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

Atul Malhotra, Philip Bruce Bergman, Justin Brown, George McGillivray

Research output: Contribution to journalArticleOtherpeer-review

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

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title = "Congenital hypothyroidism in association with chromosome 3p25.3-pter deletion",
abstract = "This is the first reported case of congenital hypothroidism in an infant with chromosome 3p deletion.",
author = "Atul Malhotra and Bergman, {Philip Bruce} and Justin Brown and George McGillivray",
year = "2011",
doi = "10.1515/JPEM.2011.331",
language = "English",
volume = "24",
pages = "787 -- 788",
journal = "Journal of Pediatric Endocrinology and Metabolism",
issn = "0334-018X",
publisher = "Walter de Gruyter",

}

Congenital hypothyroidism in association with chromosome 3p25.3-pter deletion. / Malhotra, Atul; Bergman, Philip Bruce; Brown, Justin; McGillivray, George.

In: Journal of Pediatric Endocrinology and Metabolism, Vol. 24, 2011, p. 787 - 788.

Research output: Contribution to journalArticleOtherpeer-review

TY - JOUR

T1 - Congenital hypothyroidism in association with chromosome 3p25.3-pter deletion

AU - Malhotra, Atul

AU - Bergman, Philip Bruce

AU - Brown, Justin

AU - McGillivray, George

PY - 2011

Y1 - 2011

N2 - This is the first reported case of congenital hypothroidism in an infant with chromosome 3p deletion.

AB - This is the first reported case of congenital hypothroidism in an infant with chromosome 3p deletion.

U2 - 10.1515/JPEM.2011.331

DO - 10.1515/JPEM.2011.331

M3 - Article

VL - 24

SP - 787

EP - 788

JO - Journal of Pediatric Endocrinology and Metabolism

JF - Journal of Pediatric Endocrinology and Metabolism

SN - 0334-018X

ER -