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Nature Genetics
|
November 1, 1993
Mitotic errors in trisomy 21
A Sensi, N Ricci
The New England Journal of Medicine
|
March 8, 1990
Mitochondrial DNA deletions and ophthalmoplegia
A Sensi, A Bonfatti
Studi Emigrazione : International Journal of Migration Studies
|
September 26, 2002
From the Alps to Atitlan: Italian emigration to Guatemala, 1870-1945
P A Sensi-isolani
The British Journal of Dermatology
|
June 1, 1986
Heritability of Behçet's disease
A Sensi, O R Baricordi
Clinical Genetics
|
November 1, 1990
Familial porencephaly
A Sensi, S Cerruti, E Calzolari, et al.
Clinical Genetics
|
September 1, 1987
Clinical anophthalmos in a family
A Sensi, C Incorvaia, A Sebastiani, et al.
American Journal of Medical Genetics
|
June 1, 1992
Familial atrial septal defect with prolonged atrioventricular conduction
G Bosi, A Sensi, E Calzolari, et al.
British Journal of Audiology
|
July 13, 2000
Clinical and radiological evaluation in children with microtia
F Calzolari, G Garani, A Sensi, et al.
Tissue Antigens
|
November 1, 1986
Hereditary hemorrhagic telangiectasy (HHT) and HLA
A Sensi, V Abbasciano, A Balboni, et al.
American Journal of Medical Genetics
|
April 1, 1994
Vohwinkel syndrome (mutilating keratoderma) associated with craniofacial anomalies
A Sensi, V Bettoli, M R Zampino, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 52) with videos related to
Sort By:
Page
of 6
Nature Genetics
|
November 1, 1993
Mitotic errors in trisomy 21
A Sensi, N Ricci
The New England Journal of Medicine
|
March 8, 1990
Mitochondrial DNA deletions and ophthalmoplegia
A Sensi, A Bonfatti
Studi Emigrazione : International Journal of Migration Studies
|
September 26, 2002
From the Alps to Atitlan: Italian emigration to Guatemala, 1870-1945
P A Sensi-isolani
The British Journal of Dermatology
|
June 1, 1986
Heritability of Behçet's disease
A Sensi, O R Baricordi
Clinical Genetics
|
November 1, 1990
Familial porencephaly
A Sensi, S Cerruti, E Calzolari, et al.
Clinical Genetics
|
September 1, 1987
Clinical anophthalmos in a family
A Sensi, C Incorvaia, A Sebastiani, et al.
American Journal of Medical Genetics
|
June 1, 1992
Familial atrial septal defect with prolonged atrioventricular conduction
G Bosi, A Sensi, E Calzolari, et al.
British Journal of Audiology
|
July 13, 2000
Clinical and radiological evaluation in children with microtia
F Calzolari, G Garani, A Sensi, et al.
Tissue Antigens
|
November 1, 1986
Hereditary hemorrhagic telangiectasy (HHT) and HLA
A Sensi, V Abbasciano, A Balboni, et al.
American Journal of Medical Genetics
|
April 1, 1994
Vohwinkel syndrome (mutilating keratoderma) associated with craniofacial anomalies
A Sensi, V Bettoli, M R Zampino, et al.
Page
of 6