Skip to Main Content (Press Enter)
×
Home
Persone
Pubblicazioni
Strutture
Competenze
IT
EN
☰
UNI-FIND
|
UNI-FIND
cnr.it
IT
EN
×
Home
Persone
Pubblicazioni
Strutture
Competenze
☰
Pubblicazioni
JOURNAL OF HUMAN GENETICS
Rivista
Codice:
E092133
ISSN:
1434-5161
Dati Generali
Dati Generali
Pubblicazioni (5)
A locus for familial skewed X chromosome inactivation maps to chromosome Xq25 in a family with a female manifesting Lowe syndrome.
Articolo
A novel founder MYO15A frameshift duplication is the major cause of genetic hearing loss in Oman
Articolo
A shared haplotype for dentatorubropallidoluysian atrophy (DRPLA) in Italian families testifies of the recent introduction of the mutation
Articolo
A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype
Articolo
Genetic affinity and admixture of northern Thai people along their migration route in northern Thailand: Evidence from autosomal STR loci
Articolo
No Results Found
