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American Journal of Medical Genetics
|
October 1, 1989
Dermatoglyphics in von Recklinghausen neurofibromatosis
R Pallotta, G Carlone, A Petrucci, et al.
Annales De Genetique
|
January 1, 1996
Further delineation of 7p trisomy. Case report and review of literature
R Pallotta, L Dalprà, P Fusilli, et al.
American Journal of Medical Genetics
|
December 26, 2001
A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency
R Pallotta, L Dalprà, M Miozzo, et al.
American Journal of Medical Genetics
|
March 21, 1998
Confirmation of the colobomatous macrophthalmia with microcornea syndrome: report of another family
R Pallotta, P Fusilli, G Sabatino, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 27, 1998
Hypoglycemia in childhood: a clinical approach
A Verrotti, P Fusilli, R Pallotta, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
November 1, 1983
[Pharmacological prevention of exercise-induced bronchospasm: review of the literature and trial of disodium cromoglycate, fenoterol and ipratropium bromide in a pediatric population]
M Verini, F Chiarelli, A Di Tullio, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1984
[Evaluation of the metacarpophalangeal profile (MPP) and of the dermatoglyphic pattern in Crouzon's syndrome]
R Pallotta, R Nardi, E Del Vomano, et al.
Acta Stomatologica Belgica
|
June 1, 1989
Enamel defects in a case of Menkes' syndrome
R Pallotta, F Del Rosso, S Domizio, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1984
[Long-term effects of neonatal medium-degree hyperbilirubinemia on brainstem evoked potentials]
R Pallotta, M Minervino, G Sabatino, et al.
Clinical Genetics
|
November 1, 1996
Cerebral defects confirm midline developmental field disturbances in supernumerary der(22), t(11;22) syndrome
R Pallotta, P Fusilli, T Ehresmann, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
American Journal of Medical Genetics
|
October 1, 1989
Dermatoglyphics in von Recklinghausen neurofibromatosis
R Pallotta, G Carlone, A Petrucci, et al.
Annales De Genetique
|
January 1, 1996
Further delineation of 7p trisomy. Case report and review of literature
R Pallotta, L Dalprà, P Fusilli, et al.
American Journal of Medical Genetics
|
December 26, 2001
A patient defines the interstitial 1q deletion syndrome characterized by antithrombin III deficiency
R Pallotta, L Dalprà, M Miozzo, et al.
American Journal of Medical Genetics
|
March 21, 1998
Confirmation of the colobomatous macrophthalmia with microcornea syndrome: report of another family
R Pallotta, P Fusilli, G Sabatino, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
June 27, 1998
Hypoglycemia in childhood: a clinical approach
A Verrotti, P Fusilli, R Pallotta, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
November 1, 1983
[Pharmacological prevention of exercise-induced bronchospasm: review of the literature and trial of disodium cromoglycate, fenoterol and ipratropium bromide in a pediatric population]
M Verini, F Chiarelli, A Di Tullio, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
May 1, 1984
[Evaluation of the metacarpophalangeal profile (MPP) and of the dermatoglyphic pattern in Crouzon's syndrome]
R Pallotta, R Nardi, E Del Vomano, et al.
Acta Stomatologica Belgica
|
June 1, 1989
Enamel defects in a case of Menkes' syndrome
R Pallotta, F Del Rosso, S Domizio, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics
|
March 1, 1984
[Long-term effects of neonatal medium-degree hyperbilirubinemia on brainstem evoked potentials]
R Pallotta, M Minervino, G Sabatino, et al.
Clinical Genetics
|
November 1, 1996
Cerebral defects confirm midline developmental field disturbances in supernumerary der(22), t(11;22) syndrome
R Pallotta, P Fusilli, T Ehresmann, et al.
Page
of 3