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Results: 1-12 |
Results: 12
GENERATION OF A TRANSCRIPTION MAP OF A 1 MBASE REGION CONTAINING THE HFE GENE (6P22)
Authors: TOTARO A ROETTO A ROMMENS JM GRIFA A CARELLA M DAGRUMA L VALENTINO MA DAMBROSIO L CICILANO M CAMASCHELLA C FRANCO B GASPARINI P
Citation: A. Totaro et al., GENERATION OF A TRANSCRIPTION MAP OF A 1 MBASE REGION CONTAINING THE HFE GENE (6P22), European journal of human genetics, 6(2), 1998, pp. 105-113
MOLECULAR-GENETICS OF OSTEOPOROSIS IN ITALY
Authors: DAGRUMA L BISCEGLIA L GASPARINI P ZELANTE L IOLASCON A IOLASCON G COLAPIETRO F FURLAN F BERTOLDO F
Citation: L. Dagruma et al., MOLECULAR-GENETICS OF OSTEOPOROSIS IN ITALY, European journal of human genetics, 6, 1998, pp. 4129-4129
MUTATION 35DELG IN THE CONNEXIN-26 GENE IS THE MAJOR CAUSE OF SPORADIC AND FAMILIAL CONGENITAL DEAFNESS IN MEDITERRANEAN PATIENTS
Authors: GASPARINI P FORTINA P SURREY S RABIONET R MELCHIONDA S DAGRUMA L RAPPAPORT E GOVEA N MILA MM ZELANTE L ESTIVILL X
Citation: P. Gasparini et al., MUTATION 35DELG IN THE CONNEXIN-26 GENE IS THE MAJOR CAUSE OF SPORADIC AND FAMILIAL CONGENITAL DEAFNESS IN MEDITERRANEAN PATIENTS, European journal of human genetics, 6, 1998, pp. 4200-4200
A NOVEL MUTATION IN THE MITOCHONDRIAL TRNA(VAL) GENE ASSOCIATED WITH A COMPLEX NEUROLOGICAL PRESENTATION
Authors: TIRANTI V DAGRUMA L PAREYSON D MORA M CARRARA F ZELANTE L GASPARINI P ZEVIANI M
Citation: V. Tiranti et al., A NOVEL MUTATION IN THE MITOCHONDRIAL TRNA(VAL) GENE ASSOCIATED WITH A COMPLEX NEUROLOGICAL PRESENTATION, Annals of neurology, 43(1), 1998, pp. 98-101
CONNEXIN-26 MUTATIONS IN SPORADIC AND INHERITED SENSORINEURAL DEAFNESS
Authors: ESTIVILL X FORTINA P SURREY S RABIONET R MELCHIONDA S DAGRUMA L MANSFIELD E RAPPAPORT E GOVEA N MILA M ZELANTE L GASPARINI P
Citation: X. Estivill et al., CONNEXIN-26 MUTATIONS IN SPORADIC AND INHERITED SENSORINEURAL DEAFNESS, Lancet, 351(9100), 1998, pp. 394-398
CONNEXIN26 MUTATIONS ASSOCIATED WITH THE MOST COMMON FORM OF NON-SYNDROMIC NEUROSENSORY AUTOSOMAL RECESSIVE DEAFNESS (DFNB1) IN MEDITERRANEANS
Authors: ZELANTE L GASPARINI P ESTIVILL X MELCHIONDA S DAGRUMA L GOVEA N MILA M DELLAMONICA M LUTFI J SHOHAT M MANSFIELD E DELGROSSO K RAPPAPORT E SURREY S FORTINA P
Citation: L. Zelante et al., CONNEXIN26 MUTATIONS ASSOCIATED WITH THE MOST COMMON FORM OF NON-SYNDROMIC NEUROSENSORY AUTOSOMAL RECESSIVE DEAFNESS (DFNB1) IN MEDITERRANEANS, Human molecular genetics, 6(9), 1997, pp. 1605-1609
A COMMON MUTATION IN THE CONNEXIN-26 GENE IS THE PRIMARY CAUSE OF SPORADIC AND FAMILIAR CONGENITAL DEAFNESS IN MEDITERRANEAN POPULATIONS
Authors: ESTIVILL X RABIONET K ZELANTE L MELCHIONDA S DAGRUMA L MILA M GOVEA N DELGROSSO K SURREY S MANSFIELD E RAPPAPORT E FORTINA P GASPARINI P
Citation: X. Estivill et al., A COMMON MUTATION IN THE CONNEXIN-26 GENE IS THE PRIMARY CAUSE OF SPORADIC AND FAMILIAR CONGENITAL DEAFNESS IN MEDITERRANEAN POPULATIONS, American journal of human genetics, 61(4), 1997, pp. 108-108
A NOVEL MUTATION IN THE MITOCHONDRIAL TRNA(VAL) GENE ASSOCIATED WITH A COMPLEX NEUROLOGICAL PRESENTATION
Authors: TIRANTI V CARRARA F DAGRUMA L PAREYSON D MORA M GASPARINI P ZEVIANI M
Citation: V. Tiranti et al., A NOVEL MUTATION IN THE MITOCHONDRIAL TRNA(VAL) GENE ASSOCIATED WITH A COMPLEX NEUROLOGICAL PRESENTATION, American journal of human genetics, 61(4), 1997, pp. 1882-1882
SCANNING THE FIRST PART OF THE NEUROFIBROMATOSIS TYPE-1 GENE BY RNA-SSCP - IDENTIFICATION OF 3 NOVEL MUTATIONS AND OF 2 NEW POLYMORPHISMS
Authors: GASPARINI P DAGRUMA L DECILLIS GP BALESTRAZZI P MINGARELLI R ZELANTE L
Citation: P. Gasparini et al., SCANNING THE FIRST PART OF THE NEUROFIBROMATOSIS TYPE-1 GENE BY RNA-SSCP - IDENTIFICATION OF 3 NOVEL MUTATIONS AND OF 2 NEW POLYMORPHISMS, Human genetics, 97(4), 1996, pp. 492-495
NEW POLYMORPHISMS AND MARKERS IN THE HLA CLASS-I REGION - RELEVANCE TO HEREDITARY HEMOCHROMATOSIS (HFE)
Authors: TOTARO A GRIFA A ROETTO A LUNARDI C DAGRUMA L SBAIZ L ZELANTE L DESANDRE G CAMASCHELLA C GASPARINI P
Citation: A. Totaro et al., NEW POLYMORPHISMS AND MARKERS IN THE HLA CLASS-I REGION - RELEVANCE TO HEREDITARY HEMOCHROMATOSIS (HFE), Human genetics, 95(4), 1995, pp. 429-434
PLASMID DNA AND LOW-FREQUENCY ELECTROMAGNETIC-FIELDS
Authors: DAGRUMA L COLOSIMO A ANGELONI U NOVELLI G DALLAPICCOLA B
Citation: L. Dagruma et al., PLASMID DNA AND LOW-FREQUENCY ELECTROMAGNETIC-FIELDS, Biomedicine & pharmacotherapy, 47(2-3), 1993, pp. 101-105
ISOLATION AND CLONING BY A POLYMERASE CHAIN-REACTION OF A GENOMIC DNAFRAGMENT OF THE HUMAN SLOW SKELETAL TROPONIN (TNNT1) GENE
Authors: NOVELLI G GENNARELLI M SANGIUOLO F DAGRUMA L LOCICERO S MELCHIONDA S DALLAPICCOLA B
Citation: G. Novelli et al., ISOLATION AND CLONING BY A POLYMERASE CHAIN-REACTION OF A GENOMIC DNAFRAGMENT OF THE HUMAN SLOW SKELETAL TROPONIN (TNNT1) GENE, Cell biochemistry and function, 11(3), 1993, pp. 187-191
Risultati: 1-12 |