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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

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

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

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

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

Isolation and mapping of a polymorphic DNA sequence pYNZ90.1 on chromosome 15 [D15S28]NAKAMURA, Y; CULVER, M; KRAPCHO, K et al.Nucleic acids research. 1988, Vol 16, Num 2, issn 0305-1048, 780Article

Highly polymorphic locus D15S24 (CMW-1) maps to 15pter-q13. [HGM9 provisional no. D15S24]RICH, D. C; WITKOWSKI, C. M; SUMMERS, K. M et al.Nucleic acids research. 1988, Vol 16, Num 17, issn 0305-1048, 8740Article

Proximal 15q variant with normal phenotype in three unrelated individualsBROOKWELL, R; VELEBA, A.Clinical genetics. 1987, Vol 31, Num 5, pp 311-314, issn 0009-9163Article

A new location for the human adenine phosphoribosyltransferase gene (APRT) distal to the haptoglobin (HP) and fra(16)(q23) (FRA16D) lociFRATINI, A; SIMMERS, R. N; CALLEN, D. F et al.Cytogenetics and cell genetics. 1986, Vol 43, Num 1-2, pp 10-13, issn 0301-0171Article

Action de la mitomycine C sur les chromosomes humains et particulièrement sur les chromosomes acrocentriques = Effect of mitomycine C on human chromosomes and particulary on acrocentric chromosomesSOUIAH BELALEM, Nebia.1985, 56-[31] fThesis

Germline Mosacism in Shprintzen―Goldberg SyndromeSHANSKE, Alan L; GOODRICH, James T; ALA-KOKKO, Leena et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 7, pp 1574-1578, issn 1552-4825, 5 p.Article

Ring chromosome 15 : characterization by array CGHGLASS, Ian A; RAUEN, Katherine A; CHEN, Emily et al.Human genetics. 2006, Vol 118, Num 5, pp 611-617, issn 0340-6717, 7 p.Article

Association of deletions of the chromosomal region 15q24-ter and diaphragmatic hernia: A new case and discussion of the literatureHENGSTSCHLÄGER, Markus; MITTERMAYER, Christoph; REPA, Christa et al.Fetal diagnosis and therapy. 2004, Vol 19, Num 6, pp 510-512, issn 1015-3837, 3 p.Article

Assignment of an ionotropic glutamate receptor-like gene (GRINL1A) to human chromosome 15q22.1 by in situ hybridizationROGINSKI, R. S; MOHAN RAJ, B. K; FINKERNAGEL, S. W et al.Cytogenetics and cell genetics. 2001, Vol 93, Num 1-2, pp 143-144, issn 0301-0171Article

Delineation of a clinical syndrome caused by mosaic trisomy 15BÜHLER, E. M; BIENZ, G; STRAUMANN, E et al.American journal of medical genetics. 1996, Vol 62, Num 2, pp 109-112, issn 0148-7299Article

Dinucleotide repeat polymorphism at D15S221ALLAMAND, V; PEREIRA DE SOUZA, A; RICHARD, I et al.Human molecular genetics (Print). 1994, Vol 3, Num 2, issn 0964-6906, p. 382Article

Regional localization of human chromosome 15 lociRICHARD, I; BROUX, O; LORENZO, F et al.Genomics (San Diego, Calif.). 1994, Vol 23, Num 3, pp 619-627, issn 0888-7543Article

A specific phenotype associated with trisomy 15 mosaicismFRYNS, J. P; KLECZKOWSKA, A; LAGAE, L et al.Annales de génétique (Paris). 1993, Vol 36, Num 2, pp 129-131, issn 0003-3995Article