Quantification of sources of variation and accuracy of sequence discrimination in a replicated microarray experimentBROWN, J. Steven; KUHN, David; WISSER, Randall et al.BioTechniques. 2004, Vol 36, Num 2, pp 324-332, issn 0736-6205, 9 p.Article

Mobility-shift analysis with microfluidics chipsCLARK, Jarred; SHEVCHUK, Taras; SWIDERSKI, Piotr M et al.BioTechniques. 2003, Vol 35, Num 3, pp 548-554, issn 0736-6205, 7 p.Article

Non-random radial arrangements of interphase chromosome territories: evolutionary considerations and functional implicationsTANABE, Hideyuki; HABERMANN, Felix A; SOLOVEI, Irina et al.Mutation research. Fundamental and molecular mechanisms of mutagenesis. 2002, Vol 504, Num 1-2, pp 37-45, issn 1386-1964Conference Paper

The relationship between genotype and chromosome aberration frequencies in a normal adult populationPLUTH, J. M; NELSON, D. O; RAMSEY, M. J et al.Pharmacogenetics (London). 2000, Vol 10, Num 4, pp 311-319, issn 0960-314XArticle

Characterization of three hairy cell leukemia-derived cell lines (ESKOL, JOK-1, and Hair-M) by multiplex-FISH, comparative genomic hybridization, FISH, PRINS, and dideoxyPRINSANDERSEN, C. Lindbjerg; ØSTERGAARD, M; NIELSEN, B et al.Cytogenetics and cell genetics. 2000, Vol 90, Num 1-2, pp 30-39, issn 0301-0171Article

Clinical and molecular studies in 15 females with ring X chromosomes: implications for r(X) formation and mental developmentMATSUO, Mari; MUROYA, Koji; HANEW, Kunihiko et al.Human genetics. 2000, Vol 107, Num 5, pp 433-439, issn 0340-6717Article

The influence of interstitial telomeric sequences on chromosome instability in human cellsDESMAZE, C; ALBERTI, C; MARTINS, L et al.Cytogenetics and cell genetics. 1999, Vol 86, Num 3-4, pp 288-295, issn 0301-0171Article

Absence of selection against aneuploid mouse sperm at fertilizationMARCHETTI, F; LOWE, X; BISHOP, J et al.Biology of reproduction. 1999, Vol 61, Num 4, pp 948-954, issn 0006-3363Article

Sequences flanking the centromere of human chromosome 10 are a complex patchwork of arm-specific sequences, stable duplications and unstable sequences with homologies to telomeric and other centromeric locationsJACKSON, M. S; ROCCHI, M; MARZELLA, R et al.Human molecular genetics (Print). 1999, Vol 8, Num 2, pp 205-215, issn 0964-6906Article

Structural unbalanced chromosome rearrangements resolved by comparative genomic hybridizationDANIELY, M; BARKAI, G; GOLDMAN, B et al.Cytogenetics and cell genetics. 1999, Vol 86, Num 1, pp 51-55, issn 0301-0171Conference Paper

Short telomeres on human chromosome 17pMARTENS, U. M; ZIJLMANS, J. M. J. M; POON, S. S. S et al.Nature genetics. 1998, Vol 18, Num 1, pp 76-80, issn 1061-4036Article

Asynchronous replication of homologous α-satellite DNA loci in man is associated with nondisjunctionLITMANOVITCH, T; ALTARAS, M. M; DOTAN, A et al.Cytogenetics and cell genetics. 1998, Vol 81, Num 1, pp 26-35, issn 0301-0171Article

Chromosome painting : a useful artRIED, T; SCHRÖCK, E; YI NING et al.Human molecular genetics (Print). 1998, Vol 7, Num 10, pp 1619-1626, issn 0964-6906Article

Cytogenetic analysis using simultaneous and sequential fluorescence in situ hybridizationESCUDERO, T; FUSTER, C; COLL, M. D et al.Cancer genetics and cytogenetics. 1998, Vol 100, Num 2, pp 111-113, issn 0165-4608Article

Increased rate of nondisjunction in sex cells derived from low-quality semenFINKELSTEIN, S; MUKAMEL, E; YAVETZ, H et al.Human genetics. 1998, Vol 102, Num 2, pp 129-137, issn 0340-6717Article

Automated selection of short tandem repeat polymorphism markers for whole genome screening for segmental aneusomyBIESECKER, L. G; SCHÄFFER, A. A.Human heredity. 1997, Vol 47, Num 2, pp 76-85, issn 0001-5652Article

Detection of chromosomal alterations affecting the 1cen-1q12 region in irradiated granulocytes and lymphocytes by multicolour FISH with tandem DNA probesRUPA, D. S; HASEGAWA, L. S; EASTMOND, D. A et al.Mutagenesis. 1997, Vol 12, Num 4, pp 195-200, issn 0267-8357Article

Incidence of chromosome 1 disomy in human sperm estimated by the primed in situ (PRINS) labeling techniquePELLESTOR, F; GIRARDET, A; ANDREO, B et al.Cytogenetics and cell genetics. 1997, Vol 76, Num 3-4, pp 192-195, issn 0301-0171Article

Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35142 sperm nuclei from two 47,XYY malesCHEVRET, E; ROUSSEAUX, S; MONTEIL, M et al.Human genetics. 1997, Vol 99, Num 3, pp 407-412, issn 0340-6717Article

Methods for improving the yield and quality of metaphase preparations for FISH probing of human lymphocyte chromosomesMCFEE, A. F; SAYER, A. M; SALOMAA, S. I et al.Environmental and molecular mutagenesis (Print). 1997, Vol 29, Num 1, pp 98-104, issn 0893-6692Article

A stable marker chromosome with a cryptic centromere : evidence for centromeric sequences associated with an inverted duplicationSACCHI, N; MAGNANI, I; FUHRMAN-CONTI, A. M et al.Cytogenetics and cell genetics. 1996, Vol 73, Num 1-2, pp 123-129, issn 0301-0171Article

Activation status of the X chromosome in human micronucleated lymphocytesTUCKER, J. D; NATH, J; HANDO, J. C et al.Human genetics. 1996, Vol 97, Num 4, pp 471-475, issn 0340-6717Article

Breakpoint diversity illustrates distinct mechanisms for Robertsonian translocation formationPAGE, S. L; SHIN, J.-C; HAN, J.-Y et al.Human molecular genetics (Print). 1996, Vol 5, Num 9, pp 1279-1288, issn 0964-6906Article

Heterogeneity in telomere length of human chromosomesLANSDORP, P. M; VERWOERD, N. P; VAN DE RIJKE, F. M et al.Human molecular genetics (Print). 1996, Vol 5, Num 5, pp 685-691, issn 0964-6906Article

Inversion-subversion of short DNA sequences by a nuclear vesicle on a kinked chromatidMATIOLI, G. T.Medical hypotheses. 1996, Vol 46, Num 2, pp 116-118, issn 0306-9877Article