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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

CONTRIBUTION A L'ETUDE DU CHROMOSOME 18 EN ANNEAU (A PROPOS DE DEUX OBSERVATIONS).WALLERICH THEOBALD MF.1977; ; S.L.; DA. 1977; PP. 1-82; BIBL. 25 P.; (THESE DOCT. MED.; NANCY I)Thesis

A CASE OF RING 18 CHROMOSOME IN A SIBSHIP WITH MULTIPLE SPONTANEOUS ABORTIONSCOCO R; BARREIRO CZ; PENCHASZADEH VB et al.1975; ANN. GENET.; FR.; DA. 1975; VOL. 18; NO 2; PP. 135-137; ABS. FR.; BIBL. 3REF.Article

ANOMALIES CONSTITUTIONNELLES DU CHROMOSOME 18: MONOSOMIES PARTIELLES, ANNEAUX, TRISOMIE COMPLETE LIBRE. ETUDE DE CAS PERSONNELS ET REVUE DE LA LITTERATUREBRES MICHEL.1979; ; FRA; DA. 1979; 24; 88 P.: ILL.-PL.; 30 CM; BIBL. 61 REF.; TH.: MED./TOURS/1979Thesis

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

PARENTAL MOSAICISM IN TRISOMY 18 = MOSAICISME PARENTAL ET TRISOMIE 18BERATIS NG; KARDON NB; HSU LYF et al.1972; PEDIATRICS; U.S.A.; DA. 1972; VOL. 50; NO 6; PP. 908-911; BIBL. 22REF.Serial Issue

TRISOMY E (18) SYNDROME: CLINICAL SPECTRUM IN 12 NEW CASES, INCLUDING CHROMOSOME AUTORADIOGRAPHY IN 4 = SYNDROME DE TRISOMIE E (18): ANALYSE CLINIQUE DANS 12 NOUVEAUX CAS AVEC AUTORADIOGRAPHIE DES CHROMOSOMES DANS 4 CASWEBER FM; SPARKES RS.1970; J. MED. GENET.; G.B.; DA. 1970; VOL. 7; NO 4; PP. 363-366; BIBL. 14 REF.Serial Issue

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

Tissue-Limited Ring Chromosome 18 Mosaicism as a Cause of Pitt―Hopkins SyndromeTAKENOUCHI, Toshiki; YAGIHASHI, Tatsuhiko; TSUCHIYA, Hiroyuki et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 10, pp 2621-2623, issn 1552-4825, 3 p.Article

Tetrasomy 18p: Report of the Molecular and Clinical Findings of 43 IndividualsSEBOLD, Courtney; ROEDER, Elizabeth; O'DONNELL, Louise et al.American journal of medical genetics. Part A. 2010, Vol 152, Num 9, pp 2164-2172, issn 1552-4825, 9 p.Article

Structural analysis reflects the evolutionary relationship between the human desmocollin gene family membersCSERHALMI-FRIEDMAN, P. B; FRANK, J. A; AHMAD, W et al.Experimental dermatology. 2001, Vol 10, Num 2, pp 95-99, issn 0906-6705Article

Human mRNA capping enzyme (RNGTT) and cap methyltransferase (RNMT) map to 6q16 and 18p11.22-p11.23, respectivelyPILLUTLA, R. C; SHIMAMOTO, A; FURUICHI, Y et al.Genomics (San Diego, Calif.). 1998, Vol 54, Num 2, pp 351-353, issn 0888-7543Article

A human UPD-GalNAc : polypeptide, N-acetylgalactosaminyltranferase type 1 gene is located at the chromosomal region 18q12.1TAKAI, S; HINODA, Y; ADACHI, T et al.Human genetics. 1997, Vol 99, Num 3, pp 293-294, issn 0340-6717Article

A chromosome 18 genetic linkage study in three large Belgian pedigrees with bipolar disorderCLAES, S; RAEYMAEKERS, P; VAN BROECKHOVEN, C et al.Journal of affective disorders. 1997, Vol 43, Num 3, pp 195-205, issn 0165-0327Article

Psychiatric Syndromes in Individuals With Chromosome 18 AbnormalitiesZAVALA, Juan; RAMIREZ, Mercedes; MEDINA, Rolando et al.American journal of medical genetics. Part B, Neuropsychiatric genetics. 2010, Vol 153, Num 3, pp 837-845, issn 1552-4841, 9 p.Article

Trisomy 13/trisomy 18 mosaicism in an infantABE, K; HARADA, N; ITOH, T et al.Clinical genetics. 1996, Vol 50, Num 5, pp 300-303, issn 0009-9163Article

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