LIBORIO STUPPIA
- Type
- Persona (Classe)
- Label
- LIBORIO STUPPIA (literal)
- LIBORIO STUPPIA (literal)
- Subject
- Persona in rapporto
- Rapporto con CNR di LIBORIO STUPPIA (Rapporto con CNR)
- Autore CNR di
- Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA), (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification, (Articolo in rivista) (Prodotto della ricerca)
- Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis, (Articolo in rivista) (Prodotto della ricerca)
- Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene, (Articolo in rivista) (Prodotto della ricerca)
- Prevalence of chromosomal abnormalities in 2078 infertile couples referred for assisted reproductive techniques, (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- A novel mutation of the IRF6 gene in an italian family with Van der Woude symdrome, (Articolo in rivista) (Prodotto della ricerca)
- Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs, (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women, (Articolo in rivista) (Prodotto della ricerca)
- Microsatellite polymorphism of the human leptin gene (LEP) and risk of cardiovascular disease, (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Nome
- LIBORIO (literal)
- Cognome
- STUPPIA (literal)
- Afferisce a
Incoming links:
- Ha afferente
- Rapporto con persona
- Rapporto con CNR di LIBORIO STUPPIA (Rapporto con CNR)
- Autore CNR
- Prevalence of chromosomal abnormalities in 2078 infertile couples referred for assisted reproductive techniques, (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs, (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Folate gene polymorphisms and the risk of Down syndrome pregnancies in young Italian women, (Articolo in rivista) (Prodotto della ricerca)
- Microsatellite polymorphism of the human leptin gene (LEP) and risk of cardiovascular disease, (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA), (Articolo in rivista) (http://www.cnr.it/ontology/cnr/individuo/prodotto/TIPO1101)
- Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis, (Articolo in rivista) (Prodotto della ricerca)
- Spinal muscular atrophy genotyping by gene dosage using multiple ligation-dependent probe amplification, (Articolo in rivista) (Prodotto della ricerca)
- Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene, (Articolo in rivista) (Prodotto della ricerca)
- A novel mutation of the IRF6 gene in an italian family with Van der Woude symdrome, (Articolo in rivista) (Prodotto della ricerca)
- Http://www.w3.org/2004/02/skos/core#isSubjectOf
- Http://www.w3.org/2002/07/owl#sameAs
