Search research articles
Contact Us
Filters
Showing results (1-10 of 17) with videos related to
Page
of 2
Sort By:
Human Mutation
|
January 1, 1994
Development of RNA-SSCP protocols for the identification and screening of CFTR mutations: identification of two new mutations
L Bisceglia, A Grifa, L Zelante, et al.
Annales De Genetique
|
June 24, 2003
Interstitial "de novo" tandem duplication of 7(q31.1-q35): first reported case
L Zelante, A I Croce, A Grifa, et al.
Molecular and Cellular Probes
|
October 1, 1993
Detection of a neurofibromatosis type I (NF1) homologous sequence by PCR: implications for the diagnosis and screening of genetic diseases
P Gasparini, A Grifa, P Origone, et al.
Human Genetics
|
November 1, 1994
A new complex polymorphic repeat close to the HLA-A and HLA-E loci
A Totaro, A Grifa, A Roetto, et al.
Molecular and Cellular Probes
|
June 1, 1995
Molecular screening of genetic defects with RNA-SSCP analysis: the PKU and cystinuria model
S Giannattasio, L Bisceglia, P Lattanzio, et al.
Human Genetics
|
December 1, 1994
The motilin gene: subregional localisation, tissue expression, DNA polymorphisms and exclusion as a candidate gene for the HLA-associated immotile cilia syndrome
P Gasparini, A Grifa, S Savasta, et al.
Biochemical and Biophysical Research Communications
|
October 1, 1998
GABA (gamma-amino-butyric acid) neurotransmission: identification and fine mapping of the human GABAB receptor gene
A Grifa, A Totaro, J M Rommens, et al.
Biochemical and Biophysical Research Communications
|
October 24, 1998
Cloning of a new gene (FB19) within HLA class I region
A Totaro, A Grifa, M Carella, et al.
Clinical Genetics
|
June 1, 1995
Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variant
A Grifa, M R Piemontese, S Melchionda, et al.
Human Mutation
|
December 19, 2001
Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment
N López-Bigas, S Melchionda, R de Cid, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 17) with videos related to
Sort By:
Page
of 2
Human Mutation
|
January 1, 1994
Development of RNA-SSCP protocols for the identification and screening of CFTR mutations: identification of two new mutations
L Bisceglia, A Grifa, L Zelante, et al.
Annales De Genetique
|
June 24, 2003
Interstitial "de novo" tandem duplication of 7(q31.1-q35): first reported case
L Zelante, A I Croce, A Grifa, et al.
Molecular and Cellular Probes
|
October 1, 1993
Detection of a neurofibromatosis type I (NF1) homologous sequence by PCR: implications for the diagnosis and screening of genetic diseases
P Gasparini, A Grifa, P Origone, et al.
Human Genetics
|
November 1, 1994
A new complex polymorphic repeat close to the HLA-A and HLA-E loci
A Totaro, A Grifa, A Roetto, et al.
Molecular and Cellular Probes
|
June 1, 1995
Molecular screening of genetic defects with RNA-SSCP analysis: the PKU and cystinuria model
S Giannattasio, L Bisceglia, P Lattanzio, et al.
Human Genetics
|
December 1, 1994
The motilin gene: subregional localisation, tissue expression, DNA polymorphisms and exclusion as a candidate gene for the HLA-associated immotile cilia syndrome
P Gasparini, A Grifa, S Savasta, et al.
Biochemical and Biophysical Research Communications
|
October 1, 1998
GABA (gamma-amino-butyric acid) neurotransmission: identification and fine mapping of the human GABAB receptor gene
A Grifa, A Totaro, J M Rommens, et al.
Biochemical and Biophysical Research Communications
|
October 24, 1998
Cloning of a new gene (FB19) within HLA class I region
A Totaro, A Grifa, M Carella, et al.
Clinical Genetics
|
June 1, 1995
Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variant
A Grifa, M R Piemontese, S Melchionda, et al.
Human Mutation
|
December 19, 2001
Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment
N López-Bigas, S Melchionda, R de Cid, et al.
Page
of 2