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Ringchromosom 18 bei einem Neugeborenen = Ring chromosome 18 in a newbornDÖTSCH, J; FÖRSTER, W; KÜHL, P. G et al.Monatsschrift für Kinderheilkunde. 1995, Vol 143, Num 5, pp 489-492, issn 0026-9298Article

A novel form of human polymorphism involving the hDHFR-ψ1 pseudogene identifies three RFLPsANAGNOU, N. P; ANTONARAKIS, S. E; O'BRIEN, S. J et al.Nucleic acids research. 1987, Vol 15, Num 13, issn 0305-1048, 5501Article

Intensive care in an adolescent with trisomy 18: an ethical dilemmaPIASTRA, Marco; CARESTA, Elena; CHIARETTI, Antonio et al.European journal of pediatrics. 2003, Vol 162, Num 11, pp 814-815, issn 0340-6199, 2 p.Article

Parental origin of the extra chromosome 18 in Edwards syndromeRAMESH, K. H; VERMA, R. S.Annales de génétique (Paris). 1996, Vol 39, Num 2, pp 110-112, issn 0003-3995Article

Follow-up of adult males with chromosome 18p deletionDE RAVEL, Thomy J. L; THIRY, Paul; FRYNS, Jean-Pierre et al.European journal of medical genetics. 2005, Vol 48, Num 2, pp 189-193, issn 1769-7212, 5 p.Article

Inversion, duplication, and changes in gene context are associated with human chromosome 18 evolutionDENNEHEY, Briana K; GUTCHES, Diane G; MCCONKEY, Edwin H et al.Genomics (San Diego, Calif.). 2004, Vol 83, Num 3, pp 493-501, issn 0888-7543, 9 p.Article

Assignment of the melanocortin 4 receptor (MC4R) gene to human chromosome band 18q22 by in situ hybridisation and radiation hybrid mappingSUNDARAMURTHY, D; CAMPBELL, D. A; LEEK, J. P et al.Cytogenetics and cell genetics. 1998, Vol 82, Num 1-2, pp 97-98, issn 0301-0171Conference Paper

Chromosome 18 aneuploidy-anatomical variations observed in cases of full and mosaic trisomy 18 and a case of deletion of the short arm of chromosome 18URBAN, B; BERSU, E. T.American journal of medical genetics. 1987, Vol 27, Num 2, pp 425-434, issn 0148-7299Article

Isolation of mapping of a polymorphic DNA sequence pEFZ10 on chromosome 18 [D18S22]KRAPCHO, K; NAKAMURA, Y; FUJIMOTO, E et al.Nucleic acids research. 1988, Vol 16, Num 3, issn 0305-1048, 1227Article

Denovo inherited 18p deletion in a mother-fetus pair with extremely variable expression, confirmed by fluorescence in situ hybridization (FISH) analysisTONK, V; KRISHNA, J.European journal of obstetrics, gynecology, and reproductive biology. 1997, Vol 73, Num 2, pp 193-196, issn 0301-2115Article

Maternal serum screening for fetal trisomy 18 : A comparison of fixed cutoff and patient-specific risk protocolsBENN, P. A; LEO, M. V; RODIS, J. F et al.Obstetrics and gynecology (New York. 1953). 1999, Vol 93, Num 5, pp 707-711, issn 0029-7844, 1Article

Hypothesis : association of the critical region of trisomy 18 and 18q2 : syndrome with dermatoglyphic findings and a growth suppressor (deleted in colon cancer) locusREED, T.Clinical genetics. 1991, Vol 39, Num 5, pp 391-395, issn 0009-9163Article

Inheritance of a Terminal 7.1 Mb 18p Deletion Flanked by a 2.3 Mb Duplication From a Physically Normal MotherMISCEO, Doriana; ØRSTAVIK, Karen Helene; LYBAEK, Helle et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 12, pp 2877-2881, issn 1552-4825, 5 p.Article

Autoimmune thyroiditis in 18Q deletion syndromeLOMENICK, Jefferson P; JACKSON SMITH, W; ROSE, Susan R et al.The Journal of pediatrics. 2005, Vol 147, Num 4, pp 541-543, issn 0022-3476, 3 p.Article

DNA sequence and analysis of human chromosome 18NUSBAUM, Chad; ZODY, Michael C; FITZGERALD, Michael G et al.Nature (London). 2005, Vol 437, Num 7058, pp 551-555, issn 0028-0836, 5 p.Article

Evidence for association of the myo-inositol monophosphatase 2 (IMPA2) gene with schizophrenia in Japanese samplesYOSHIKAWA, T; KIKUCHI, M; SHIMIZU, H et al.Molecular psychiatry. 2001, Vol 6, Num 2, pp 202-210, issn 1359-4184Article

A female with monosomy 18 mosaicism : a previously undescribed chromosome abnormalityKHALIFA, M. M; YAMASHIRO, H; DUNCAN, A. M. V et al.Clinical genetics. 1996, Vol 49, Num 6, pp 318-320, issn 0009-9163Article

Trisomy 18 : studies of the parent and cell division of origin and the effect of aberrant recombination on nondisjunctionFISHER, J. M; HARVEY, J. F; MORTON, N. E et al.American journal of human genetics. 1995, Vol 56, Num 3, pp 669-675, issn 0002-9297Article

Linkage analyses of chromosome 18 markers do not identify a major susceptibility locus for bipolar affective disorder in the old order amishPAULS, D. L; OTT, J; EGELAND, J. A et al.American journal of human genetics. 1995, Vol 57, Num 3, pp 636-643, issn 0002-9297Article

Survival in trisomy 18ROOT, S; CAREY, J. C.American journal of medical genetics. 1994, Vol 49, Num 2, pp 170-174, issn 0148-7299Article

Dinucleotide repeat polymorphism at the D18S365 locusABELS, S; ERDMANN, J; NÖTHEN, M. M et al.Human molecular genetics (Print). 1993, Vol 2, Num 10, issn 0964-6906, p. 1747Article

Low frequency mosaicism of normal cells in a 16-year-old girl with trisomy 18GREVE, G; WAALER, P. E; ROSENDAHL, K et al.Clinical genetics. 1993, Vol 43, Num 2, pp 83-87, issn 0009-9163Article

Molecular studies of trisomy 18FISHER, J. M; HARVEY, J. F; LINDENBAUM, R. H et al.American journal of human genetics. 1993, Vol 52, Num 6, pp 1139-1144, issn 0002-9297Article

Mapping the human melanocortin 2 receptor (adrenocorticotropic hormone receptor ; ACTHR) gene (MC2R) to the small arm of chromosome 18 (18p11.21-pter)VAMVAKOPOULOS, N. C; ROJAS, K; OVERHAUSER, J et al.Genomics (San Diego, Calif.). 1993, Vol 18, Num 2, pp 454-455, issn 0888-7543Article

Retrospective study of the parental origin of the extra chromosome in trisomy 18 (Edwards syndrome)NÖTHEN, M. M; EGGERMANN, T; ERDMANN, J et al.Human genetics. 1993, Vol 92, Num 4, pp 347-349, issn 0340-6717Article

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