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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

46,XY,18q+ /46,XY,18q- mosaicism in a fragile X prenatal diagnosisRODRIGUEZ-REVENGA, Laia; BADENAS, Celia; MADRIGAL, Irene et al.Prenatal diagnosis. 2005, Vol 25, Num 6, pp 448-450, issn 0197-3851, 3 p.Article

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

Système de groupe sanguin Kidd. Structure et fonction du transporteur d'urée du globule rouge et hétérogénéité moléculaire du phénotype Jk_null = Kidd blood group system. Structure and function of the red cell urea transporter and molecular heterogeneity of the Jk_null phenotypeSidoux Walter, Frederic; Cartron, Jean-Pierre.2000, 235 p.Thesis

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

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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

Maspin: the most commonly-expressed gene of the 18q21.3 serpin cluster in lung cancer: is strongly expressed in preneoplastic bronchial lesionsSMITH, Shirley L; WATSON, Suzanne G; RATSCHILLER, Daniel et al.Oncogene (Basingstoke). 2003, Vol 22, Num 54, pp 8677-8687, issn 0950-9232, 11 p.Article

Linkage of essential hypertension to chromosome 18qKRISTJANSSON, Kristleifur; MANOLESCU, Andrei; STEFANSSON, Kari et al.Hypertension (Dallas, Tex. 1979). 2002, Vol 39, Num 6, pp 1044-1049, issn 0194-911XArticle

Balding: a new mutation on mouse chromosome 18 causing hair loss and immunological defectsDAVISSON, M. T; COOK, S. A; JOHNSON, K. R et al.The journal of heredity. 1994, Vol 85, Num 2, pp 134-136, issn 0022-1503Article

S0306 ― a molecular marker at pig chromosome 18q24THOMSEN, P. D; HØYHEIM, B.Animal genetics (Print). 1994, Vol 25, Num 5, issn 0268-9146, p. 377Article

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

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Down-regulated expression of SERPIN genes located on chromosome 18q21 in oral squamous cell carcinomasSHIIBA, Masashi; NOMURA, Hitomi; UZAWA, Katsuhiro et al.Oncology reports. 2010, Vol 24, Num 1, pp 241-249, issn 1021-335X, 9 p.Article

Congenital aural atresia in 18q deletion or de Grouchy syndromeNUIJTEN, Inge; ADMIRAAL, Ronald; VAN BUGGENHOUT, Griet et al.Otology & neurotology. 2003, Vol 24, Num 6, pp 900-906, issn 1531-7129, 7 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 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

Maternal serum cell-free fetal DNA levels are increased in cases of trisomy 13 but not trisomy 18WATAGANARA, Tuangsit; LESHANE, Erik S; FARINA, Antonio et al.Human genetics. 2003, Vol 112, Num 2, pp 204-208, issn 0340-6717, 5 p.Article