A nasty hex on chromosome 9 causes FTD/ALSCONNOLLY, C.Clinical genetics. 2012, Vol 81, Num 2, pp 126-127, issn 0009-9163, 2 p.Article

Assignment of tear lipocalin gene to human chromosome 9q34-9qterGLASGOW, B. J; HEINZMANN, C; KOJIS, T et al.Current eye research (Print). 1993, Vol 12, Num 11, pp 1019-1023, issn 0271-3683Article

Assignment of the BRCA1-associated RING domain gene (Bard1)to rat chromosome 9q34 by in situ hybridization and radiation hybrid mappingGRATAS, C; MEFLAH, K; HARB, J et al.Cytogenetics and cell genetics. 2001, Vol 94, Num 3-4, pp 250-251, issn 0301-0171Article

Assignment of TK1 encoding thymidine kinase to Syrian hamster chromosome 9 by microcell-mediated chromosome transferISLAM, K; ISLAM, M. Q.Cytogenetics and cell genetics. 1994, Vol 66, Num 3, pp 177-180, issn 0301-0171Article

Assignment of the gene coding for hepatocyte growth factor-like protein to mouse chromosome 9FRIEZNER DEGEN, S. J; GILBERT, D. J; JENKINS, N. A et al.Genomics (San Diego, Calif.). 1992, Vol 13, Num 4, pp 1368-1369, issn 0888-7543Article

Linkage analysis of the murine Hyal-1 locus on chromosome 9DE MAEYER-GUIGNARD, J; CACHARD-THOMAS, A; DE MAEYER, E et al.The Journal of experimental zoology. 1991, Vol 258, Num 2, pp 246-248, issn 0022-104X, 3 p.Article

The mouse orthologue of the human ionotropic glutamate receptor-like gene (GRINL1A) maps¹ to mouse chromosome 9WYDNER, K. S; MOHAN RAJ, B. K; SCIORRA, L. J et al.Cytogenetics and cell genetics. 2001, Vol 95, Num 3-4, pp 240-241, issn 0301-0171Article

Localization of the Tp53 gene on Syrian hamster chromosome 9 by fluorescence in situ hybridizationPOPESCU, N. C; ZIMONJIC, D. B; ALBOR, A et al.Cytogenetics and cell genetics. 1995, Vol 68, Num 1-2, pp 71-73, issn 0301-0171Article

A case of deletion of the short arm of chromosome 10 with severe hearing loss and brainstem dysfunctionKINOSHITA, Y; TANAKA, Y; YASUHARA, A et al.American journal of perinatology. 1992, Vol 9, Num 4, pp 299-301, issn 0735-1631Article

Trisomie 9 totale et homogène dépistée in utero = Complete trisomy 9 detected in uteroRAFFI, F; GENEIX, A; SATGE, D et al.Journal de gynécologie obstétrique et biologie de la reproduction. 1992, Vol 21, Num 2, pp 251-254, issn 0368-2315Article

Activating BRAF and N-Ras mutations in sporadic primary melanomas: an inverse association with allelic loss on chromosome 9KUMAR, Rajiv; ANGELINI, Sabrina; HEMMINKI, Kari et al.Oncogene (Basingstoke). 2003, Vol 22, Num 58, pp 9217-9224, issn 0950-9232, 8 p.Article

Assignment of five loci from human chromosome 8q onto sheep chromosome 9BROAD, T. E; BURKIN, D. J; CAMBRIDGE, L. M et al.Cytogenetics and cell genetics. 1995, Vol 68, Num 1-2, pp 102-106, issn 0301-0171Article

S-laminin : mapping to mouse chromosome 9 and expression in the linked mutants tippy and duckyPORTER, B. E; JUSTICE, M. J; COPELAND, N. G et al.Genomics (San Diego, Calif.). 1993, Vol 16, Num 1, pp 278-281, issn 0888-7543Article

A new locus for otosclerosis, OTSC8, maps to the pericentromeric region of chromosome 9INSAF BEL HADJ ALI; THYS, Melissa; SAIDA BEN ARAB et al.Human genetics. 2008, Vol 123, Num 3, pp 267-272, issn 0340-6717, 6 p.Article

Trisomy 9 mosaicism and XX sex reversalSOLOMON, Benjamin D; TURNER, Clesson E; KLUGMAN, Darren et al.American journal of medical genetics. Part A. 2007, Vol 143, Num 22, pp 2688-2691, issn 1552-4825, 4 p.Article

The paternal chromosome 9 and the maternal chromosome 22 are preferentially rearranged in chronic myeloid leukaemiaOLICIO, R; RIVERO, M. B; SEUANEZ, H. N et al.Leukemia. 2004, Vol 18, Num 8, pp 1445-1448, issn 0887-6924, 4 p.Article

Scn2b, a voltage-gated sodium channel β2 gene on mouse chromosome 9JONES, J. M; MEISLER, M. H; ISOM, L. L et al.Genomics (San Diego, Calif.). 1996, Vol 34, Num 2, pp 258-259, issn 0888-7543Article

Evidence for a thymus-affecting, recessive mouse gene (sty) located between the staggerer (sg) and short-ear (se) loci on chromosome 9HEINLEIN, U. A. O; WILLE, W.Cell biology international reports. 1992, Vol 16, Num 12, pp 1247-1250, issn 0309-1651Article

Chromosome 9 arm-specific telomere length and breast cancer riskZHENG, Yun-Ling; LOFFREDO, Christopher A; SHIELDS, Peter G et al.Carcinogenesis (New York. Print). 2009, Vol 30, Num 8, pp 1380-1386, issn 0143-3334, 7 p.Article

Chromosome 9 instability and alterations of p16 gene in squamous cell carcinoma of the lung and in adjacent normal bronchi : FISH and immunohistochemical studyDESSY, E; ROSSI, E; BERENZI, A et al.Histopathology. 2008, Vol 52, Num 4, pp 475-482, issn 0309-0167, 8 p.Article

Bladder neoplasms regions at chromosome 9 with putative tumour suppressor genesWADA, Takashi; BERGGREN, Petra; STEINECK, Gunnar et al.Scandinavian journal of urology and nephrology. 2003, Vol 37, Num 2, pp 106-111, issn 0036-5599, 6 p.Article

Autosomal aberrations associated with testicular dysgenesis or spermatogenic arrest in Chinese patientsGUO, Jin-Hu; ZHU, Pei-Yuan; HUANG, Yu-Feng et al.Asian journal of andrology. 2002, Vol 4, Num 1, pp 3-7, issn 1008-682XArticle

A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19BADENHOP, R. F; MOSES, M. J; SCIMONE, A et al.Molecular psychiatry. 2002, Vol 7, Num 6, pp 594-603, issn 1359-4184Article

Chromosome polysomy and histological characteristics in oral premalignant lesionsJIN KIM; SHIN, Dong M; EL-NAGGAR, Adel et al.Cancer epidemiology, biomarkers & prevention. 2001, Vol 10, Num 4, pp 319-325, issn 1055-9965Article

Genetic evidence for early divergence of small functioning and nonfunctioning endocrine pancreatic tumors: gain of 9Q34 is an early event in insulinomasSPEEL, Ernst J. M; SCHEIDWEILER, Alexander F; JIANMING ZHAO et al.Cancer research (Baltimore). 2001, Vol 61, Num 13, pp 5186-5192, issn 0008-5472Article