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AJR. American Journal of Roentgenology
|
January 1, 1989
The blunt needle: a new percutaneous access device
E W Akins, I F Hawkins, C Mladinich, et al.
Human Genetics
|
March 1, 1996
A novel mechanism for the origin of supernumerary marker chromosomes
P Maraschio, R Tupler, E Rossi, et al.
Genetic Testing
|
April 29, 2005
Facioscapulohumeral muscular dystrophy type 1A in northwestern Tuscany: a molecular genetics-based epidemiological and genotype-phenotype study
R Sposìto, L Pasquali, F Galluzzi, et al.
Journal of Medical Genetics
|
March 1, 1997
A variant of the Nijmegen breakage syndrome with unusual cytogenetic features and intermediate cellular radiosensitivity
R Tupler, G L Marseglia, M Stefanini, et al.
Journal of Medical Genetics
|
May 1, 1996
Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy
R Tupler, A Berardinelli, L Barbierato, et al.
Journal of Medical Genetics
|
September 11, 1998
Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression
R Tupler, L Barbierato, M Memmi, et al.
Human Genetics
|
April 1, 1989
Regional assignment of the loci for adenylate kinase to 9q32 and for alpha 1-acid glycoprotein to 9q31-q32. A locus for Goltz syndrome in region 9q32-qter?
O Zuffardi, A Caiulo, P Maraschio, et al.
Human Genetics
|
March 1, 1996
An analysis of Xq deletions
P Maraschio, R Tupler, L Barbierato, et al.
American Journal of Human Genetics
|
December 11, 2002
A locus for migraine without aura maps on chromosome 14q21.2-q22.3
D Soragna, A Vettori, G Carraro, et al.
Human Molecular Genetics
|
May 1, 1993
A highly informative microsatellite repeat polymorphism in intron 1 of the human amyloid precursor protein (APP) gene
R Tupler, E Rogaeva, G Vaula, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 35) with videos related to
Sort By:
Page
of 4
AJR. American Journal of Roentgenology
|
January 1, 1989
The blunt needle: a new percutaneous access device
E W Akins, I F Hawkins, C Mladinich, et al.
Human Genetics
|
March 1, 1996
A novel mechanism for the origin of supernumerary marker chromosomes
P Maraschio, R Tupler, E Rossi, et al.
Genetic Testing
|
April 29, 2005
Facioscapulohumeral muscular dystrophy type 1A in northwestern Tuscany: a molecular genetics-based epidemiological and genotype-phenotype study
R Sposìto, L Pasquali, F Galluzzi, et al.
Journal of Medical Genetics
|
March 1, 1997
A variant of the Nijmegen breakage syndrome with unusual cytogenetic features and intermediate cellular radiosensitivity
R Tupler, G L Marseglia, M Stefanini, et al.
Journal of Medical Genetics
|
May 1, 1996
Monosomy of distal 4q does not cause facioscapulohumeral muscular dystrophy
R Tupler, A Berardinelli, L Barbierato, et al.
Journal of Medical Genetics
|
September 11, 1998
Identical de novo mutation at the D4F104S1 locus in monozygotic male twins affected by facioscapulohumeral muscular dystrophy (FSHD) with different clinical expression
R Tupler, L Barbierato, M Memmi, et al.
Human Genetics
|
April 1, 1989
Regional assignment of the loci for adenylate kinase to 9q32 and for alpha 1-acid glycoprotein to 9q31-q32. A locus for Goltz syndrome in region 9q32-qter?
O Zuffardi, A Caiulo, P Maraschio, et al.
Human Genetics
|
March 1, 1996
An analysis of Xq deletions
P Maraschio, R Tupler, L Barbierato, et al.
American Journal of Human Genetics
|
December 11, 2002
A locus for migraine without aura maps on chromosome 14q21.2-q22.3
D Soragna, A Vettori, G Carraro, et al.
Human Molecular Genetics
|
May 1, 1993
A highly informative microsatellite repeat polymorphism in intron 1 of the human amyloid precursor protein (APP) gene
R Tupler, E Rogaeva, G Vaula, et al.
Page
of 4