American journal of human genetics

Label

• American journal of human genetics (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#rivistaDi

• Whole genome sequencing of 3,514 individuals from the isolated population of Sardinia (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
• DJ-1 gene in late-onset recessive Parkinsons disease. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
• Hallervorden Spatz syndrome (HSS) in two families from southern Italy : a clinical and genetic study . (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
• Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error (Articolo in rivista) (Prodotto della ricerca)
• The population structure and demographic history of Sardinia in relationship to neighboring populations. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
• Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia (Articolo in rivista) (Prodotto della ricerca)

Alternative label

• American journal of human genetics (literal)
• Am. j. hum. genet. (literal)
• AJHG (literal)

Language

• eng (literal)

Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#issn

• 1537-6605 (literal)

Preferred label

• American journal of human genetics (literal)

Publisher

• University of Chicago Press for the American Society of Human Genetics Chicago, Ill. : USA (literal)

Incoming links:

Rivista

• Hallervorden Spatz syndrome (HSS) in two families from southern Italy : a clinical and genetic study . (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
• DJ-1 gene in late-onset recessive Parkinsons disease. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
• Three novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus. (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)
• Nine Loci for Ocular Axial Length Identified through Genome-wide Association Studies, Including Shared Loci with Refractive Error (Articolo in rivista) (Prodotto della ricerca)
• Malfunction of nuclease ERCC1-XPF results in diverse clinical manifestations and causes Cockayne syndrome, xeroderma pigmentosum, and Fanconi anemia (Articolo in rivista) (Prodotto della ricerca)
• The population structure and demographic history of Sardinia in relationship to neighboring populations. (Abstract/Poster in convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1304)
• Whole genome sequencing of 3,514 individuals from the isolated population of Sardinia (Abstract/Poster in atti di convegno) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1302)