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A Cama

Showing results (141-150 of 201) with videos related to

Pageof 21
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American Journal of Medical Genetics|December 5, 2000
Folate pathway gene alterations in patients with neural tube defectsP De Marco, A Moroni, E Merello, et al.
Cancer|December 1, 1996
Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis. Novel criteria of assessment and correlations with constitutional adenomatous polyposis coli gene mutationsR Valanzano, A Cama, R Volpe, et al.
Minerva Pediatrica|October 1, 1992
[Intracranial bacterial abscess and empyema]E Mantero, G Losurdo, S Carini, et al.
Human Mutation|January 1, 1995
Multiplex PCR analysis and genotype-phenotype correlations of frequent APC mutationsA Cama, R Palmirotta, M C Curia, et al.
Diabetes|April 1, 1992
Detection of mutations in insulin receptor gene by denaturing gradient gel electrophoresisF Barbetti, P V Gejman, S I Taylor, et al.
Human Mutation|January 1, 1994
A novel mutation at the splice junction of exon 9 of the APC gene in familial adenomatous polyposisA Cama, D L Esposito, R Palmirotta, et al.
British Journal of Cancer|January 15, 1999
Microsatellite instability in thyroid tumours and tumour-like lesionsD Lazzereschi, R Palmirotta, A Ranieri, et al.
Minerva Pediatrica|November 13, 2013
Glioneuronal tumors and epilepsy in children: seizure outcome related to lesionectomyA Consales, P Striano, P Nozza, et al.
European Review for Medical and Pharmacological Sciences|March 9, 2017
Comparative study between biodegradable nasopore (BNP) and Merocel hemox 10 cm after septo-turbinoplasty procedureA Romano, G Salzano, G Dell'Aversana Orabona, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|March 19, 2021
Human infection with an unknown species of Dracunculus in VietnamPham Ngoc Thach, H Rogier van Doorn, Henry S Bishop, et al.
Pageof 21

Showing results (141-150 of 201) with videos related to

Sort By:
Pageof 21
American Journal of Medical Genetics|December 5, 2000
Folate pathway gene alterations in patients with neural tube defectsP De Marco, A Moroni, E Merello, et al.
Cancer|December 1, 1996
Congenital hypertrophy of the retinal pigment epithelium in familial adenomatous polyposis. Novel criteria of assessment and correlations with constitutional adenomatous polyposis coli gene mutationsR Valanzano, A Cama, R Volpe, et al.
Minerva Pediatrica|October 1, 1992
[Intracranial bacterial abscess and empyema]E Mantero, G Losurdo, S Carini, et al.
Human Mutation|January 1, 1995
Multiplex PCR analysis and genotype-phenotype correlations of frequent APC mutationsA Cama, R Palmirotta, M C Curia, et al.
Diabetes|April 1, 1992
Detection of mutations in insulin receptor gene by denaturing gradient gel electrophoresisF Barbetti, P V Gejman, S I Taylor, et al.
Human Mutation|January 1, 1994
A novel mutation at the splice junction of exon 9 of the APC gene in familial adenomatous polyposisA Cama, D L Esposito, R Palmirotta, et al.
British Journal of Cancer|January 15, 1999
Microsatellite instability in thyroid tumours and tumour-like lesionsD Lazzereschi, R Palmirotta, A Ranieri, et al.
Minerva Pediatrica|November 13, 2013
Glioneuronal tumors and epilepsy in children: seizure outcome related to lesionectomyA Consales, P Striano, P Nozza, et al.
European Review for Medical and Pharmacological Sciences|March 9, 2017
Comparative study between biodegradable nasopore (BNP) and Merocel hemox 10 cm after septo-turbinoplasty procedureA Romano, G Salzano, G Dell'Aversana Orabona, et al.
International Journal of Infectious Diseases : IJID : Official Publication of the International Society for Infectious Diseases|March 19, 2021
Human infection with an unknown species of Dracunculus in VietnamPham Ngoc Thach, H Rogier van Doorn, Henry S Bishop, et al.
Pageof 21