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Generation of mouse chromosome painting probes by DOP-PCR amplification of microdissected meiotic chromosomesXIAO, Y; DARROUDI, F; KUIPERS, A. G. J et al.Cytogenetics and cell genetics. 1996, Vol 75, Num 1, pp 63-66, issn 0301-0171Article

Structural organization of multiple alphoid subsets coexisting on human chromosomes 1, 4, 5, 7, 9, 15, 18, and 19FINELLI, P; ANTONACCI, R; MARZELLA, R et al.Genomics (San Diego, Calif.). 1996, Vol 38, Num 3, pp 325-330, issn 0888-7543Article

Susceptibility genes for nicotine dependence : a genome scan and followup in an independent sample suggest that regions on chromosomes 2, 4, 10, 16, 17 and 18 merit further studySTRAUB, R. E; SULLIVAN, P. F; NEALE, M. C et al.Molecular psychiatry. 1999, Vol 4, Num 2, pp 129-144, issn 1359-4184Article

Use of the primed in situ labelling (PRINS) technique for a rapid detection of chromosomes 13, 16, 18, 21, X and YPELLESTOR, F; GIRARDET, A; LEFORT, G et al.Human genetics. 1995, Vol 95, Num 1, pp 12-17, issn 0340-6717Article

The physical maps for sequencing human chromosomes 1, 6, 9, 10, 13, 20 and X : The human genomeBENTLEY, D. R; DELOUKAS, P; SCOTT, C. E et al.Nature (London). 2001, Vol 409, Num 6822, pp 942-943, issn 0028-0836Article

Initial genome scan of the NIMH genetics initiative bipolar pedigrees : Chromosomes 4, 7, 9, 18, 19, 20, and 21qDETERA-WADLEIGH, S. D; BADNER, J. A; MAXWELL, M. E et al.American journal of medical genetics. 1997, Vol 74, Num 3, pp 254-262, issn 0148-7299Article

Human thymosin-β4/6-26 gene is part of a multigene family composed of seven members located on seven different chromosomesCLAUSS, I. M; WATHELET, M. G; SZPIRER, J et al.Genomics (San Diego, Calif.). 1991, Vol 9, Num 1, pp 174-180, issn 0888-7543, 7 p.Article

Cytogenetics of human brain tumorsBIGNER, S. H; MARK, J; BIGNER, D. D et al.Cancer genetics and cytogenetics. 1990, Vol 47, Num 2, pp 141-154, issn 0165-4608Article

Multiple polysomies in breast carcinomas : Preferential gain of chromosomes 1, 5, 6, 7, 12, 16, 17, 18, and 19ADEYINKA, A; MERTENS, F; IDVALL, I et al.Cancer genetics and cytogenetics. 1999, Vol 111, Num 2, pp 144-148, issn 0165-4608Article

Mitomycin C-induced mosaicism in C-band regions of human chromosomes 1, 9, 16, and YSIMI, S.Human genetics. 1985, Vol 70, Num 3, pp 243-245, issn 0340-6717Article

Chromosomal analysis of colonic adenomatous polypsLONGY, M; SAURA, R; SCHOULER, L et al.Cancer genetics and cytogenetics. 1990, Vol 49, Num 2, pp 249-257, issn 0165-4608Article

Initial genome screen for bipolar disorder in the NIMH Genetics Initiative pedigrees : Chromosomes 2, 11, 13, 14, and XSTINE, O. C; MCMAHON, F. J; REICH, T et al.American journal of medical genetics. 1997, Vol 74, Num 3, pp 263-269, issn 0148-7299Article

Four paralogous protein 4.1 genes map to distinct chromosomes in mouse and humanPETERS, L. L; WEIER, H.-U. G; WALENSKY, L. D et al.Genomics (San Diego, Calif.). 1998, Vol 54, Num 2, pp 348-350, issn 0888-7543Article

Linkape maps of rat chromosomes 15, 16, 17, 19, and XYING DU; REMMERS, E. F; GOLDMUNTZ, E. A et al.Genomics (San Diego, Calif.). 1996, Vol 32, Num 1, pp 113-116, issn 0888-7543Article

Chromosomal mapping of A1 and A2 adenosine receptors, VIP receptor, and a new subtype of serotonin receptorLIBERT, F; PASSAGE, E; PARMENTIER, M et al.Genomics (San Diego, Calif.). 1991, Vol 11, Num 1, pp 225-227, issn 0888-7543, 3 p.Article

La Mitomycine C induit des changements structuraux au niveau de l'hétérochromatine des chromosomes humains 1, 9, 16 et YMALYGINA, N. A; REMIZOVA, O. G; AKIF'EV, A. P et al.Citologiâ. 1988, Vol 30, Num 11, pp 1350-1354, issn 0041-3771Article

Balanced Transmission of a Paternal Complex Chromosomal Rearrangement Involving Chromosomes 2, 3, and 18BASINKO, Audrey; PERRIN, Aurore; FEREC, Claude et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 10, pp 2646-2650, issn 1552-4825, 5 p.Article

Human chromosome-specific DNA libraries: construction and purity analysisFUSCOE, J. C; MCNINCH, J. S; COLLINS, C. C et al.Cytogenetics and cell genetics. 1989, Vol 50, Num 4, pp 211-215, issn 0301-0171Article

Balanced double complex translocations [46,XX,t(1p;6p;7p;3q;11p)(11q;22p;21q)] in an infant with multiple congenital anomaliesFUKUSHIMA, Y; KUROKI, Y; ITO, T et al.American journal of medical genetics. 1986, Vol 25, Num 2, pp 313-317, issn 0148-7299Article

Chromosomal assignment of 14 genomic probes for highly polymorphic lociCOHEN-HAGUENAUER, O; NGUYEN VAN CONG; KNOWLTON, R. G et al.Cytogenetics and cell genetics. 1989, Vol 50, Num 2-3, pp 78-83, issn 0301-0171Article

No evidence of uniparental disomy 2, 6, 14, 16, 20, and 22 as a major cause of intrauterine growth retardationKOTZOT, D; LURIE, I. W; MEHES, K et al.Clinical genetics. 2000, Vol 58, Num 3, pp 177-180, issn 0009-9163Article

β satellite DNA : characterization and localization of two subfamilies from the distal and proximal shorts arms of the human acrocentric chromosomesGREIG, G. M; WILLARD, H. F.Genomics (San Diego, Calif.). 1992, Vol 12, Num 3, pp 573-580, issn 0888-7543Article

Implications of Prenatal Diagnosis of the Fetus With Both Interstitial Deletion and a Small Marker Ring Originating From Chromosome 5OHASHI, Hiroyasu; SUZUMORI, Kaoru; CHISAKA, Yasushi et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 1, pp 192-196, issn 1552-4825, 5 p.Article

A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26 and 16p13.3EWALD, H; FLINT, T; KRUSE, T. A et al.Molecular psychiatry. 2002, Vol 7, Num 7, pp 734-744, issn 1359-4184, 11 p.Article

Chronic myelogenous leukemia with t(9;22) and t(8;11): a new chromosome anomalyLAI, J.-L; JOUET, J.-P; SAVARY, J.-B et al.Cancer genetics and cytogenetics. 1987, Vol 25, Num 1, pp 103-107, issn 0165-4608Article

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