Systematic search for major genes in Schizophrenia : methodological issues and results from chromosome 12DAWSON, E; POWELL, J. F; WHATLEY, S et al.American journal of medical genetics. 1995, Vol 60, Num 5, pp 424-433, issn 0148-7299Article

Assignment of apoptotic protease activating factor-1 gene (APAF1) to human chromosome band 12q23 by fluorescence in situ hybridizationKIM, H; JUNG, Y. K; KWON, Y. K et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 3-4, pp 252-253, issn 0301-0171Article

Assignment of the Rab13 gene (RAB13) to human chromosome band 12q13 by in situ hybridizationLEEK, J. P; HAMLIN, P. J; WILTON, J et al.Cytogenetics and cell genetics. 1997, Vol 79, Num 3-4, pp 210-211, issn 0301-0171Article

Assignment of human desert hedgehog gene (DHH) to chromosome band 12q13.1 by in situ hybridizationKAMISAGO, M; KIMURA, M; FURUTANI, Y et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 1-2, pp 117-118, issn 0301-0171Article

TRANSLOCATION T (2; 12) (P 25; Q21) CLASSEE D'ABORD COMME 2/XPASQUALI F; ZUFFARDI O; ZAMBONI G et al.1975; SEM. HOP., ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 1; PP. 64-66; ABS. ANGL.; BIBL. 12 REF.Article

AN (8; 12) TRANSLOCATION, BALANCED, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO GM-213LIN CC; UCHIDA I; HOTZ H et al.1975; CYTOGENET. CELL GENET.; SWITZ.; DA. 1975; VOL. 14; NO 1; PP. 78-79; BIBL. 1REF.Article

PARTIAL DELETION OF THE SHORT ARM OF CHROMOSOME 12 (P11;P13). REPORT OF A CASETENCONI R; BACCICHETTI C; ANGLANI F et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 95-98; ABS. FR.; BIBL. 13REF.Article

RING CHROMOSOME 12 AND LATENT CENTROMERESZUFFARDI O; DANESINO C; POLONI L et al.1980; CYTOGENET. CELL GENET.; ISSN 0301-0171; CHE; DA. 1980; VOL. 28; NO 3; PP. 151-157; BIBL. 24 REF.Article

The human 2', 5'-oligoadenylate synthetase-like gene (OASL) encoding the interferon-induced 56-kDa protein maps to chromosome 12q24.2 in the proximity of the 2', 5'-OAS locusHOVNANIAN, A; REBOUILLAT, D; LEVY, E. R et al.Genomics (San Diego, Calif.). 1999, Vol 56, Num 3, pp 362-363, issn 0888-7543Article

Mapping of the human PAWR (par-4) gene to chromosome 12q21JOHNSTONE, R. W; TOMMERUP, N; HANSEN, C et al.Genomics (San Diego, Calif.). 1998, Vol 53, Num 2, pp 241-243, issn 0888-7543Article

Report of the fourth international workshop on human chromosome 12 mapping, 1997KUCHERLAPATI, R; MARYNEN, P; TURC-CAREL, C et al.Cytogenetics and cell genetics. 1997, Vol 78, Num 2, pp 81-95, issn 0301-0171Article

CONTRIBUTION A L'ETUDE DE LA FAMILLE DES 2'-5' OLIGOADENYLATE SYNTHETASES = CHARACTERZATION OF cDNAs ENCODING HUMAN 2-5A SYNTHETASES AND HOMOLOGOUS PROTEINS AND THEIR CHROMOSOMAL LOCALIZATIONRebouillat, Dominique; Hovanessian, Ara.1997, 250 p.Thesis

De novo inverted tandem duplication of the short arm of chromosome 12 in a patient with microblepharonTEKIN, Mustafa; JACKSON-COOK, Colleen; PANDYA, Arti et al.American journal of medical genetics. 2001, Vol 104, Num 1, pp 42-46, issn 0148-7299Article

Confirmation of the assignment of the Dombrock blood group locus (DO)to chromosome 12p: Narrowing the boundaries to 12p12.3-p13.2MAUTHE, J; COGHLAN, G; ZELINSKI, T et al.Vox sanguinis (Basel. 1956). 2000, Vol 79, Num 1, pp 53-56, issn 0042-9007Article

Localization of the human membrane type 4-matrix metalloproteinase gene (MMP17) to chromosome 12q24PUENTE, X. S; PENDAS, A. M; LLANO, E et al.Genomics (San Diego, Calif.). 1998, Vol 54, Num 3, pp 578-579, issn 0888-7543Article

Regional assignment of the human 4-hydroxyphenylpyruvate dioxygenase gene (HPD) to 12q24→qter by fluorescence in situ hybridizationSTENMAN, G; RÖIJER, E; RÜETSCHI, U et al.Cytogenetics and cell genetics. 1995, Vol 71, Num 4, pp 374-376, issn 0301-0171Conference Paper

Genomic organization and refined mapping of the human nuclear corepressor 2 (NCOR2)/ silencing mediator of retinoid and thyroid hormone receptor (SMRT) gene on chromosome 12q24.3JIANG, Q; GALIEGUE-ZOUITINA, S; ROUMIER, C et al.Cytogenetics and cell genetics. 2001, Vol 92, Num 3-4, pp 217-220, issn 0301-0171Article

Assignment of Desert Hedgehog (DHH) to human chromosome bands 12q12→q13.1 by in situ hybridizationTATE, G; SATOH, H; ENDO, Y et al.Cytogenetics and cell genetics. 2000, Vol 88, Num 1-2, pp 93-94, issn 0301-0171Article

Chromosomal mapping of human armadillo genes belonging to the p120^ctn/plakophilin subfamilyBONNE, S; VAN HENGEL, J; VAN ROY, F et al.Genomics (San Diego, Calif.). 1998, Vol 51, Num 3, pp 452-454, issn 0888-7543Article

Mapping of the human DNA primase 1 (PRIM1) to chromosome 12q13CLOUTIER, S; HAMEL, H; CHAMPAGNE, M et al.Genomics (San Diego, Calif.). 1997, Vol 43, Num 3, pp 398-401, issn 0888-7543Article

Report of the third international workshop on human chromosome 12 mapping 1995MARYNEN, P; KUCHERLAPATI, R.Cytogenetics and cell genetics. 1996, Vol 73, Num 1-2, pp 1-25, issn 0301-0171, 23 p.Article

TETRASOMY 12P PRESENTING WITH LONG APPENDIX: A PRENATAL CASEAYDIN, H; ARISOY, R; GECKINLI, B et al.Genetic counseling. 2013, Vol 24, Num 4, pp 439-440, issn 1015-8146, 2 p.Article

Intrachromosomal triplication 12p11.22-p12.3 and gonadal mosaicism of partial tetrasomy 12pECKEL, Heike; WIMMER, Rainer; VOLLETH, Marianne et al.American journal of medical genetics. Part A. 2006, Vol 140, Num 11, pp 1219-1222, issn 1552-4825, 4 p.Article

Absence of 12q21.2q22 deletions and subtelomeric rearrangements in cardiofaciocutaneous (CFC) syndrome patientsKAVAMURA, M. I; ZOLLINO, M; LECCE, R et al.American journal of medical genetics. 2003, Vol 119A, Num 2, pp 177-179, issn 0148-7299, 3 p.Article

Further evidence for a bipolar risk gene on chromosome 12q24 suggested by investigation of haplotype sharing and allelic association in patients from the Faroe IslandsDEGN, B; LUNDORF, M. D; WANG, A et al.Molecular psychiatry. 2001, Vol 6, Num 4, pp 450-455, issn 1359-4184Article