biology. 1991, Vol 10, Num 10, pp 757-769, issn 1044-5498Article

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