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G Gimelli

Showing results (21-30 of 64) with videos related to

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Human Genetics|March 1, 1993
Are the nail-patella syndrome and the autosomal Goltz-like syndrome the phenotypic expressions of different alleles at the COL5A1 locus?G M Ghiggeri, G Caridi, P Altieri, et al.
Gene|October 4, 2012
Molecular cytogenetic characterization of the first reported case of an inv dup (4p)(p15.1-pter) with a concomitant 4q35.1-qter deletion and normal parentsE Tassano, M G Alpigiani, P Salvati, et al.
Journal of Medical Genetics|May 23, 1998
Spectrum of clinical features associated with interstitial chromosome 22q11 deletionsM Di Rocco, A Buocompagni, P Picco, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Concomitant Turner syndrome and hemophilia A in a female with an idic(X)(p11) heterozygous at locus DXS52C Panarello, M Acquila, D Caprino, et al.
Clinical Genetics|January 1, 1996
The phenotype of a 45,X male with a Y/18 translocationG Gimelli, R Cinti, P Varone, et al.
Human Genetics|November 10, 2001
Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replicationK M Hassan, T Norwood, G Gimelli, et al.
Human Genetics|October 1, 1979
Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiencyL Tiepolo, P Maraschio, G Gimelli, et al.
Journal of Medical Genetics|February 7, 2001
Molecular characterisation of a supernumerary ring chromosome in a patient with VATER associationR Cinti, M Priolo, M Lerone, et al.
Human Genetics|August 1, 1993
Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instabilityA Pezzolo, G Gimelli, A Cohen, et al.
The Journal of Allergy and Clinical Immunology|August 10, 2001
T-cell apoptosis in ICF syndromeA Pezzolo, I Prigione, P Facchetti, et al.
Pageof 7

Showing results (21-30 of 64) with videos related to

Sort By:
Pageof 7
Human Genetics|March 1, 1993
Are the nail-patella syndrome and the autosomal Goltz-like syndrome the phenotypic expressions of different alleles at the COL5A1 locus?G M Ghiggeri, G Caridi, P Altieri, et al.
Gene|October 4, 2012
Molecular cytogenetic characterization of the first reported case of an inv dup (4p)(p15.1-pter) with a concomitant 4q35.1-qter deletion and normal parentsE Tassano, M G Alpigiani, P Salvati, et al.
Journal of Medical Genetics|May 23, 1998
Spectrum of clinical features associated with interstitial chromosome 22q11 deletionsM Di Rocco, A Buocompagni, P Picco, et al.
Cytogenetics and Cell Genetics|January 1, 1992
Concomitant Turner syndrome and hemophilia A in a female with an idic(X)(p11) heterozygous at locus DXS52C Panarello, M Acquila, D Caprino, et al.
Clinical Genetics|January 1, 1996
The phenotype of a 45,X male with a Y/18 translocationG Gimelli, R Cinti, P Varone, et al.
Human Genetics|November 10, 2001
Satellite 2 methylation patterns in normal and ICF syndrome cells and association of hypomethylation with advanced replicationK M Hassan, T Norwood, G Gimelli, et al.
Human Genetics|October 1, 1979
Multibranched chromosomes 1, 9, and 16 in a patient with combined IgA and IgE deficiencyL Tiepolo, P Maraschio, G Gimelli, et al.
Journal of Medical Genetics|February 7, 2001
Molecular characterisation of a supernumerary ring chromosome in a patient with VATER associationR Cinti, M Priolo, M Lerone, et al.
Human Genetics|August 1, 1993
Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instabilityA Pezzolo, G Gimelli, A Cohen, et al.
The Journal of Allergy and Clinical Immunology|August 10, 2001
T-cell apoptosis in ICF syndromeA Pezzolo, I Prigione, P Facchetti, et al.
Pageof 7