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Non-disjunction of chromosome 13BUGGE, Merete; COLLINS, Andrew; TRANEBJAERG, Lisbeth et al.Human molecular genetics (Print). 2007, Vol 16, Num 16, pp 2004-2010, issn 0964-6906, 7 p.Article

Loci at chromosomes 13, 19 and 20 influence age at natural menopauseSTOLK, Lisette; GUANGJU ZHAI; SORANZO, Nicole et al.Nature genetics. 2009, Vol 41, Num 6, pp 645-647, issn 1061-4036, 3 p.Article

Primed in situ labeling: Sensitivity and specificity for detection of α-satellite DNA in the centromere regions of chromosomes 13 and 21YANG, J; SCHWINGER, E; MENNICKE, K et al.Cytogenetics and cell genetics. 2001, Vol 95, Num 1-2, pp 28-33, issn 0301-0171Article

Integrative genomic analysis reveals distinct transcriptional and genetic features associated with chromosome 13 deletion in multiple myelomaAGNELLI, Luca; BICCIATO, Silvio; LOMBARDI, Luigia et al.Haematologica (Roma). 2007, Vol 92, Num 1, pp 56-65, issn 0390-6078, 10 p.Article

A new neocentromere locus on chromosome 13 resulting in mosaic tetrasomy for distal 13q and an asymmetric phenotypeBARWELL, Julian; MAZZASCHI, Roberto; BINT, Sue et al.American journal of medical genetics. 2004, Vol 130A, Num 3, pp 295-298, issn 0148-7299, 4 p.Article

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Extramammary myofibroblastoma is genetically related to spindle cell lipomaMAGGIANI, Francesca; DEBIEC-RYCHTER, Maria; VERBEECK, Guy et al.Virchows Archiv. 2006, Vol 449, Num 2, pp 244-247, issn 0945-6317, 4 p.Article

Phenotype and 244k Array-CGH Characterization of Chromosome 13q Deletions : An Update of the Phenotypic Map of 13q21.1-qterKIRCHHOFF, Maria; BISGAARD, Anne-Marie; FAGERBERG, Christina et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 5, pp 894-905, issn 1552-4825, 12 p.Article

Identification of a male schizophrenic patient carrying a de novo balanced translocation, t(4;13)(p16.1; q21.31)ITOKAWA, Masanari; KASUGA, Takehiko; YOSHIKAWA, Takeo et al.Psychiatry and clinical neurosciences (Carlton. Print). 2004, Vol 58, Num 3, pp 333-337, issn 1323-1316, 5 p.Article

Assignment¹ of the Centromere Protein H (Cenph) gene to mouse chromosome band 13D1 by in situ hybridization and interspecific backcross analysesLO, A. W. I; LONGMUIR, D. F. S; FOWLER, K. J et al.Cytogenetics and cell genetics. 2000, Vol 90, Num 1-2, pp 56-57, issn 0301-0171Article

Physical and genetic localization of the gene encoding the AP-2 transcription factor to mouse chromosome 13WARREN, G; GORDON, M; SIRACUSA, L. D et al.Genomics (San Diego, Calif.). 1996, Vol 31, Num 2, pp 234-237, issn 0888-7543Article

Lgn1, a gene that determines susceptibility to Legionella pneumophila, maps to mouse chromosome 13DIETRICH, W. F; DAMRON, D. M; ISBERG, R. R et al.Genomics (San Diego, Calif.). 1995, Vol 26, Num 3, pp 443-450, issn 0888-7543Article

Implication of chromosome 13 on hypertension and associated disorders in Lyon hypertensive ratsGILIBERT, Sophie; BATAILLARD, Alain; NUSSBERGER, Juerg et al.Journal of hypertension. 2009, Vol 27, Num 6, pp 1186-1193, issn 0263-6352, 8 p.Article

Comparison of human chromosome 6p25 with mouse chromosome 13 reveals a greatly expanded ov-serpin gene repertoire in the mouseKAISERMAN, Dion; KNAGGS, Susan; REMOLD-O'DONNELL, Eileen et al.Genomics (San Diego, Calif.). 2002, Vol 79, Num 3, pp 349-362, issn 0888-7543Article

The gene for calcium-modulated cyclophilin ligand (CAMLG) is located on human chromosome 5q23 and a syntenic region of mouse chromosome 13BRAM, R. J; VALENTINE, V; SHAPIRO, D. N et al.Genomics (San Diego, Calif.). 1996, Vol 31, Num 2, pp 257-260, issn 0888-7543Article

Alignment of two genetic linkage maps on porcine chromosome 13DAVIES, W; HØYHEIM, B; SKOGTVEDT, S et al.Animal genetics (Print). 1995, Vol 26, Num 2, pp 119-121, issn 0268-9146Article

A radiation hybrid map of mouse chromosome 13ELLIOTT, R. W; MANLY, K. F; HOHMAN, C et al.Genomics (San Diego, Calif.). 1999, Vol 57, Num 3, pp 365-370, issn 0888-7543Article

Assignment1 of the ectodermal-neural cortex 1 gene (Enc1)to mouse chromosome band 13D1 by fluorescence in situ hybridizationHERNANDEZ, M.-C; ANDRES-BARQUIN, P. J; ISRAEL, M. A et al.Cytogenetics and cell genetics. 2000, Vol 89, Num 3-4, pp 158-159, issn 0301-0171Article

ANAL ATRESIA, ABNORMAL GENITALIA, AND ABSENT THUMB: CONGENITAL MALFORMATIONS ASSOCIATED WITH MOSAIC RING CHROMOSOME 13OCAK, Z; OZLU, T; VURAL, M et al.Genetic counseling. 2013, Vol 24, Num 2, pp 157-160, issn 1015-8146, 4 p.Article

13q13.1-q13.2 deletion in tetralogy of Fallot: Clinical report and a literature reviewCOSTAIN, Gregory; SILVERSIDES, Candice K; MARSHALL, Christian R et al.International journal of cardiology. 2011, Vol 146, Num 2, pp 134-139, issn 0167-5273, 6 p.Article

Umbilical Cord Ulceration after Prenatal Diagnosis of Duodenal Atresia with Interstitial Deletion of Chromosome 13q : A Case ReportMIYAKE, Hidehiko; YAMAMOTO, Akihito; TAKESHITA, Toshiyuki et al.Fetal diagnosis and therapy. 2008, Vol 24, Num 2, pp 115-118, issn 1015-3837, 4 p.Article

Loss of chromosome 13q is a frequently acquired event in genetic progression of soft tissue sarcomas in the abdominal cavityWENG, Wen-Hut; LERNER, Mikael; GRANDER, Dan et al.International journal of oncology. 2005, Vol 26, Num 1, pp 5-16, issn 1019-6439, 12 p.Article

THE EVOLUTION OF THE AMERICAN MAYDEAE. I. THE CHARACTERISTICS OF TWO TRIPSACUM CHROMOSOMES (TR 7 AND TR 13) THAT ARE PARTIAL HOMEOLOGS TO MAIZE CHROMOSOME 4RAO BGS; GALINAT WC.1974; J. HERED.; U.S.A.; DA. 1974; VOL. 65; NO 6; PP. 335-340; BIBL. 24 REF.Article

Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy numberHOGART, A; LEUNG, K. N; WANG, N. J et al.Journal of medical genetics. 2009, Vol 46, Num 2, pp 86-93, issn 0022-2593, 8 p.Article