Title : Next-Generation Sequencing Analysis Reveals Frequent Familial Origin and Oligogenism in Congenital Hypothyroidism With Dyshormonogenesis - Oliver-Petit_2021_Front.Endocrinol.(Lausanne)_12_657913 |
Author(s) : Oliver-Petit I , Edouard T , Jacques V , Bournez M , Cartault A , Grunenwald S , Savagner F |
Ref : Front Endocrinol (Lausanne) , 12 :657913 , 2021 |
Abstract : Oliver-Petit_2021_Front.Endocrinol.(Lausanne)_12_657913 |
ESTHER : Oliver-Petit_2021_Front.Endocrinol.(Lausanne)_12_657913 |
PubMedSearch : Oliver-Petit_2021_Front.Endocrinol.(Lausanne)_12_657913 |
PubMedID: 34248839 |
Oliver-Petit I, Edouard T, Jacques V, Bournez M, Cartault A, Grunenwald S, Savagner F (2021)
Next-Generation Sequencing Analysis Reveals Frequent Familial Origin and Oligogenism in Congenital Hypothyroidism With Dyshormonogenesis
Front Endocrinol (Lausanne)
12 :657913
Oliver-Petit I, Edouard T, Jacques V, Bournez M, Cartault A, Grunenwald S, Savagner F (2021)
Front Endocrinol (Lausanne)
12 :657913