Search research articles
Contact Us
Filters
Showing results (11-20 of 13) with videos related to
Page
of 2
Sort By:
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 mutations
H 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 KCNJ11
J 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 paper
J Bacchetta, T Edouard, G Laverny, et al.
Page
of 2
Search research articles
Search
Showing results (11-20 of 13) with videos related to
Sort By:
Page
of 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 mutations
H 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 KCNJ11
J 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 paper
J Bacchetta, T Edouard, G Laverny, et al.
Page
of 2