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Volumn 29, Issue 3, 2010, Pages 191-196
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21-hydroxylase deficiency congenital adrenal hyperplasia.
a
a
NONE
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Author keywords
[No Author keywords available]
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Indexed keywords
DEXAMETHASONE;
STEROID 21 MONOOXYGENASE;
CONGENITAL ADRENAL HYPERPLASIA;
FEMALE;
GENETICS;
GENOTYPE;
HUMAN;
MALE;
NEWBORN;
NUCLEOTIDE SEQUENCE;
NURSING;
NURSING DIAGNOSIS;
PATHOPHYSIOLOGY;
PHYSIOLOGY;
PRECOCIOUS PUBERTY;
PREGNANCY;
PRENATAL CARE;
RENIN ANGIOTENSIN ALDOSTERONE SYSTEM;
REVIEW;
ADRENAL HYPERPLASIA, CONGENITAL;
DEXAMETHASONE;
DNA MUTATIONAL ANALYSIS;
FEMALE;
GENOTYPE;
HUMANS;
INFANT, NEWBORN;
MALE;
NURSING DIAGNOSIS;
PREGNANCY;
PRENATAL CARE;
PUBERTY, PRECOCIOUS;
RENIN-ANGIOTENSIN SYSTEM;
STEROID 21-HYDROXYLASE;
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EID: 77957310332
PISSN: None
EISSN: 15392880
Source Type: Journal
DOI: 10.1891/0730-0832.29.3.191 Document Type: Review |
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Times cited : (4)
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References (14)
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