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Identification of a new quantitative trait locus on equine chromosome 18 responsible for osteochondrosis in Hanoverian warmblood horsesLAMPE, V; DIERKS, C; KOMM, K et al.Journal of animal science. 2009, Vol 87, Num 11, pp 3477-3481, issn 0021-8812, 5 p.Article

The Kruppel-like zinc-finger gene ZNF236 is alternatively spliced and excluded as susceptibility gene for diabetic nephropathyHALAMA, Niels; YARD-BREEDIJK, Annette; VARDARLI, Irfan et al.Genomics (San Diego, Calif.). 2003, Vol 82, Num 3, pp 406-411, issn 0888-7543, 6 p.Article

Linkage and association of febrile seizures to the IMPA2 gene on human chromosome 18NAKAYAMA, J; YAMAMOTO, N; HAMANO, K et al.Neurology. 2004, Vol 63, Num 10, pp 1803-1807, issn 0028-3878, 5 p.Article

Trapping and sequence analysis of 1138 putative exons from human chromosome 18CHEN, H; WANG, N; MCLNNIS, M. G et al.Molecular psychiatry. 2003, Vol 8, Num 6, pp 619-623, issn 1359-4184, 5 p.Article

Ultrasonographic diagnosis of Trisomy 18 : Is it practical in the early second trimester?SHIELDS, L. E; CARPENTER, L. A; SMITH, K. M et al.Journal of ultrasound in medicine. 1998, Vol 17, Num 5, pp 327-331, issn 0278-4297Article

The gene encoding PBP74/CSA/motalin-1, a novel mouse hsp70, maps to mouse chromosome 18OHASHI, M; OYANAGI, M; HATAKEYAMA, K et al.Genomics (San Diego, Calif.). 1995, Vol 30, Num 2, pp 406-407, issn 0888-7543Article

Assignment of the metallothionein 2 gene (MT2A) to bovine chromosome 18 by somatic cell analysisRYAN, A. M; WOMACK, J. E.Animal genetics (Print). 1994, Vol 25, Num 3, issn 0268-9146, p. 196Article

The murine urea transporter genes Slc14a land Slc14a2 occur in tandem on chromosome 18FENTON, R. A; HEWITT, J. E; HOWORTH, A et al.Cytogenetics and cell genetics. 1999, Vol 87, Num 1-2, pp 95-96, issn 0301-0171Article

Locus-specific dual color-probe for the enumeration of chromosome 18 in rapid FISH aneuploidy testing on uncultured amniocytesSOUCY, Jean-François; LAVOIE, Josée; DUNCAN, Alessandra M. V et al.Prenatal diagnosis. 2010, Vol 30, Num 8, pp 811-812, issn 0197-3851, 2 p.Article

Stabilization of a terminal inversion duplication of 8p by telomere capture from 18qKOSTINER, D. R; NGUYEN, H; COX, V. A et al.Cytogenetic and genome research. 2002, Vol 98, Num 1, pp 9-12, issn 1424-8581, 4 p.Article

Evaluation of the ovine Callipyge locus : I. relative chromosomal position and gene actionFREKING, B. A; KEELE, J. W; BEATTIE, C. W et al.Journal of animal science. 1998, Vol 76, Num 8, pp 2062-2071, issn 0021-8812Article

Pericentric inversion of chromosome 18 in parents leading to a phenotypically normal child with segmental uniparental disomy 18KARIMINEJAD, Ariana; KARIMINEJAD, Roxana; MOSHTAGH, Azadeh et al.European journal of human genetics. 2011, Vol 19, Num 5, pp 555-560, issn 1018-4813, 6 p.Article

DYT7 Gene Locus for Cervical Dystonia on Chromosome 18p Is QuestionableWINTER, Pia; KAMM, Christoph; BISKUP, Saskia et al.Movement disorders. 2012, Vol 27, Num 14, pp 1819-1821, issn 0885-3185, 3 p.Article

Familial high myopia linkage to chromosome 18pLAM, Dennis S. C; TAM, Pancy O. S; FAN, Dorothy S. P et al.Ophthalmologica (Basel). 2003, Vol 217, Num 2, pp 115-118, issn 0030-3755, 4 p.Article

Familial 18 centromere variant resulting in difficulties in interpreting prenatal interphase FISHBOURTHOUMIEU, S; ESCLAIRE, F; TERRO, F et al.Morphologie. 2010, Vol 94, Num 306, pp 68-72, issn 1286-0115, 5 p.Article

Refined positioning of a quantitative trait locus affecting somatic cell score on chromosome 18 in the German Holstein using linkage disequilibriumBAES, C; BRAND, B; MAYER, M et al.Journal of dairy science. 2009, Vol 92, Num 8, pp 4048-4056, issn 0022-0302, 9 p.Article

A major locus on mouse chromosome 18 controls XX sex reversal in Odd sex (Ods) miceYANGJUN QIN; POIRIER, Christophe; TRUONG, Cavatina et al.Human molecular genetics (Print). 2003, Vol 12, Num 5, pp 509-515, issn 0964-6906, 7 p.Article

Anaesthetic management for Edward's syndromeCOURREGES, P; NIEUVIARTS, R; LECOUTRE, D et al.Paediatric anaesthesia (Paris). 2003, Vol 13, Num 3, pp 267-269, issn 1155-5645, 3 p.Article

The SSX gene family: Characterization of 9 complete genesGÜRE, Ali O; WEI, Isaac J; OLD, Lloyd J et al.International journal of cancer. 2002, Vol 101, Num 5, pp 448-453, issn 0020-7136, 6 p.Article

Suggestive evidence for association of human chromosome 18q12-q21 and its orthologue on rat and mouse chromosome 18 with several autoimmune diseasesMERRIMAN, Tony R; CORDELL, Heather J; WORDSWORTH, Paul et al.Diabetes (New York, NY). 2001, Vol 50, Num 1, pp 184-194, issn 0012-1797Article

Hearing impairment in 18q deletion syndromeJAYARAJAN, V; SWAN, I. R. C; PATTON, M. A et al.Journal of laryngology and otology. 2000, Vol 114, Num 12, pp 963-966, issn 0022-2151Article

Assignment¹ of the histone deacetylase gene (Hdac3) to mouse chromosome 18B3 by in situ hybridizationMAHLKNECHT, U; BUCALA, R; VERDIN, E et al.Cytogenetics and cell genetics. 1999, Vol 84, Num 3-4, pp 192-193, issn 0301-0171Article

High-resolution gametic map of the sheep callipyge region : linkage heterogeneity among rams detected by sperm typing amongLIEN, S; COCKETT, N. E; KLUNGLAND, H et al.Animal genetics (Print). 1999, Vol 30, Num 1, pp 42-46, issn 0268-9146Article

Sporadic focal dystonia in Northwest Germany : Molecular basis on chromosome 18pLEUBE, B; HENDGEN, T; KESSLER, K. R et al.Annals of neurology. 1997, Vol 42, Num 1, pp 111-114, issn 0364-5134Article