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C Borrone

Showing results (11-20 of 89) with videos related to

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The British Journal of Dermatology|February 1, 1983
Trichothiodystrophy--BIDS, IBIDS and PIBIDS?F Crovato, C Borrone, A Rebora
The Journal of Pediatrics|December 1, 1986
Galactosemia caused by generalized uridine diphosphate galactose-4-epimerase deficiencyL Garibaldi, A Superti-Furga, C Borrone
Pathologica|March 1, 1973
[Phytohemagglutinine (PHA) skin test for early diagnosis of the lymphocyte T deficiency]C Borrone, F D Bricarelli, P Moscatelli
Annales De Genetique|September 1, 1971
[47,XX,18+-46,XX-45,XX,18- mosaicism in a child with Edward's syndrome]F D Bricarelli, F Gimelli, C Borrone
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1981
[Gaucher's disease. Longitudinal-study in 17 patients in a 10-year period (1970-1980) (author's transl)]M Di Rocco, D Salemi, C Borrone
Lancet (London, England)|February 12, 1977
Fucosidosis in Calabria: founder effect or high gene frequencyG Romeo, C Borrone, R Gatti, et al.
Lancet (London, England)|November 3, 1973
Letter: Genetic heterogeneity in fucosidosisR Gatti, C Borrone, X Trias, et al.
The Journal of Pediatrics|May 1, 1974
Fucosidosis: clinical, biochemical, immunologic, and genetic studies in two new casesC Borrone, R Gatti, X Trias, et al.
Pathologica|March 1, 1973
[Study of a case of severe complicated immunologic deficiency (agammaglobulinemia of the Swiss type)]C Borrone, M Governa, F D Bricarelli, et al.
European Journal of Pediatrics|June 1, 1991
Intracranial calcifications and nephrogenic diabetes insipidusM Di Rocco, P Picco, P Gandullia, et al.
Pageof 9

Showing results (11-20 of 89) with videos related to

Sort By:
Pageof 9
The British Journal of Dermatology|February 1, 1983
Trichothiodystrophy--BIDS, IBIDS and PIBIDS?F Crovato, C Borrone, A Rebora
The Journal of Pediatrics|December 1, 1986
Galactosemia caused by generalized uridine diphosphate galactose-4-epimerase deficiencyL Garibaldi, A Superti-Furga, C Borrone
Pathologica|March 1, 1973
[Phytohemagglutinine (PHA) skin test for early diagnosis of the lymphocyte T deficiency]C Borrone, F D Bricarelli, P Moscatelli
Annales De Genetique|September 1, 1971
[47,XX,18+-46,XX-45,XX,18- mosaicism in a child with Edward's syndrome]F D Bricarelli, F Gimelli, C Borrone
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|November 1, 1981
[Gaucher's disease. Longitudinal-study in 17 patients in a 10-year period (1970-1980) (author's transl)]M Di Rocco, D Salemi, C Borrone
Lancet (London, England)|February 12, 1977
Fucosidosis in Calabria: founder effect or high gene frequencyG Romeo, C Borrone, R Gatti, et al.
Lancet (London, England)|November 3, 1973
Letter: Genetic heterogeneity in fucosidosisR Gatti, C Borrone, X Trias, et al.
The Journal of Pediatrics|May 1, 1974
Fucosidosis: clinical, biochemical, immunologic, and genetic studies in two new casesC Borrone, R Gatti, X Trias, et al.
Pathologica|March 1, 1973
[Study of a case of severe complicated immunologic deficiency (agammaglobulinemia of the Swiss type)]C Borrone, M Governa, F D Bricarelli, et al.
European Journal of Pediatrics|June 1, 1991
Intracranial calcifications and nephrogenic diabetes insipidusM Di Rocco, P Picco, P Gandullia, et al.
Pageof 9