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Pubblicazioni
GENOMICS
Rivista
Codice:
E069825
ISSN:
0888-7543
Dati Generali
Dati Generali
Pubblicazioni (20)
Pulisci
Ordina Pubblicazioni:
ascendente
decrescente
Assignment of X-linked hydrocephalus to Xq28 by linkage analysis
Articolo
Characterization of Cxorf5 (71-7A), a novel human cDNA mapping to Xp22 and encoding a protein containing coiled-coil alpha-helical domains
Articolo
Construction of a YAC contig covering human chromosome 6p22
Articolo
Fine mapping and cloning of the breakpoint associated with Menkes syndrome in a female patient
Articolo
Fra, A.M., Mastroianni, N., Mancini, M., Pasqualetto, E., Sitia, R., Human caveolin-1 and caveolin-2 are closely linked genes colocalized with WI-5336 in a region of 7q31 frequently deleted in tumors
Articolo
Genetic refinement and physical mapping of the CMT4B gene on chromosome 11q22
Articolo
Hereditary Hemochromatosis: generation of a transcription map within a refined and extended map of HLA class I region
Articolo
Hmg4, a new member of the Hmg1/2 gene family
Articolo
Identification and characterization of AFG3L2, a novel paraplegin-related gene
Articolo
Identification and characterization of CDS2, a mammalian homolog of the Drosophila CDP-diacylglycerol synthase gene
Articolo
Identification and characterization of YME1L1, a novel paraplegin-related gene
Articolo
Identification and characterization of a novel serine-threonine kinase gene from the Xp22 region
Articolo
Isolation and characterization of a highly polymorphic human locus (DXS455) in proximal Xq28
Articolo
KIF3C, a novel member of the kinesin superfamily: sequence, expression, and mapping to human chromosome 2 at 2p23
Articolo
MINCR: A long non-coding RNA shared between cancer and neurodegeneration
Articolo
Molecular cloning, expression pattern, and chromosomal localization of the human Na-Cl thiazide-sensitive cotransporter (SLC12A3)
Articolo
PKNOX1, a gene encoding PREP1, a new regulator of Pbx activity, maps on human chromosome 21q22.3 and murine chromosome 17B/C
Articolo
Simultaneous screening for beta-thalassemia mutations by chemical cleavage of mismatch
Articolo
The active gene that encodes human high mobility group 1 protein (HMG1) contains introns and maps to chromosome 13
Articolo
cDNA sequence, map, and expression of the murine homolog of GTBP, a DNA mismatch repair gene
Articolo
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