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O Zuffardi

Showing results (81-90 of 159) with videos related to

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Cytogenetics and Cell Genetics|January 1, 1978
BSu restriction of DNA from cases exhibiting sex-chromosome abnormalitiesJ Kinross, M Fraccaro, S Scappaticci, et al.
American Journal of Medical Genetics|October 23, 1997
Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter-->q24::q21.32-->qter) and random X inactivationR Carrozzo, G Arrigo, E Rossi, et al.
Genomics|November 1, 1994
Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32C Gellera, E Verderio, G Floridia, et al.
Annales De Genetique|January 1, 1991
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detectionE Maserati, F Pasquali, O Zuffardi, et al.
Human Genetics|March 1, 1996
A novel mechanism for the origin of supernumerary marker chromosomesP Maraschio, R Tupler, E Rossi, et al.
Molecular Syndromology|July 26, 2013
De novo 15.5-Mb Interstitial Deletion in 5p in a Male Ascertained by OligospermiaI Papoulidis, A Vetro, K Kefalas, et al.
Current Medicinal Chemistry|June 12, 2012
The genetics of small-vessel diseaseA Bersano, S Debette, E R Zanier, et al.
Oncogene|December 22, 1999
Evidence for interaction between human PRUNE and nm23-H1 NDPKinaseA Reymond, S Volorio, G Merla, et al.
American Journal of Medical Genetics|November 1, 1991
Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiencyA Ballabio, M Zollo, R Carrozzo, et al.
Human Genetics|January 1, 1980
Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223L Tiepolo, O Zuffardi, M Fraccaro, et al.
Pageof 16

Showing results (81-90 of 159) with videos related to

Sort By:
Pageof 16
Cytogenetics and Cell Genetics|January 1, 1978
BSu restriction of DNA from cases exhibiting sex-chromosome abnormalitiesJ Kinross, M Fraccaro, S Scappaticci, et al.
American Journal of Medical Genetics|October 23, 1997
Multiple congenital anomalies, brain hypomyelination, and ocular albinism in a female with dup(X) (pter-->q24::q21.32-->qter) and random X inactivationR Carrozzo, G Arrigo, E Rossi, et al.
Genomics|November 1, 1994
Assignment of the human carnitine palmitoyltransferase II gene (CPT1) to chromosome 1p32C Gellera, E Verderio, G Floridia, et al.
Annales De Genetique|January 1, 1991
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detectionE Maserati, F Pasquali, O Zuffardi, et al.
Human Genetics|March 1, 1996
A novel mechanism for the origin of supernumerary marker chromosomesP Maraschio, R Tupler, E Rossi, et al.
Molecular Syndromology|July 26, 2013
De novo 15.5-Mb Interstitial Deletion in 5p in a Male Ascertained by OligospermiaI Papoulidis, A Vetro, K Kefalas, et al.
Current Medicinal Chemistry|June 12, 2012
The genetics of small-vessel diseaseA Bersano, S Debette, E R Zanier, et al.
Oncogene|December 22, 1999
Evidence for interaction between human PRUNE and nm23-H1 NDPKinaseA Reymond, S Volorio, G Merla, et al.
American Journal of Medical Genetics|November 1, 1991
Deletion of the distal short arm of the X chromosome (Xp) in a patient with short stature, chondrodysplasia punctata, and X-linked ichthyosis due to steroid sulfatase deficiencyA Ballabio, M Zollo, R Carrozzo, et al.
Human Genetics|January 1, 1980
Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223L Tiepolo, O Zuffardi, M Fraccaro, et al.
Pageof 16