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A Rasore Quartino

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La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1993
[Syndromes from birth to adulthood]A Rasore-Quartino
Acta Geneticae Medicae Et Gemellologiae|January 1, 1977
Type A2 brachydactily: report of a new familyA Rasore-Quartino, G Camera
Pathologica|May 1, 1993
[Pharmacokinetics of cytochrome P-450]A Rasore-Quartino, G Frenquellucci
Pathologica|March 1, 1993
[Spondylo-epiphyseal dysplasia tarda with progressive arthropathy: description of a patient whose mother showed minimal features of the disease]A Rasore-Quartino, A Camera, G Camera
Human Genetics|October 1, 1989
Expression of the human ETS-2 oncogene in normal fetal tissues and in the brain of a fetus with trisomy 21M Baffico, L Perroni, A Rasore-Quartino, et al.
La Ricerca in Clinica E in Laboratorio|April 1, 1983
A case of congenital afibrinogenemia. Study of a new familyA Galletti, E Barone, G Gastaldi, et al.
Pediatric Hematology and Oncology|April 1, 1993
Dyskeratosis congenita: unusual presenting features within a kindredG L Forni, C Melevendi, S Jappelli, et al.
Scandinavian Journal of Haematology|May 1, 1978
Coexistence of haemophilia A and von Willebrand's disease in the same kindredG Gastaldi, A Rasore-Quartino, A Galletti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[Yersinia enterocolitica sepsis in splenectomized thalassemic subjects. Description of 2 cases]A Rasore-Quartino, A Mattiello, M Cominetti, et al.
Journal of Medical Genetics|January 11, 2000
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)W Wuyts, E Cleiren, T Homfray, et al.
Pageof 2

Showing results (1-10 of 18) with videos related to

Sort By:
Pageof 2
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|May 1, 1993
[Syndromes from birth to adulthood]A Rasore-Quartino
Acta Geneticae Medicae Et Gemellologiae|January 1, 1977
Type A2 brachydactily: report of a new familyA Rasore-Quartino, G Camera
Pathologica|May 1, 1993
[Pharmacokinetics of cytochrome P-450]A Rasore-Quartino, G Frenquellucci
Pathologica|March 1, 1993
[Spondylo-epiphyseal dysplasia tarda with progressive arthropathy: description of a patient whose mother showed minimal features of the disease]A Rasore-Quartino, A Camera, G Camera
Human Genetics|October 1, 1989
Expression of the human ETS-2 oncogene in normal fetal tissues and in the brain of a fetus with trisomy 21M Baffico, L Perroni, A Rasore-Quartino, et al.
La Ricerca in Clinica E in Laboratorio|April 1, 1983
A case of congenital afibrinogenemia. Study of a new familyA Galletti, E Barone, G Gastaldi, et al.
Pediatric Hematology and Oncology|April 1, 1993
Dyskeratosis congenita: unusual presenting features within a kindredG L Forni, C Melevendi, S Jappelli, et al.
Scandinavian Journal of Haematology|May 1, 1978
Coexistence of haemophilia A and von Willebrand's disease in the same kindredG Gastaldi, A Rasore-Quartino, A Galletti, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[Yersinia enterocolitica sepsis in splenectomized thalassemic subjects. Description of 2 cases]A Rasore-Quartino, A Mattiello, M Cominetti, et al.
Journal of Medical Genetics|January 11, 2000
The ALX4 homeobox gene is mutated in patients with ossification defects of the skull (foramina parietalia permagna, OMIM 168500)W Wuyts, E Cleiren, T Homfray, et al.
Pageof 2