Amanote Research

Amanote Research

    RegisterSign In

DUOX Defects and Their Roles in Congenital Hypothyroidism

Methods in Molecular Biology - United States
doi 10.1007/978-1-4939-9424-3_37
Full Text
Open PDF
Abstract

Available in full text

Categories
GeneticsMolecular Biology
Date

January 1, 2019

Authors
Xavier De DekenFrançoise Miot
Publisher

Springer New York


Related search

Structural Defects of a Pax8 Mutant That Give Rise to Congenital Hypothyroidism

Biochemical Journal
BiochemistryCell BiologyMolecular Biology
1999English

Primary Congenital Hypothyroidism

2020English

Transient Congenital Hypothyroidism

Archives of Disease in Childhood
Child HealthPediatricsPerinatology
1987English

Congenital Hypothyroidism: Update and Perspectives

European Journal of Endocrinology
MedicineEndocrinologyMetabolismDiabetes
2018English

Screening for Congenital Hypothyroidism

Pediatric Research
Child HealthPediatricsPerinatology
1975English

Factors Associated With Permanent Hypothyroidism in Infants With Congenital Hypothyroidism

BMC Pediatrics
Child HealthPediatricsPerinatology
2019English

Screening for Congenital Hypothyroidism.

Archives of Disease in Childhood
Child HealthPediatricsPerinatology
1980English

Screening for Congenital Hypothyroidism.

BMJ
1980English

Congenital Defects in Mongols

BMJ
1952English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy