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A Sensi

Showing results (1-10 of 52) with videos related to

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

Showing results (1-10 of 52) with videos related to

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