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

TRISOMIE PARTIELLE 12 ET 8 EN MOSAIQUE, AVEC TRANSLOCATION T(8;12)(P21;Q13).SAVARY JB; COUSIN J; LAI JL et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 2; PP. 122-127; ABS. ANGL.; BIBL. 14 REF.Article

Lethal presentation of mosaic tetrasomy 12p Pallister-Killian/syndromeYOUNG, I. D; DUCKETT, D. P; O'REILLY, K. M et al.Annales de génétique (Paris). 1989, Vol 32, Num 1, pp 62-64, issn 0003-3995, 3 p.Article

PTER->12P 12.2: POSSIBLE ASSIGNMENT OF HUMAN TRIOSE PHOSPHATE ISOMERASE.RETHORE MO; KAPLAN JC; JUNEN C et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 36; NO 2; PP. 235-237; BIBL. 8 REF.Article

SYNDROME +12P. CASE REPORT AND REVIEW.TENCONI R; PIOVAN E; PRETO A et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 39; NO 1; PP. 97-101; BIBL. 10 REF.Article

Deletion (12) (q 15 q 21.2)WATSON, M. S; MCALLISTER-BARTON, L; MAHONEY, M. J et al.Journal of medical genetics. 1989, Vol 26, Num 5, pp 343-344, issn 0022-2593, 2 p.Article

Fragile site in chromosome 12 in a patient with two miscarriagesSTETTEN, G; SROKA, B; NORBURY-GLASER, M et al.American journal of medical genetics. 1988, Vol 31, Num 3, pp 521-525, issn 0148-7299Article

The gene for the major intrinsic protein (MIP) of the ocular lens is assigned to human chromosome 12cen-q14SPARKES, R. S; MOHANDAS, T; HEINZMANN, C et al.Investigative ophthalmology & visual science. 1986, Vol 27, Num 9, pp 1351-1354, issn 0146-0404Article

LA TRISOMIE PARTIELLE DU BRAS COURT DU CHROMOSOME 12MEYER JEANNE.sd; FRA; METZ: DACTYLOGR. DUPLICATION ET RELIURE; DA. S.D.; 363; 86 P.: ILL.; 30 CM; BIBL. 7 P.; TH.: MED./NANCY 1/1978Thesis

TWO CASES OF TRISOMY 12P DUE TO 2CPT (12; 21) (P11; P11) INHERITED THROUGH THREE GENERATIONSPARSLOW M; CHAMBERS D; DRUMMOND M et al.1979; HUM. GENET.; DEU; DA. 1979; VOL. 47; NO 3; PP. 253-260; BIBL. 18 REF.Article

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

In situ hybridisation localises the gene for the major intrinsic protein of eye lens fibre cell membranes to human chromosome 12q14GRIFFIN, C. S; SHIELS, A.Cytogenetics and cell genetics. 1992, Vol 61, Num 1, pp 8-9, 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

Mapping of the immune interferon gamma gene (IFNG) to chromosome band 12q14 by fluorescence in sity hybridizationZIMONJIC, D. B; REZANKA, L. J; EVANS, C. H et al.Cytogenetics and cell genetics. 1995, Vol 71, Num 3, pp 247-248, issn 0301-0171Article

Regional localization of the gene coding for human brain nitric oxide synthase (NOS1) to 12q24.2→24.31 by fluorescent in situ hybridizationWEIMING XU; GORMAN, P; SHEER, D et al.Cytogenetics and cell genetics. 1993, Vol 64, Num 1, pp 62-63, issn 0301-0171Article

Regional assignment of the human keratin 5 (KRT5) gene to chromosmone 12q near D12S14 by PCR analysis of somatic cell hybrids and multicolor in situ hybridizationBONIFAS, J. M; BARE, J. W; LYNCH, E. D et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 2, pp 452-454, issn 0888-7543Article

Mapping of the human gene for a melanocyte protein Pmel 17 (D12S53E) to chromosome 12q13-q14KUBOTA, R; YIMIN WANG; MINOSHIMA, S et al.Genomics (San Diego, Calif.). 1995, Vol 26, Num 2, pp 430-431, issn 0888-7543Article

Localization of the human Sp1 transcription factor gene to 12q13 by fluorescence in situ hybridizationMATERA, A. G; WARD, D. C.Genomics (San Diego, Calif.). 1993, Vol 17, Num 3, pp 793-794, issn 0888-7543Article

Isolation and mapping of a polymorphic DNA sequence (pTHIZ53) on chrosomome 12 [D12S18]HOLM, T; NAKAMURA, Y; GILLILAN, S et al.Nucleic acids research. 1988, Vol 16, Num 12, issn 0305-1048, 5701Article

An unusual chromosome aberration 47,XX,+21,dup(12)(q13→q24),dup(12)(q13→q24) in a girl with down syndrome and acute monocytic leukemiaSODERHALL, S; ISELIUS, L; BJORK, O et al.Cancer genetics and cytogenetics. 1991, Vol 55, Num 1, pp 97-100, issn 0165-4608Article

Interphase fluorescence in situ hybridization for trisomy 12 on archival ovarian sex cord-stromal tumorsVANDANA SHASHI; GOLDEN, W. L; VON KAP-HERR, C et al.Gynecologic oncology (Print). 1994, Vol 55, Num 3, pp 349-354, issn 0090-8258, 1Article

Localization of the human salivary protein complex (SPC) to chromosome band 12p13.2MAMULA, P. W; HEEREMA, N. A; PALMER, C. G et al.Cytogenetics and cell genetics. 1985, Vol 39, Num 4, pp 279-284, issn 0301-0171Article

La monosomie partielle du bras court du chromosome 12: au sujet d'une observation = The 12p partial monosomy: one caseBOILLY DARTIGALONGUE, B; PARENT, P; TOUDIC, L et al.Revue internationale de pédiatrie. 1985, Num 149, pp 5-10, issn 0048-8135Article

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