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Assignment of Fgf12 to mouse chromosome bands 16B1 → B3 by in situ hybridizationHARTUNG, H; LOVEC, H; VERDIER, A.-S et al.Cytogenetics and cell genetics. 1997, Vol 76, Num 3-4, pp 185-186, issn 0301-0171Article

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Assignment of the gene for a ubiquitin fusion degradation protein (Ufd1l) to mouse chromosome 16B1-B4, syntenic with the Tuple1 geneBOTTA, A; JURECIC, V; PIZZUTI, A et al.Cytogenetics and cell genetics. 1997, Vol 77, Num 3-4, pp 264-265, issn 0301-0171Article

Chloride channel 2 gene (Clc2) maps to chromosome 16 of the mouse, extending a region of conserved synteny with human chromosome 3qLENGELING, A; GRONEMEIER, M; RONSIEK, M et al.Genetical research. 1995, Vol 66, Num 2, pp 175-178, issn 0016-6723Article

Localization of the giant axonal neuropathy gene to chromosome 16q24FLANIGAN, K. M; CRAWFORD, T. O; GRIFFIN, J. W et al.Annals of neurology. 1998, Vol 43, Num 1, pp 143-148, issn 0364-5134Article

Coexistence of inversion 16 and the Philadelphia chromosome comprising P190 BCR/ABL in chronic myeloid leukemia blast crisisNINOMIYA, Soranobu; KANEMURA, Nobuhiro; TSURUMI, Hisashi et al.International journal of hematology. 2011, Vol 93, Num 6, pp 806-810, issn 0925-5710, 5 p.Article

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A genome scan for Loci associated with aerobic running capacity in ratsWAYS, Justin A; CICILA, George T; GARRETT, Michael R et al.Genomics (San Diego, Calif.). 2002, Vol 80, Num 1, pp 13-20, issn 0888-7543Article

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

Biochemical characterization of bona fide polycystin-1 in vitro and in vivoBOLETTA, Alessandra; FENG QIAN; GERMINO, Gregory G et al.American journal of kidney diseases. 2001, Vol 38, Num 6, pp 1421-1429, issn 0272-6386Conference Paper

Genetics of allergic disease: Evidence for organ-specific susceptibility genesNISHIMURA, Akio; CAMPBELL-MELTZER, Robert Scott; CHUTE, Kathy et al.International archives of allergy and immunology. 2001, Vol 124, Num 1-3, pp 197-200, issn 1018-2438Conference Paper

Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies : Molecular mapping of a new syndrome by fluorescent in situ hybridization and microsatellites to 16q13 (D16S419-D16S503)STRATAKIS, Constantine A; LAFFERTY, Antony; TAYMANS, Susan E et al.The Journal of clinical endocrinology and metabolism. 2000, Vol 85, Num 9, pp 3396-3401, issn 0021-972XArticle

Deletion mapping of chromosome 16q in hepatocellular carcinomaPIAO, Z; PARK, C; KIM, J. J et al.British journal of cancer. 1999, Vol 80, Num 5-6, pp 850-854, issn 0007-0920Article

Characterization of the mouse Xpf DNA repair gene and differential expression during spermatogenesisSHANNON, M; LAMERDIN, J. E; RICHARDSON, L et al.Genomics (San Diego, Calif.). 1999, Vol 62, Num 3, pp 427-435, issn 0888-7543Article

Hemizygous deletions of chromosome band 16q24 in Wilms tumor : Detection by fluorescence in situ hybridizationSHEARER, P. D; VALENTINE, M. B; GRUNDY, P et al.Cancer genetics and cytogenetics. 1999, Vol 115, Num 2, pp 100-105, issn 0165-4608Article

Chromosome 16q24 deletion and decreased E-cadherin expression: Possible association with metastatic potential in prostate cancerYI PAN; MATSUYAMA, H; NAINING WANG et al.The Prostate. 1998, Vol 36, Num 1, pp 31-38, issn 0270-4137Conference Paper

Transient acute monoblastic leukemia with reciprocal (8;16)(p11;p13) translocationHEIM, S.Pediatric hematology and oncology. 1996, Vol 13, Num 3, pp 203-204, issn 0888-0018Article

Detection of allele loss on chromosome 16q in DNA isolated from fine needle aspiration specimens of breast tumors specimens of breast tumors. A simulation study using surgically resected specimensTSUDA, H; SAKAMAKI, C; SHIMAMURA, K et al.Acta cytologica. 1996, Vol 40, Num 4, pp 625-630, issn 0001-5547Conference Paper

Case of chronic eosinophilic leukemia with deletion of chromosome 16 and hepatitis CKAMINENI, Padma; BAPTISTE, Ayanna; HASSAN, Mukhtar et al.Journal of the National Medical Association. 2006, Vol 98, Num 8, pp 1356-1360, issn 0027-9684, 5 p.Article

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Haplotypes in the gene encoding protein kinase c-beta (PRKCB1) on chromosome 16 are associated with autismPHILIPPI, A; ROSCHMANN, E; MAILLARD, S et al.Molecular psychiatry. 2005, Vol 10, Num 10, pp 950-960, issn 1359-4184, 11 p.Article

Meta-analysis of four rheumatoid arthritis genome-wide linkage studies: Confirmation of a susceptibility locus on chromosome 16FISHER, S. A; LANCHBURY, J. S; LEWIS, C. M et al.Arthritis and rheumatism. 2003, Vol 48, Num 5, pp 1200-1206, issn 0004-3591, 7 p.Article

Genetic variation at the chromosome 16 chemokine gene cluster: Development of a strategy for association studies in complex diseaseFISHER, S. A; MOODY, A; LEWIS, C. M et al.Annals of human genetics. 2003, Vol 67, Num 5, pp 377-390, issn 0003-4800, 14 p.Article