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L Beccaria

Showing results (41-50 of 45) with videos related to

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European Journal of Pediatrics|April 15, 2003
Hypogonadism and pubertal development in Prader-Willi syndromeA Crinò, R Schiaffini, P Ciampalini, et al.
American Journal of Human Genetics|July 1, 1997
Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndromeR Carrozzo, E Rossi, S L Christian, et al.
Annali Dell'Istituto Superiore Di Sanita|January 25, 2000
[Prader-Willi syndrome]L Beccaria, L Bosio, F Benzi, et al.
The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defectsM Muzza, S Rabbiosi, M C Vigone, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 22, 2009
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signsA Crinò, G Di Giorgio, C Livieri, et al.
Pageof 5

Showing results (41-50 of 45) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 45 results.
European Journal of Pediatrics|April 15, 2003
Hypogonadism and pubertal development in Prader-Willi syndromeA Crinò, R Schiaffini, P Ciampalini, et al.
American Journal of Human Genetics|July 1, 1997
Inter- and intrachromosomal rearrangements are both involved in the origin of 15q11-q13 deletions in Prader-Willi syndromeR Carrozzo, E Rossi, S L Christian, et al.
Annali Dell'Istituto Superiore Di Sanita|January 25, 2000
[Prader-Willi syndrome]L Beccaria, L Bosio, F Benzi, et al.
The Journal of Clinical Endocrinology and Metabolism|January 16, 2014
The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defectsM Muzza, S Rabbiosi, M C Vigone, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 22, 2009
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signsA Crinò, G Di Giorgio, C Livieri, et al.
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