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M Fraccaro

Showing results (51-60 of 64) with videos related to

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Human Genetics|October 1, 1986
A 45,X male with a Yp/18 translocationE Maserati, F Waibel, B Weber, et al.
Human Genetics|January 1, 1983
Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainmentM Fraccaro, O Zuffardi, E Bühler, et al.
American Journal of Human Genetics|December 1, 1993
Homozygotes for the autosomal dominant neoplasia syndrome (MEN1)M L Brandi, G Weber, A Svensson, et al.
Journal of Medical Genetics|April 1, 1985
First trimester fetal diagnosis of genetic disorders: clinical evaluation of 250 casesB Brambati, G Simoni, C Danesino, et al.
Human Genetics|May 1, 1993
Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to YqB Bardoni, G Floridia, S Guioli, et al.
Human Genetics|January 1, 1982
Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 casesF Pasquali, P Bernasconi, R Casalone, et al.
Nature Genetics|August 1, 1994
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversalB Bardoni, E Zanaria, S Guioli, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeA Ballabio, B Bardoni, R Carrozzo, et al.
American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndromeC E Yu, J Oshima, K A Goddard, et al.
Human Genetics|January 1, 1983
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 familiesL Iselius, J Lindsten, A Aurias, et al.
Pageof 7

Showing results (51-60 of 64) with videos related to

Sort By:
Pageof 7
Human Genetics|October 1, 1986
A 45,X male with a Yp/18 translocationE Maserati, F Waibel, B Weber, et al.
Human Genetics|January 1, 1983
Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainmentM Fraccaro, O Zuffardi, E Bühler, et al.
American Journal of Human Genetics|December 1, 1993
Homozygotes for the autosomal dominant neoplasia syndrome (MEN1)M L Brandi, G Weber, A Svensson, et al.
Journal of Medical Genetics|April 1, 1985
First trimester fetal diagnosis of genetic disorders: clinical evaluation of 250 casesB Brambati, G Simoni, C Danesino, et al.
Human Genetics|May 1, 1993
Functional disomy of Xp22-pter in three males carrying a portion of Xp translocated to YqB Bardoni, G Floridia, S Guioli, et al.
Human Genetics|January 1, 1982
Pathogenetic significance of "pure" monosomy 7 in myeloproliferative disorders. Analysis of 14 casesF Pasquali, P Bernasconi, R Casalone, et al.
Nature Genetics|August 1, 1994
A dosage sensitive locus at chromosome Xp21 is involved in male to female sex reversalB Bardoni, E Zanaria, S Guioli, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 1, 1989
Contiguous gene syndromes due to deletions in the distal short arm of the human X chromosomeA Ballabio, B Bardoni, R Carrozzo, et al.
American Journal of Human Genetics|August 1, 1994
Linkage disequilibrium and haplotype studies of chromosome 8p 11.1-21.1 markers and Werner syndromeC E Yu, J Oshima, K A Goddard, et al.
Human Genetics|January 1, 1983
The 11q;22q translocation: a collaborative study of 20 new cases and analysis of 110 familiesL Iselius, J Lindsten, A Aurias, et al.
Pageof 7