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F Lo Curto

Showing results (21-30 of 31) with videos related to

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Annales De Genetique|January 1, 1984
A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosageP Maraschio, C Danesino, F Lo Curto, et al.
American Journal of Diseases of Children (1960)|July 1, 1974
XO and male phenotypeF Lo Curto, E Pucci, S Scappaticci, et al.
Prenatal Diagnosis|January 1, 1988
First trimester prenatal diagnosis of Sanfilippo disease (MPSIII) type BA Minelli, C Danesino, F Lo Curto, et al.
Clinical Genetics|November 1, 1986
A new chromosome instability disorderP Maraschio, D Peretti, S Lambiase, et al.
Human Genetics|January 1, 1982
Correlation between the number of sex chromosomes and the H-Y antigen titerM Fraccaro, A Mayerová, U Wolf, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1997
Insulin-like growth factors (IGF-I and IGF-II) and IGF-binding protein-3 production by fibroblasts of patients with Turner's syndrome in cultureA Barreca, D Larizza, G Damonte, et al.
Cancer Genetics and Cytogenetics|November 14, 1997
Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic lossL Seghezzi, C Dellavecchia, E Maserati, et al.
Cancer Genetics and Cytogenetics|February 15, 2001
Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator geneA Minelli, E Maserati, G Giudici, et al.
Leukemia|April 27, 2007
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCRG Porta, E Maserati, E Mattarucchi, et al.
Leukemia|January 17, 2009
The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndromeA Minelli, E Maserati, E Nicolis, et al.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Annales De Genetique|January 1, 1984
A liveborn 69,XXX triploid. Origin, X chromosome activity and gene dosageP Maraschio, C Danesino, F Lo Curto, et al.
American Journal of Diseases of Children (1960)|July 1, 1974
XO and male phenotypeF Lo Curto, E Pucci, S Scappaticci, et al.
Prenatal Diagnosis|January 1, 1988
First trimester prenatal diagnosis of Sanfilippo disease (MPSIII) type BA Minelli, C Danesino, F Lo Curto, et al.
Clinical Genetics|November 1, 1986
A new chromosome instability disorderP Maraschio, D Peretti, S Lambiase, et al.
Human Genetics|January 1, 1982
Correlation between the number of sex chromosomes and the H-Y antigen titerM Fraccaro, A Mayerová, U Wolf, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1997
Insulin-like growth factors (IGF-I and IGF-II) and IGF-binding protein-3 production by fibroblasts of patients with Turner's syndrome in cultureA Barreca, D Larizza, G Damonte, et al.
Cancer Genetics and Cytogenetics|November 14, 1997
Ph-positive CML in blastic phase with monosomy 7 in a Down syndrome patient. Monitoring by interphase cytogenetics and demonstration of maternal allelic lossL Seghezzi, C Dellavecchia, E Maserati, et al.
Cancer Genetics and Cytogenetics|February 15, 2001
Familial partial monosomy 7 and myelodysplasia: different parental origin of the monosomy 7 suggests action of a mutator geneA Minelli, E Maserati, G Giudici, et al.
Leukemia|April 27, 2007
Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCRG Porta, E Maserati, E Mattarucchi, et al.
Leukemia|January 17, 2009
The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndromeA Minelli, E Maserati, E Nicolis, et al.
Pageof 4