CrossRef Text and Data Mining
Result of CrossRef Text and Data Mining Search is the related articles with entitled article. If you click link1 or link2 you will be able to reach the full text site of selected articles; however, some links do not show the full text immediately at now. If you click CrossRef Text and Data Mining Download icon, you will be able to get whole list of articles from literature included in CrossRef Text and Data Mining.
Persistent goiter with congenital hypothyroidism due to mutation in DUOXA2 gene
So Yoon Jung, Jeongho Lee, Dong Hwan Lee
Ann Pediatr Endocrinol Metab. 2020;25(1):57-62.   Published online March 31, 2020
DOI: https://doi.org/10.6065/apem.2020.25.1.57

Excel Download

Persistent goiter with congenital hypothyroidism due to mutation in DUOXA2 gene
Annals of Pediatric Endocrinology & Metabolism. 2020;25(1):57-62   Crossref logo
Link1 Link2 Link3

Dyshormonogenetic goiter-like changes in a child with congenital hypothyroidism and a euthyroid adult
Diagnostic Cytopathology. 2012;41(8):720-724   Crossref logo
Link1 Link2

MON-265 Congenital Hypothyroidism and Bilateral Ptosis Due to a Novel TSHR Gene Mutation
Journal of the Endocrine Society. 2019;3(Supplement_1):   Crossref logo
Link1

Congenital Goiter with Hypothyroidism Caused by a 5′ Splice Site Mutation in the Thyroglobulin Gene
Thyroid. 2001;11(7):685-690   Crossref logo
Link1

Respiratory insufficiency in a newborn with congenital hypothyroidism due to a new mutation of TTF-1/NKX2.1 gene
Pediatric Pulmonology. 2013;49(3):E42-E44   Crossref logo
Link1 Link2

Mutation Screening of DUOX2 Gene in Children with Congenital Hypothyroidism
. 2020;   Crossref logo
Link1 Link2

Congenital hypothyroidism due to thyroglobulin deficiency: a case report with a novel mutation in TG gene
Annals of Pediatric Endocrinology & Metabolism. 2019;24(3):199-202   Crossref logo
Link1 Link2 Link3

Congenital Central Hypothyroidism due to a Homozygous Mutation in theTSHβSubunit Gene
Case Reports in Pediatrics. 2011;2011:1-4   Crossref logo
Link1 Link2 Link3

Clinical and Genetic Analysis of a Compound Heterozygous Mutation in the Thyroglobulin Gene in a Chinese Twin Family With Congenital Goiter and Hypothyroidism
Twin Research and Human Genetics. 2012;15(1):126-132   Crossref logo
Link1

Congenital dyshormonogenic hypothyroidism with goiter caused by a sodium/iodide symporter (SLC5A5) mutation in a family of Shih-Tzu dogs
Domestic Animal Endocrinology. 2018;65:1-8   Crossref logo
Link1 Link2