MOLECULAR PATHOGENESIS OF CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) AND X-LINKED ADRENAL HYPOPLASIA CONGENITA

Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/158650

DC Field	Value
dc.title	MOLECULAR PATHOGENESIS OF CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) AND X-LINKED ADRENAL HYPOPLASIA CONGENITA
dc.contributor.author	LOKE KAH YIN
dc.date.accessioned	2019-09-16T00:39:39Z
dc.date.available	2019-09-16T00:39:39Z
dc.date.issued	2001
dc.identifier.citation	LOKE KAH YIN (2001). MOLECULAR PATHOGENESIS OF CONGENITAL ADRENAL HYPERPLASIA (21-HYDROXYLASE DEFICIENCY) AND X-LINKED ADRENAL HYPOPLASIA CONGENITA. ScholarBank@NUS Repository.
dc.identifier.uri	https://scholarbank.nus.edu.sg/handle/10635/158650
dc.source	CCK BATCHLOAD 20190911
dc.type	Thesis
dc.contributor.department	PAEDIATRICS
dc.contributor.supervisor	WONG HOCK BOON
dc.description.degree	Ph.D
dc.description.degreeconferred	DOCTOR OF MEDICINE
Appears in Collections:	Ph.D Theses (Restricted)

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