| Keywords: |
child; review; follow up; follow-up studies; metabolism; heredity; genotype; risk; pedigree; infant, newborn; diagnostic errors; diagnosis; newborn; diagnostic error; pregnancy; sodium; medical ethics; therapy; fetal diseases; enzyme deficiency; endocrine system; etiology; histocompatibility testing; histocompatibility test; nutritional deficiency; fetus disease; prenatal diagnosis; ethics, medical; amnion fluid; human; male; female; priority journal; article; support, u.s. gov't, p.h.s.; steroid hydroxylases; congenital adrenal hyperplasia; congenital disorder; steroid 21 monooxygenase deficiency; adrenal hyperplasia, congenital; amniotic fluid; 17-hydroxyprogesterone; hydroxyprogesterones; hydroxyprogesterone; progesterone derivative; steroid monooxygenase
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