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Results 1 to 25 of 1818

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Pleiotropic effects of a chromosome 3 locus on speech-sound disorder and readingSTEIN, Catherine M; SCHICK, James H; ELSTON, Robert C et al.American journal of human genetics. 2004, Vol 74, Num 2, pp 283-297, issn 0002-9297, 15 p.Article

Assignment of human filamin gene FLNB to human chromosome band 3p14.3 and identification of YACs containing the complete FLNB transcribed regionBRÖCKER, F; BARDENHEUER, W; VIETEN, L et al.Cytogenetics and cell genetics. 1999, Vol 85, Num 3-4, pp 267-268, issn 0301-0171Article

Induction of the common fragile site FRA3B does not affect FHIT expressionMICHAEL, Dagmar; RAJEWSKY, Manfred F.Oncogene (Basingstoke). 2001, Vol 20, Num 14, pp 1798-1801, issn 0950-9232Article

Mapping of the human ribosomal large subunit protein gene RPL29 to human chromosome 3q29-qterGARCIA-BARCELO, M; LAW, P. T. W; TSUI, S. K. W et al.Genomics (San Diego, Calif.). 1997, Vol 46, Num 1, pp 148-151, issn 0888-7543Article

Fine Mapping on Chromosome 10q22-q23 Implicates Neuregulin 3 in SchizophreniaCHEN, Pei-Lung; AVRAMOPOULOS, Dimitrios; WOLYNIEC, Paula et al.American journal of human genetics. 2009, Vol 84, Num 1, pp 21-34, issn 0002-9297, 14 p.Article

The DNA sequence, annotation and analysis of human chromosome 3MUZNY, Donna M; SCHERER, Steven E; DUGAN-ROCHA, Shannon et al.Nature (London). 2006, Vol 440, Num 7088, pp 1194-1198, issn 0028-0836, 5 p.Article

Human chromosome 3: integration of 60 NotI clones into a physical and gene mapSULIMOVA, G. E; KUTSENKO, A. S; BRAGA, E. A et al.Cytogenetic and genome research. 2002, Vol 98, Num 2-3, pp 177-183, issn 1424-8581, 7 p.Article

Assignment of the L32 ribosomal protein gene (RPL32) to human chromosome 3q13.3→q21 by in situ hybridizationVOROBIEVA, N. V; FILIPENKO, M. L; KARPOVA, G. G et al.Cytogenetics and cell genetics. 1997, Vol 77, Num 3-4, pp 190-191, issn 0301-0171Article

Radiation hybrid mapping of human arylacetamide deacetylase (AADAC) locus to chromosome 3YAMAZAKI, K; KUSANO, K; TADANO, K et al.Genomics (San Diego, Calif.). 1997, Vol 44, Num 2, pp 248-250, issn 0888-7543Article

Microarray Based Analysis of 3p25-p26 Deletions [3p- SyndromeSHUIB, Salwati; MCMULLAN, Dominic; MAHER, Eamonn R et al.American journal of medical genetics. Part A. 2009, Vol 149, Num 10, pp 2099-2105, issn 1552-4825, 7 p.Article

Functional characterization of the candidate tumor suppressor gene NPRL2/G21 located in 3p21.3cJINGFENG LI; FULI WANG; KASHUBA, Vladimir I et al.Cancer research (Baltimore). 2004, Vol 64, Num 18, pp 6438-6443, issn 0008-5472, 6 p.Article

Assignment of SHOX2 (alias OG12x and SHOT) to human chromosome bands 3q25→q26.1 by in situ hybridizationDE BAERE, E; SPELEMAN, F; VAN ROY, N et al.Cytogenetics and cell genetics. 1998, Vol 82, Num 3-4, pp 228-229, issn 0301-0171Article

Localization of human ERBA2 to the 3p22→3p24.1 region of chromosome 3 and variable deletion in small cell lung cancerDRABKIN, H; KAO, F.-T; HARTZ, J et al.Proceedings of the National Academy of Sciences of the United States of America. 1988, Vol 85, Num 23, pp 9258-9262, issn 0027-8424Article

The fragile site on chromosome 3SMEETS, D. F. C. M; SCHERES, J. M. J. C; HUSTINX, T. W. J et al.Human genetics. 1984, Vol 67, Num 3, issn 0340-6717, 351Article

The inducible fragile site on chromosome 3BERNAR, J; FUNDERBURK, S. J; SPARKES, R. S et al.Human genetics. 1984, Vol 66, Num 4, issn 0340-6717, 373Article

A new heritable fragile site on human chromosome 3MARKKANEN, A; KNUUTILA, S; DE LA CHAPELLE, A et al.Hereditas (Landskrona). 1983, Vol 99, Num 2, issn 0018-0661, 317Article

Two chimeric chromosomes of Streptomyces coelicolor A3(2) generated by single crossover of the wild-type chromosome and linear plasmid SCP1YAMASAKI, Masayuki; KINASHI, Haruyasu.Journal of bacteriology. 2004, Vol 186, Num 19, pp 6553-6559, issn 0021-9193, 7 p.Article

A refined comparative map between porcine chromosome 13 and human chromosome 3VAN POUCKE, M; YERLE, M; CHARDON, P et al.Cytogenetic and genome research. 2003, Vol 102, Num 1-4, pp 133-138, issn 1424-8581, 6 p.Article

A region on chromosome 3 is linked to dizygotic twinningBUSJAHN, Andreas; KNOBLAUCH, Hans; SCHUSTER, Herbert et al.Nature genetics. 2000, Vol 26, Num 4, pp 398-399, issn 1061-4036Article

Allele-specific late replication and fragility of the most active common fragile site, FRA3BLIANG WANG; DARLING, J; ZHANG, J.-S et al.Human molecular genetics (Print). 1999, Vol 8, Num 3, pp 431-437, issn 0964-6906Article

Assignmenta of FGF12, the human FGF homologous factor 1 gene, to chromosome 3q29→3qter by fluorescence in situ hybridizationLIU, Y; CHIU, I.-M.Cytogenetics and cell genetics. 1997, Vol 78, Num 1, pp 48-49, issn 0301-0171Article

Assignment of the gene for human tetranectin (TNA) to chromosome 3p22→p21.3 by somatic cell hybrid mappingDURKIN, M. E; NAYLOR, S. L; ALBRECHTSEN, R et al.Cytogenetics and cell genetics. 1997, Vol 76, Num 1-2, pp 39-40, issn 0301-0171Article

Chromosomal mapping of two novel human FGF genes, FGF11 and FGF12VERDIER, A.-S; MATTEI, M.-G; LOVEC, H et al.Genomics (San Diego, Calif.). 1997, Vol 40, Num 1, pp 151-154, issn 0888-7543Article

Linkage and cytogenetic mapping of a CAG repeat containing human cDNA to 3p24.2-p22POLYMEROPOULOS, M. H; IDE, S. E; BECKER, K et al.Cancer genetics and cytogenetics. 1996, Vol 92, Num 1, pp 46-49, issn 0165-4608Article

The human HCLS1 gene maps to chromosome 3q13 by fluorescence in situ hybridizationEGASHIRA, M; KITAMURA, D; WATANABE, T et al.Cytogenetics and cell genetics. 1996, Vol 72, Num 2-3, pp 175-176, issn 0301-0171Conference Paper

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