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Journal of Medical Genetics
|
May 1, 1996
Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD)
G Deidda, S Cacurri, N Piazzo, et al.
Haematologica
|
September 1, 1996
Detection of alpha-globin gene disorders by a simple PCR methodology
E Foglietta, G Deidda, B Graziani, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1995
Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter
G Deidda, S Cacurri, P Grisanti, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica
|
December 1, 1996
[Developments in the last 10 years in diagnostic imaging discovery of renal carcinoma]
G Deidda, A Paoni, A Pischedda, et al.
British Journal of Haematology
|
September 1, 1991
A new beta-thalassaemia frameshift mutation detected by PCR after selective hybridization to immobilized oligonucleotides
G Deidda, A Novelletto, M Hafez, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica
|
August 1, 1993
[The role of echography in the intraoperative study of non-palpable testicular masses]
C Trombetta, M Deriu, E Salisci, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica
|
September 1, 1994
[Urologic applications of intralaparoscopic echography]
C Trombetta, M Deriu, E Salisci, et al.
Human Mutation
|
January 1, 1995
Analysis of beta-thalassemia mutations in the United Arab Emirates provides evidence for recurrent origin of the IVSI nt 5 (G-C) mutation
R De Leo, G Deidda, A Novelletto, et al.
Hemoglobin
|
January 1, 1990
A new beta-thalassemia mutation produced by a single nucleotide substitution in the conserved dinucleotide sequence of the IVS-I consensus acceptor site (AG----AA)
G Deidda, A Novelletto, M Hafez, et al.
American Journal of Human Genetics
|
June 23, 1998
Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy
S Cacurri, N Piazzo, G Deidda, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 24) with videos related to
Sort By:
Page
of 3
Journal of Medical Genetics
|
May 1, 1996
Direct detection of 4q35 rearrangements implicated in facioscapulohumeral muscular dystrophy (FSHD)
G Deidda, S Cacurri, N Piazzo, et al.
Haematologica
|
September 1, 1996
Detection of alpha-globin gene disorders by a simple PCR methodology
E Foglietta, G Deidda, B Graziani, et al.
European Journal of Human Genetics : EJHG
|
January 1, 1995
Physical mapping evidence for a duplicated region on chromosome 10qter showing high homology with the facioscapulohumeral muscular dystrophy locus on chromosome 4qter
G Deidda, S Cacurri, P Grisanti, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica
|
December 1, 1996
[Developments in the last 10 years in diagnostic imaging discovery of renal carcinoma]
G Deidda, A Paoni, A Pischedda, et al.
British Journal of Haematology
|
September 1, 1991
A new beta-thalassaemia frameshift mutation detected by PCR after selective hybridization to immobilized oligonucleotides
G Deidda, A Novelletto, M Hafez, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica
|
August 1, 1993
[The role of echography in the intraoperative study of non-palpable testicular masses]
C Trombetta, M Deriu, E Salisci, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica
|
September 1, 1994
[Urologic applications of intralaparoscopic echography]
C Trombetta, M Deriu, E Salisci, et al.
Human Mutation
|
January 1, 1995
Analysis of beta-thalassemia mutations in the United Arab Emirates provides evidence for recurrent origin of the IVSI nt 5 (G-C) mutation
R De Leo, G Deidda, A Novelletto, et al.
Hemoglobin
|
January 1, 1990
A new beta-thalassemia mutation produced by a single nucleotide substitution in the conserved dinucleotide sequence of the IVS-I consensus acceptor site (AG----AA)
G Deidda, A Novelletto, M Hafez, et al.
American Journal of Human Genetics
|
June 23, 1998
Sequence homology between 4qter and 10qter loci facilitates the instability of subtelomeric KpnI repeat units implicated in facioscapulohumeral muscular dystrophy
S Cacurri, N Piazzo, G Deidda, et al.
Page
of 3