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M Zollino

Showing results (1-10 of 67) with videos related to

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American Journal of Medical Genetics|October 16, 1996
More on the Noonan-CFC controversyG Neri, M Zollino
Acta Haematologica|January 1, 1987
Protective effect of S-adenosylmethionine against the induction of chromosome fragile sitesM Zollino, G Neri
European Journal of Human Genetics : EJHG|April 21, 2001
Genotype-phenotype correlations in Wolf-Hirschhorn syndromeM Zollino, G Neri
American Journal of Medical Genetics|December 5, 2000
Partial deletion of chromosome 12q is not usually associated with CFC syndromeM Zollino, G Neri
Cancer Genetics and Cytogenetics|October 15, 1990
Differential expression of FRA16B in peripheral lymphocytes and bone marrow cellsM Zollino, M Genuardi, G Neri
American Journal of Medical Genetics|December 2, 1996
From Pitt-Rogers-Danks syndrome to Wolf-Hirschhorn syndrome and back?M Zollino, R Bova, G Neri
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 29, 2001
[Diagnosis of Prader-Willi syndrome. Considerations on a case of erroneous diagnosis]S Scommegna, M Zollino, G Paolone
Clinical Genetics|February 6, 2013
Clinical and genetic heterogeneity of amyotrophic lateral sclerosisM Sabatelli, A Conte, M Zollino
Prenatal Diagnosis|April 24, 1999
Chromosome instability limited to the aneuploid clone in the Pallister-Killian syndrome: a pitfall in prenatal diagnosisM Zollino, J Bajer, G Neri
Journal of Medical Genetics|August 5, 2008
The terminal 760 kb region on 4p16 is unlikely to be the critical interval for growth delay in Wolf-Hirschhorn syndromeM Zollino, M Murdolo, G Neri
Pageof 7

Showing results (1-10 of 67) with videos related to

Sort By:
Pageof 7
American Journal of Medical Genetics|October 16, 1996
More on the Noonan-CFC controversyG Neri, M Zollino
Acta Haematologica|January 1, 1987
Protective effect of S-adenosylmethionine against the induction of chromosome fragile sitesM Zollino, G Neri
European Journal of Human Genetics : EJHG|April 21, 2001
Genotype-phenotype correlations in Wolf-Hirschhorn syndromeM Zollino, G Neri
American Journal of Medical Genetics|December 5, 2000
Partial deletion of chromosome 12q is not usually associated with CFC syndromeM Zollino, G Neri
Cancer Genetics and Cytogenetics|October 15, 1990
Differential expression of FRA16B in peripheral lymphocytes and bone marrow cellsM Zollino, M Genuardi, G Neri
American Journal of Medical Genetics|December 2, 1996
From Pitt-Rogers-Danks syndrome to Wolf-Hirschhorn syndrome and back?M Zollino, R Bova, G Neri
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 29, 2001
[Diagnosis of Prader-Willi syndrome. Considerations on a case of erroneous diagnosis]S Scommegna, M Zollino, G Paolone
Clinical Genetics|February 6, 2013
Clinical and genetic heterogeneity of amyotrophic lateral sclerosisM Sabatelli, A Conte, M Zollino
Prenatal Diagnosis|April 24, 1999
Chromosome instability limited to the aneuploid clone in the Pallister-Killian syndrome: a pitfall in prenatal diagnosisM Zollino, J Bajer, G Neri
Journal of Medical Genetics|August 5, 2008
The terminal 760 kb region on 4p16 is unlikely to be the critical interval for growth delay in Wolf-Hirschhorn syndromeM Zollino, M Murdolo, G Neri
Pageof 7