Abstract
| Original language | English |
|---|---|
| Pages (from-to) | 787 - 788 |
| Number of pages | 2 |
| Journal | Journal of Pediatric Endocrinology and Metabolism |
| Volume | 24 |
| DOIs | |
| Publication status | Published - 2011 |
Cite this
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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 journal › Article › Other › peer-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 -