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American Journal of Medical Genetics
|
October 16, 1996
More on the Noonan-CFC controversy
G Neri, M Zollino
Acta Haematologica
|
January 1, 1987
Protective effect of S-adenosylmethionine against the induction of chromosome fragile sites
M Zollino, G Neri
European Journal of Human Genetics : EJHG
|
April 21, 2001
Genotype-phenotype correlations in Wolf-Hirschhorn syndrome
M Zollino, G Neri
American Journal of Medical Genetics
|
December 5, 2000
Partial deletion of chromosome 12q is not usually associated with CFC syndrome
M Zollino, G Neri
Cancer Genetics and Cytogenetics
|
October 15, 1990
Differential expression of FRA16B in peripheral lymphocytes and bone marrow cells
M 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 sclerosis
M 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 diagnosis
M 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 syndrome
M Zollino, M Murdolo, G Neri
Page
of 7
Search research articles
Search
Showing results (1-10 of 67) with videos related to
Sort By:
Page
of 7
American Journal of Medical Genetics
|
October 16, 1996
More on the Noonan-CFC controversy
G Neri, M Zollino
Acta Haematologica
|
January 1, 1987
Protective effect of S-adenosylmethionine against the induction of chromosome fragile sites
M Zollino, G Neri
European Journal of Human Genetics : EJHG
|
April 21, 2001
Genotype-phenotype correlations in Wolf-Hirschhorn syndrome
M Zollino, G Neri
American Journal of Medical Genetics
|
December 5, 2000
Partial deletion of chromosome 12q is not usually associated with CFC syndrome
M Zollino, G Neri
Cancer Genetics and Cytogenetics
|
October 15, 1990
Differential expression of FRA16B in peripheral lymphocytes and bone marrow cells
M 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 sclerosis
M 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 diagnosis
M 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 syndrome
M Zollino, M Murdolo, G Neri
Page
of 7