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

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

Original language	English
Pages (from-to)	787 - 788
Number of pages	2
Journal	Journal of Pediatric Endocrinology and Metabolism
Volume	24
DOIs	https://doi.org/10.1515/JPEM.2011.331
Publication status	Published - 2011

Cite this

@article{5def429df4ab47d78884a8616d111e3e,

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",

}

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 -