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Showing results (11-20 of 13) with videos related to

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European Journal of Endocrinology|September 13, 2014
Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutationsH E Ramos, A Carré, L Chevrier, et al.
The American Journal of Pathology|June 8, 2001
Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11J C Fournet, C Mayaud, P de Lonlay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 20, 2022
Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paperJ Bacchetta, T Edouard, G Laverny, et al.
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Showing results (11-20 of 13) with videos related to

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Pageof 2
You have reached the last page of results.This site can display upto 13 results.
European Journal of Endocrinology|September 13, 2014
Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutationsH E Ramos, A Carré, L Chevrier, et al.
The American Journal of Pathology|June 8, 2001
Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11J C Fournet, C Mayaud, P de Lonlay, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 20, 2022
Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paperJ Bacchetta, T Edouard, G Laverny, et al.
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