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American Journal of Medical Genetics
|
August 1, 1991
Patient with multiple congenital anomalies and decreased production and processing of procollagen in cultured fibroblasts
L Pavone, G Incorpora, A Fiumara, et al.
Genomics
|
September 1, 1994
Localization of the human genes encoding the two subunits of general transcription factor TFIIE
M Purrello, C Di Pietro, A Rapisarda, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
September 1, 1995
[Recurrent facial paralysis in a child with renovascular hypertension]
P Smilari, C Incorpora, A Polizzi, et al.
American Journal of Medical Genetics
|
April 14, 1997
Another "new" form, the palagonia type of acrofacial dysostosis in a Sicilian family
G Sorge, L Pavone, A Polizzi, et al.
Neuropediatrics
|
April 1, 1992
Two brothers with a variant of hereditary sensory neuropathy
L Pavone, P Huttenlocher, L Siciliano, et al.
Minerva Stomatologica
|
March 1, 1991
[Juvenile osteomyelitis and osteopetrosis. A case report]
M A Battaglia, P Drigo, A M Laverda, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 1, 1993
Febrile and afebrile convulsions: a clinical follow-up
L Pavone, V Galli, R Rizzo, et al.
Medical Oncology (Northwood, London, England)
|
June 3, 2008
Natural killer cell cytotoxicity is enhanced by very low doses of rIL-2 and rIFN-alpha in patients with renal cell carcinoma
L Pavone, G Fanti, C Bongiovanni, et al.
Clinical Genetics
|
November 1, 1996
Routine clinical application of the FRAXA Pfu PCR assay: limits and utility
D F Condorelli, G Milana, P Dell'Albani, et al.
Journal of Medical Genetics
|
October 1, 1982
Hereditary twenty-nail dystrophy in a Sicilian family
L Pavone, S Li Volti, B Guarneri, et al.
Page
of 17
Search research articles
Search
Showing results (131-140 of 165) with videos related to
Sort By:
Page
of 17
American Journal of Medical Genetics
|
August 1, 1991
Patient with multiple congenital anomalies and decreased production and processing of procollagen in cultured fibroblasts
L Pavone, G Incorpora, A Fiumara, et al.
Genomics
|
September 1, 1994
Localization of the human genes encoding the two subunits of general transcription factor TFIIE
M Purrello, C Di Pietro, A Rapisarda, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
September 1, 1995
[Recurrent facial paralysis in a child with renovascular hypertension]
P Smilari, C Incorpora, A Polizzi, et al.
American Journal of Medical Genetics
|
April 14, 1997
Another "new" form, the palagonia type of acrofacial dysostosis in a Sicilian family
G Sorge, L Pavone, A Polizzi, et al.
Neuropediatrics
|
April 1, 1992
Two brothers with a variant of hereditary sensory neuropathy
L Pavone, P Huttenlocher, L Siciliano, et al.
Minerva Stomatologica
|
March 1, 1991
[Juvenile osteomyelitis and osteopetrosis. A case report]
M A Battaglia, P Drigo, A M Laverda, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
June 1, 1993
Febrile and afebrile convulsions: a clinical follow-up
L Pavone, V Galli, R Rizzo, et al.
Medical Oncology (Northwood, London, England)
|
June 3, 2008
Natural killer cell cytotoxicity is enhanced by very low doses of rIL-2 and rIFN-alpha in patients with renal cell carcinoma
L Pavone, G Fanti, C Bongiovanni, et al.
Clinical Genetics
|
November 1, 1996
Routine clinical application of the FRAXA Pfu PCR assay: limits and utility
D F Condorelli, G Milana, P Dell'Albani, et al.
Journal of Medical Genetics
|
October 1, 1982
Hereditary twenty-nail dystrophy in a Sicilian family
L Pavone, S Li Volti, B Guarneri, et al.
Page
of 17