reference/9905973

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9905973

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endingPage	4536
issn	1945-7197 0021-972X
issueIdentifier	11
pageRange	4528-4536
publicationName	The Journal of clinical endocrinology and metabolism
startingPage	4528
bibliographicCitation	Sobrier ML, Maghnie M, Vié-Luton MP, Secco A, di Iorgi N, Lorini R, Amselem S. Novel HESX1 mutations associated with a life-threatening neonatal phenotype, pituitary aplasia, but normally located posterior pituitary and no optic nerve abnormalities. J Clin Endocrinol Metab. 2006 Nov;91(11):4528–36. doi: 10.1210/jc.2006-0426. PMID: 16940453.
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date	2006-11-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/16940453 https://doi.org/10.1210/jc.2006-0426
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language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Novel HESX1 Mutations Associated with a Life-Threatening Neonatal Phenotype, Pituitary Aplasia, but Normally Located Posterior Pituitary and No Optic Nerve Abnormalities
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