http://www.cnr.it/ontology/cnr/individuo/editore/ID11299

University of Chicago Press

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University of Chicago Press (literal)
University of Chicago Press (literal)

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Elevated white blood cell counts associated with Ureaplasma urealyticum colonization in preterm neonates. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility. (Articolo in rivista) (Prodotto della ricerca)
Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: Site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severity (Articolo in rivista) (Prodotto della ricerca)
The regulation of social relationships (Contributo in volume (capitolo o saggio)) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1201)
Electron flux spectral imaging of solar flares through regularized analysis of hard X-ray source visibilities (Articolo in rivista) (Prodotto della ricerca)
Anisotropic bremsstrahlung emission and the form of regularized electron flux spectra in solar flares (Articolo in rivista) (Prodotto della ricerca)
Time constraints on the building of the Serre Batholith: Consequences for the thermal evolution of the Hercynian Continental Crust exposed in... (Articolo in rivista) (Prodotto della ricerca)
Pitfalls in homozygosity mapping. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
POF2 gene may be responsible for the ovarian phenotype of Turner syndrome. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
Combined Efforts till Death: Funerary Ritual and Social Statements in the Aegean Early Bronze Age (Contributo in volume (capitolo o saggio)) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1201)
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
Evaluation of algorithms for reconstructing electron spectra from their bremsstrahlung hard X-ray spectra (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency. (Articolo in rivista) (Prodotto della ricerca)
MOLECULAR AND CELLULAR ANALYSIS OF THE DNA-REPAIR DEFECT IN A PATIENT IN XERODERMA-PIGMENTOSUM COMPLEMENTATION GROUP-D WHO HAS THE CLINICAL-FEATURES OF XERODERMA-PIGMENTOSUM AND COCKAYNE-SYNDROME (Articolo in rivista) (Prodotto della ricerca)
Hard X-ray imaging of solar flares using interpolated visibilities (Articolo in rivista) (Prodotto della ricerca)
X;autosome balanced translocations and premature ovarian failure: chromatin organization around the breakpoints. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)

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University of Chicago Press, Chicago (USA) (literal)
University of Chicago Press, Chicago (USA) (literal)

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Evaluation of algorithms for reconstructing electron spectra from their bremsstrahlung hard X-ray spectra (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
Electron flux spectral imaging of solar flares through regularized analysis of hard X-ray source visibilities (Articolo in rivista) (Prodotto della ricerca)
X;autosome balanced translocations and premature ovarian failure: chromatin organization around the breakpoints. (Abstract/Poster in atti di convegno) (Prodotto della ricerca)
Combined Efforts till Death: Funerary Ritual and Social Statements in the Aegean Early Bronze Age (Contributo in volume (capitolo o saggio)) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1201)
Anisotropic bremsstrahlung emission and the form of regularized electron flux spectra in solar flares (Articolo in rivista) (Prodotto della ricerca)
Hard X-ray imaging of solar flares using interpolated visibilities (Articolo in rivista) (Prodotto della ricerca)
The regulation of social relationships (Contributo in volume (capitolo o saggio)) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1201)
Pitfalls in homozygosity mapping. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophy (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
Analysis of mutations in the XPD gene in Italian patients with trichothiodystrophy: Site of mutation correlates with repair deficiency, but gene dosage appears to determine clinical severity (Articolo in rivista) (Prodotto della ricerca)
A human homologue of the Drosophila melanogaster diaphanous gene is disrupted in a patient with premature ovarian failure: evidence for conserved function in oogenesis and implications for human sterility. (Articolo in rivista) (Prodotto della ricerca)
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathies. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
Elevated white blood cell counts associated with Ureaplasma urealyticum colonization in preterm neonates. (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency. (Articolo in rivista) (Prodotto della ricerca)
MOLECULAR AND CELLULAR ANALYSIS OF THE DNA-REPAIR DEFECT IN A PATIENT IN XERODERMA-PIGMENTOSUM COMPLEMENTATION GROUP-D WHO HAS THE CLINICAL-FEATURES OF XERODERMA-PIGMENTOSUM AND COCKAYNE-SYNDROME (Articolo in rivista) (Prodotto della ricerca)
POF2 gene may be responsible for the ovarian phenotype of Turner syndrome. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
Time constraints on the building of the Serre Batholith: Consequences for the thermal evolution of the Hercynian Continental Crust exposed in... (Articolo in rivista) (Prodotto della ricerca)

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