Congenital hypothyroidism in association with chromosome 3p25.3-pter deletion

Research output: Contribution to journalArticleOtherpeer-review

4 Citations (Scopus)

Abstract

This is the first reported case of congenital hypothroidism in an infant with chromosome 3p deletion.
Original languageEnglish
Pages (from-to)787 - 788
Number of pages2
JournalJournal of Pediatric Endocrinology and Metabolism
Volume24
DOIs
Publication statusPublished - 2011

Cite this