LOCALISATION PROBABLE DU GENE DE LA GLUTATHION REDUCTASE (EC 1.6.4.2) SUR LA BANDE 8 P 21.SINET PM; BRESSON JL; COUTURIER J et al.1977; ANN. GENET.; FR.; DA. 1977; VOL. 20; NO 1; PP. 13-17; ABS. ANGL.; BIBL. 17 REF.Article

Functional C8 associated with human plateletsTEDESCO, F; DENSEN, P; VILLA, M. A et al.Clinical and experimental immunology (Print). 1986, Vol 66, Num 2, pp 472-480, issn 0009-9104Article

DNA sequence and analysis of human chromosome 8NUSBAUM, Chad; MIKKELSEN, Tarjei S; CHANG, Jean L et al.Nature (London). 2006, Vol 439, Num 7074, pp 331-335, issn 0028-0836, 5 p.Article

KARYOTYPE-PHENOTYPE CORRELATION: MOSAIC TRISOMY 8 AND PARTIAL TRISOMIES OF DIFFERENT SEGMENTS OF CHROMOSOME 8.RICCARDI VM; CRANDALL BF; SCHINZEL A et al.1978; HUM. GENET.; GERM.; DA. 1978; VOL. 41; NO 3; PP. 363-367; BIBL. 17 REF.Article

SMALL STRUCTURAL CHANGES OF CHROMOSOME 8. TWO CASES WITH EVIDENCE FOR DELETION.BEIGHLE C; KARP LE; HANSON JW et al.1977; HUM. GENET.; GERM.; DA. 1977; VOL. 38; NO 1; PP. 113-121; BIBL. 1 P. 1/2Article

FAMILIAL INVERSION OF CHROMOSOME NO. 8. AN AFFECTED CHILD AND A CARRIER FETUS = INVERSION FAMILIALE DU CHROMOSOME NO 8. UN ENFANT ATTEINT ET UN FOETUS CONDUCTEURFUJIMOTO A; WILSON MG; TOWNER JW et al.1975; HUMANGENETIK; DTSCH.; DA. 1975; VOL. 27; NO 1; PP. 67-73; BIBL. 21REF.Article

Tricho-rhino-phalangeal syndrome type I (TRP I) due to an apparently balanced translocation involving 8q24MARCHAU, F. E; VAN ROY, B. C; PARIZEL, P. M et al.American journal of medical genetics. 1993, Vol 45, Num 4, pp 450-455, issn 0148-7299Article

Extremer Gewebe-Mosaizismus bei Trisomie 8-Syndrom Trisomie 8 in Fibroblasten bei normalem Karyotyp in Lymphozyten = Mosaïcisme tissulaire extrême dans le syndrome de trisomie 8. Trisomie 8 dans les fibroblastes avec caryotype normal dans les lymphocytesMEISEL-STOSIEK, M; PFEIFFER, R. A; TIETZE, H. U et al.Klinische Pädiatrie. 1983, Vol 195, Num 5, pp 365-368, issn 0300-8630Article

8q24.12 interstitial deletion in trichorhinophalangeal syndrome type IFRYNS, J. P; VAN DEN BERGHE, H.Human genetics. 1986, Vol 74, Num 2, pp 188-189, issn 0340-6717Article

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

INHERITED PARTIAL TRISOMY 8Q (22->QTER).TOWNES PL; WHITE MR.1978; AMER. J. DIS. CHILD.; U.S.A.; DA. 1978; VOL. 132; NO 5; PP. 498-501; BIBL. 20 REF.Article

Localization of the kappa opioid receptor gene to human chromosome band 8q11.2YASUDA, K; ESPINOSA, R. III; TAKEDA, J et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 3, pp 596-597, issn 0888-7543Article

Tetranucleotide repeat polymorphism at the D8S344 locusWARD, K; RILEY, R; LU, J et al.Human molecular genetics (Print). 1993, Vol 2, Num 7, issn 0964-6906, p. 1087Article

Regional localization of the gene for clusterin (SP-40,40;gene symbol CLI) to human chromosome 8p12→p21DIETZSCH, E; MURPHY, B. F; KIRSZBAUM, L et al.Cytogenetics and cell genetics. 1992, Vol 61, Num 3, pp 178-179, issn 0301-0171Article

The gene for human carbonic anhydrase II (CA2) is located at chromosome 8q22NAKAI, H; BYERS, M. G; VENTA, P. J et al.Cytogenetics and cell genetics. 1987, Vol 44, Num 4, pp 234-235, issn 0301-0171Article

Tissue-type plasminogen activator gene is on chromosome 8TRIPPUTI, P; BLASI, F; NY, T et al.Cytogenetics and cell genetics. 1986, Vol 42, Num 1-2, pp 24-28, issn 0301-0171Article

A (2; 8) TRANSLOCATION, 46 CHROMOSOMES. REPOSITORY IDENTIFICATION NO. 6M-327.WORTON RG; ARONSON MM; GREENE AE et al.1977; CYTOGENET. CELL GENET.; SWITZ.; DA. 1977; VOL. 18; NO 4; PP. 243Article

Molecular Characterization of an Atypical Inv Dup Del 8q. Proposal of a Mechanism of FormationRODRIGUEZ, Laura; NEVADO, Julián; VALLESPIN, Elena et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 4, pp 915-919, issn 1552-4825, 5 p.Article

Assignment of the gene for the cytochrome c₁ subunit of the mitochondrial cytochrome bc₁ complex (CYC1) to human chromosome 8q24.3DUNCAN, A. M. V; OZAWA, T; SUZUKI, H et al.Genomics (San Diego, Calif.). 1994, Vol 19, Num 2, pp 400-401, issn 0888-7543Article

Mapping of the bone morphogenetic protein 1 gene (BMP1) to 8p21 : removal of BMP1 from candidacy for the bone disorder in Langer-Giedion syndromeYOSHIURA, K; TAMURA, T; HONG, H.-S et al.Cytogenetics and cell genetics. 1993, Vol 64, Num 3-4, pp 208-209, issn 0301-0171Conference Paper

Structure and function of C8 in the membrane attack sequence of complementSODETZ, J. M.Current Topics in Microbiology and Immunology. 1989, Num 140, pp 19-31, issn 0070-217XArticle

The human neurofilament gene (NEFL) is located on the short arm of chromosome 8HURST, J; FLAVELL, D; JULIEN, J.-P et al.Cytogenetics and cell genetics. 1987, Vol 45, Num 1, pp 30-32, issn 0301-0171Article

Assignment of the gene for human DNA polymerase β (POLB) to chromosome 8MATSUKAGE, A; YAMAGUCHI, M; UTSUMI, K. R et al.Japanese journal of cancer research. 1986, Vol 77, Num 4, pp 330-333, issn 0910-5050Article

MAPPING OF THE GENE FOR GLUTATHIONE REDUCTASE ON CHROMOSOME 8.DE LA CHAPELLE A; ICEN A; AULA P et al.1976; ANN. GENET.; FR.; DA. 1976; VOL. 19; NO 4; PP. 253-256; ABS. FR.; BIBL. 14 REF.Article

Regional assignment of 64 human gene transcripts on chromosome 8UGOLINI, F; CHAFFANET, M; HOULGATTE, R et al.Cytogenetics and cell genetics. 1997, Vol 77, Num 3-4, pp 197-200, issn 0301-0171Article