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

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

POLYMORPHISMUS DES CHROMOSOMS N2.15 BEIM MENSCHEN = POLYMORPHISME DU CHROMOSOME 15 CHEZ L'HOMMESCHNEDL W; WACHTLER F; MUSIL R et al.1980; WIEN. KLIN. WOCHENSCHR.; ISSN 0043-5325; AUT; DA. 1980; VOL. 92; NO 21; PP. 761-764; ABS. ENG; BIBL. 19 REF.Article

Translocation (15;17) in a child with variant form of acute promyelocytic leukemia = Translocation (15; 17) chez un enfant présentant une variante de leucémie aiguë promyélocytairePRIETO, F; BADIA, L; CASTEL, V et al.Cancer genetics and cytogenetics. 1983, Vol 10, Num 1, pp 117-120, issn 0165-4608Article

POLYMORPHIC VARIANTS IN HUMAN CHROMOSOME 15CHEN TR; KAO ML; MARKS J et al.1981; AM. J. MED. GENET.; ISSN 0148-7299; USA; DA. 1981; VOL. 9; NO 1; PP. 61-66; BIBL. 45 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

INTERSTITIAL DELETION OF THE LONG ARM OF CHROMOSOME 15FRYNS JP; DE MUELENAERE A; VAN DEN BERGHE H et al.1982; ANN. GENET.; ISSN 0003-3995; FRA; DA. 1982; VOL. 25; NO 1; PP. 59-60; ABS. ENG; BIBL. 4 REF.Article

Prader-Willi syndrome and chromosome 15. A clinical discussion of 20 casesMATTEI, J. F; MATTEI, M. G; GIRAUD, F et al.Human genetics. 1983, Vol 64, Num 4, pp 356-362, issn 0340-6717Article

Mosaic and non-mosaic trisomy 15q2ORYE, E; LAUREYS, G; VERHAAREN, H et al.Annales de génétique (Paris). 1985, Vol 28, Num 1, pp 58-60, issn 0003-3995Article

HUMAN GENE MAPPING USING AND X/AUTOSOME TRANSLOCATION.SOLOMON E; BOBROW M; GOODFELLOW PN et al.1976; SOMAT. CELL GENET.; U.S.A.; DA. 1976; VOL. 2; NO 2; PP. 125-140; BIBL. 28 REF.Article

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

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

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

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

Chromosomal sublocalization of human c-myb and c-fes cellular onc genes = Sublocalisation chromosomique des oncogènes cellulaires humains c-myb et c-fesHARPER, M. E; FRANCHINI, G; LOVE, J et al.Nature (London). 1983, Vol 304, Num 5922, pp 169-171, issn 0028-0836Article

MOSAICISME CHROMOSOMIQUE DANS LE SYNDROME DU 15 EN ANNEAUMALYGINA NA; MUTOVIN GR; FILINA NP et al.1980; GENETIKA; ISSN 0016-6758; SUN; DA. 1980; VOL. 16; NO 11; PP. 2029-2033; H.T. 2; ABS. ENG; BIBL. 12 REF.Article

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

Single nucleotide dimorphism in the transcribed region of the SNRPN gene at 15q12GIACALONE, J; FRANCKE, U.Human molecular genetics (Print). 1994, Vol 3, Num 2, issn 0964-6906, p. 379Article

Somatic cell mapping of the human cyclophilin B gene (PPIB) to chromosome 15PEDDADA, L. B; MCPHERSON, J. D; LAW, R et al.Cytogenetics and cell genetics. 1992, Vol 60, Num 3-4, pp 219-221, issn 0301-0171Conference Paper

Isolation and mapping of a polymorphic DNA sequence (pMCA1-1) on chromosome 15 [D15S33]CARLSON, M; NAKAMURA, Y; SARGEANT, L et al.Nucleic acids research. 1988, Vol 16, Num 3, issn 0305-1048, 1225Article

Organization of a repetitive human 1.8 kb KpnI sequence localized in the heterochromatin of chromosome 15HIGGINS, M. J; WANG, H; SHTROMAS, I et al.Chromosoma (Berlin. Print). 1985, Vol 93, Num 1, pp 77-86, issn 0009-5915Article

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

ASSIGNMENT OF THE SORBITOL DEHYDROGENASE LOCUS TO HUMAN CHROMOSOME 15 PTER->Q21DONALD LJ; WANG HS; HAMERTON JL et al.1980; BIOCHEM. GENET.; ISSN 0006-2928; USA; DA. 1980; VOL. 18; NO 5-6; PP. 425-431; BIBL. 11 REF.Article

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

Deletion of chromosome 15(q11-13) in a Prader-Labhart-Willi syndrome clinic populationCASSIDY, S. B; THULINE, H. C; HOLM, V. A et al.American journal of medical genetics. 1984, Vol 17, Num 2, pp 485-495, issn 0148-7299Article