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G Chiumello

Showing results (211-220 of 214) with videos related to

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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.
Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiencyL S Levine, B Dupont, F Lorenzen, et al.
Pageof 22

Showing results (211-220 of 214) with videos related to

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You have reached the last page of results.This site can display upto 214 results.
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.
Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiencyL S Levine, B Dupont, F Lorenzen, et al.
Pageof 22