Oliver-Petit_2021_Front.Endocrinol.(Lausanne)_12_657913

Reference

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

Related information

Citations formats

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