[1] [Prenatal dystrophy]

[2] CAP3: A DNA sequence assembly program

[3] A role for the Smc3 hinge domain in the maintenance of sister chromatid cohesion

[4] Genome-wide mapping of the cohesin complex in the yeast Saccharomyces cerevisiae

[5] A polymorphic DNA marker genetically linked to Huntington's disease

[6] Comparison of extraintestinal pathogenic Escherichia coli strains from human and avian sources reveals a mixed subset representing potential zoonotic pathogens

[7] Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage

[8] Molecular analysis of the pathogenesis of beta-cell destruction in insulin-dependent diabetes mellitus

[9] The diploid genome sequence of an individual human

[10] In vivo analysis of chromosome condensation in Saccharomyces cerevisiae

[11] Senescence bypass screen identifies TBX2, which represses Cdkn2a (p19(ARF)) and is amplified in a subset of human breast cancers

[12] Chromosomal addresses of the cohesin component Mcd1p

[13] Eco1-dependent cohesin acetylation during establishment of sister chromatid cohesion

[14] A direct link between sister chromatid cohesion and chromosome condensation revealed through the analysis of MCD1 in S. cerevisiae

[15] In vivo requirements for rDNA chromosome condensation reveal two cell-cycle-regulated pathways for mitotic chromosome folding

[16] Cloning and chromosomal localization of the gene encoding human cyclin D-binding Myb-like protein (hDMP1)

[17] Cohesin-independent segregation of sister chromatids in budding yeast

[18] Identification of different regions among strains of Yersinia pestis by suppression subtractive hybridization

[19] ROCC, a conserved region in cohesin's Mcd1 subunit, is essential for the proper regulation of the maintenance of cohesion and establishment of condensation

[20] Pds5 is required for homologue pairing and inhibits synapsis of sister chromatids during yeast meiosis

[21] Polo kinase regulates mitotic chromosome condensation by hyperactivation of condensin DNA supercoiling activity

[22] Accurate whole human genome sequencing using reversible terminator chemistry

[23] Evolutionary expansion and divergence in the ZNF91 subfamily of primate-specific zinc finger genes

[24] Chromosomal rearrangement features of Yersinia pestis strains from natural plague foci in China

[25] Age-Related Loss of Cohesion: Causes and Effects

[26] Rheumatoid arthritis susceptibility loci at chromosomes 10p15, 12q13 and 22q13.

[27] Chromosome map of the Siamese cobra: did partial synteny of sex chromosomes in the amniote represent "a hypothetical ancestral super-sex chromosome" or random distribution?

[28] Engineering Synthetic Chromosomes by Sequential Loading of Multiple Genomic Payloads over 100 Kilobase Pairs in Size

[29] Little evidence for switches to environmental sex determination and turnover of sex chromosomes in lacertid lizards

[30] Sex chromosomes-linked single-gene disorders involved in human infertility

[31] Sequencing and Assembling Genomes and Chromosomes of Cereal Crops

[32] Analysis of chromosomes of embryos derived from translocation carriers during preimplantation genetic diagnosis cycles

[33] Clinical classification of 109 chronic myeloid leukemia cases and its correlation with Ph chromosomes

[34] Clinical classification of 109 chronic myeloid leukemia cases and its correlation with Ph chromosomes.

[35] Sex differences in kappa opioid receptor antinociception is influenced by the number of X chromosomes in mouse

[36] bloom’s syndrome: when chromosomes break

[37] y chromosomes of 40% chinese descend from three neolithic super-grandfathers.

[38] chromosomes of south american bufonidae (amphibia, anura) chromosomes of south american bufonidae (amphibia, anura)

[39] a high-density genetic map of wild emmer wheat from the karaca dağ region provides new evidence on the structure and evolution of wheat chromosomes

[40] aberrations in the chromosomes of cirrhinus mrigala (hamilton) upon exposure to butachlor

[41] comparative study of mitotic chromosomes in two blowflies, lucilia sericata and l. cluvia (diptera, calliphoridae), by c- and g-like banding patterns and rrna loci, and implications for karyotype evolution

[42] prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18

[43] comparative analysis of chromosomes in the palaearctic bush-crickets of tribe pholidopterini (orthoptera, tettigoniinae)

[44] patients with high-grade gliomas harboring deletions of chromosomes 9p and 10q benefit from temozolomide treatment

[45] gene mapping of 28s and 5s rdna sites in chromosomes of two barbus species and their f1 hybrids (teleostei, cyprinidae)

[46] split hand/foot malformations with microdeletions at chromosomes 7 and 19 detected using array comparative genomic hybridization

[47] prolactin and growth hormone affect metaphase-ii chromosomes in aging oocytes via cumulus cells using similar signaling pathways

[48] genes and chromosomes: control of development

[49] identifying parental chromosomes and genomic rearrangements in animal hybrid complexes of species with small genome size using genomic in situ hybridization (gish)

[50] embryonic hybrid cells: a powerful tool for studying pluripotency and reprogramming of the differentiated cell chromosomes

[51] chromatin organization by repetitive elements (core): a genomic principle for the higher-order structure of chromosomes

[52] RNF8 regulates active epigenetic modifications and escape gene activation from inactive sex chromosomes in post-meiotic spermatids

[53] Mismatch repair genes on chromosomes 2p and 3p account for a major share of hereditary nonpolyposis colorectal cancer families evaluable by linkage

[54] RNF8 regulates active epigenetic modifications and escape gene activation from inactive sex chromosomes in post-meiotic spermatids

[55] Mismatch Repair Genes on Chromosomes 2p and 3p Account for a Major Share of Hereditary Nonpolyposis Colorectal Cancer Families Evaluable by Linkage

[56] Fine-Mapping of Vitiligo Susceptibility Loci on Chromosomes 7 and 9 and Interactions with NLRP1 (NALP1)

[57] Modern alleles in archaic human Y chromosomes support origin of modern human paternal lineages in Asia rather than Africa