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au.\*:("FRENGEN, E")

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Long-range mapping of the calcium release channel and glucosephosphate isomerase loci using pulsed-field gel electrophoresisFRENGEN, E; DAVIES, W.Animal genetics (Print). 1995, Vol 26, Num 3, pp 181-184, issn 0268-9146Article

Isolation, characterization and chromosomal assignment of a partial cDNA for porcine 6-phosphogluconate dehydrogenaseHARBITZ, I; CHOWDHARY, B; CHOWDHARY, R et al.Hereditas (Landskrona). 1990, Vol 112, Num 1, pp 83-88, issn 0018-0661, 6 p.Article

A modular, positive selection bacterial artificial chromosome vector with multiple cloning sitesFRENGEN, E; WEICHENHAN, D; BAOHUI ZHAO et al.Genomics (San Diego, Calif.). 1999, Vol 58, Num 3, pp 250-253, issn 0888-7543Article

The gene cluster containing the LCAT gene is conserved between human and pigFRENGEN, E; THOMSEN, P. D; BREDE, G et al.Cytogenetics and cell genetics. 1997, Vol 76, Num 1-2, pp 53-57, issn 0301-0171Article

Physical linkage of the gene cluster containing the LCAT gene to the DNA marker D16S124 at human chromosome region 16q22.1FRENGEN, E; BREDE, G; LARSEN, F et al.Cytogenetics and cell genetics. 1995, Vol 68, Num 3-4, pp 194-196, issn 0301-0171Conference Paper

Assignment of the L11 ribosomal protein gene (RPL11) to human chromosome 1p36.1→p35 by in situ hybridizationGRAPHODATSKY, A. S; VOROBIEVA, N. V; FILIPENKO, M. L et al.Cytogenetics and cell genetics. 1999, Vol 84, Num 1-2, pp 97-98, issn 0301-0171Article

Structural and functional organization of the gene encoding the human thyrotropin-releasing hormone receptorMATRE, V; HØVRING, P. I; ØRSTAVIK, S et al.Journal of neurochemistry. 1999, Vol 72, Num 1, pp 40-50, issn 0022-3042Article

An improved approach for construction of bacterial artificial chromosome librariesOSOEGAWA, K; PENG YEONG WOON; BAOHUI ZHAO et al.Genomics (San Diego, Calif.). 1998, Vol 52, Num 1, pp 1-8, issn 0888-7543Article

A Translocation Between Xq21.33 and 22q13.33 Causes an Intragenic SHANK3 Deletion in a Woman With Phelan-McDermid Syndrome and Hypergonadotropic HypogonadismMISCEO, D; RØDNINGEN, O. K; BARØY, T et al.American journal of medical genetics. Part A. 2011, Vol 155, Num 2, pp 403-408, issn 1552-4825, 6 p.Article

SCA27 caused by a chromosome translocation: further delineation of the phenotypeMISCEO, D; FANNEMEL, M; BARØY, T et al.Neurogenetics (Oxford. Print). 2009, Vol 10, Num 4, pp 371-374, issn 1364-6745, 4 p.Article

Porcine SINEs : characterization and use in species-specific amplificationFRENGEN, E; THOMSEN, P; KRISTENSEN, T et al.Genomics (San Diego, Calif.). 1991, Vol 10, Num 4, pp 949-956, issn 0888-7543, 8 p.Article

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