(Q43229970)

16 November 2017

Final diagnosis in children with subclinical hypothyroidism and mutation analysis of the thyroid peroxidase gene (TPO). (English)

1 reference

16 November 2017

Doga Turkkahraman

1

1 reference

16 November 2017

Ozgul M Alper

2

1 reference

16 November 2017

Funda Aydin

3

1 reference

16 November 2017

Akin Yildiz

4

1 reference

16 November 2017

Suray Pehlivanoglu

5

1 reference

16 November 2017

Guven Luleci

6

1 reference

16 November 2017

Sema Akcurin

7

1 reference

16 November 2017

Iffet Bircan

8

1 reference

16 November 2017

1 September 2009

1 reference

Journal of Pediatric Endocrinology and Metabolism

16 November 2017

1 reference

16 November 2017

22

1 reference

16 November 2017

9

1 reference

16 November 2017

845-851

1 reference

Definitive diagnosis in children with congenital hypothyroidism

16 November 2017

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.9.845

Three-year follow-up of borderline congenital hypothyroidism.

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.9.845

Defective organification of iodide causing hereditary goitrous hypothyroidism

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.9.845

Structure of the human thyroid peroxidase gene: comparison and relationship to the human myeloperoxidase gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.9.845

Thyroperoxidase gene mutations in congenital goitrous hypothyroidism with total and partial iodide organification defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.9.845

Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.9.845

Pendred syndrome: evidence for genetic homogeneity and further refinement of linkage

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.9.845

A rapid non-enzymatic method for the preparation of HMW DNA from blood for RFLP studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.9.845

High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.9.845

Persistent mild hypothyroidism associated with novel sequence variants of the DUOX2 gene in two siblings

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.9.845

Identification of five novel inactivating mutations in the human thyroid peroxidase gene by denaturing gradient gel electrophoresis

21 January 2018

1 reference

https://api.crossref.org/works/10.1515%2FJPEM.2009.22.9.845

10.1515/JPEM.2009.22.9.845

21 January 2018

Identifiers

DOI

1 reference

16 November 2017

1 reference