Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders

6533b7d4fe1ef96bd1262826

RESEARCH PRODUCT

Mutations in the NKX2.1 and the PAX8 genes in a boy with thyroid dysgenesis, respiratory and neurological disorders

Joachim Pohlenz Małgorzata Kumorowicz-czoch Pia Hermanns

subject

Pediatrics medicine.medical_specialty business.industry Pediatric research education Bioinformatics medicine.disease Thyroid dysgenesis Diabetes mellitus Meeting Abstract medicine Respiratory system business PAX8

description

s of the 51st Workshop for Pediatric Research 51st Workshop for Pediatric Research Gottingen, Germany

year	journal	country	edition	language
2015-07-01	Molecular and Cellular Pediatrics

10.1186/2194-7791-2-s1-a9 http://europepmc.org/articles/PMC4715207

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