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Journal of Youth and Adolescence|December 5, 2013
Idiopathic precocious puberty in girls: Psychosexual developmentH F Meyer-Bahlburg, A A Ehrhardt, J J Bell, et al.
Spine|December 1, 1987
Cervical ligamentous instability in a canine in vivo modelR Whitehill, D J Moran, R E Fechner, et al.
Lancet (London, England)|May 26, 1979
Prenatal diagnosis of congenital adrenal hyperplasia (21-hydroxylase deficiency) by HLA typingM S Pollack, D Maurer, L S Levine, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1983
Genotyping steroid 21-hydroxylase deficiency: hormonal reference dataM I New, F Lorenzen, A J Lerner, et al.
The Journal of Steroid Biochemistry and Molecular Biology|June 1, 2001
Resistance to multiple steroids in two sistersM I New, S Nimkarn, D D Brandon, et al.
The Journal of Clinical Endocrinology and Metabolism|December 22, 1999
Resistance to several steroids in two sistersM I New, S Nimkarn, D D Brandon, et al.
The Journal of Clinical Endocrinology and Metabolism|December 13, 2003
A novel semiquantitative polymerase chain reaction/enzyme digestion-based method for detection of large scale deletions/conversions of the CYP21 gene and mutation screening in Turkish families with 21-hydroxylase deficiencyT Tukel, O Uyguner, J Q Wei, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1995
A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excessR C Wilson, Z S Krozowski, K Li, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 26, 1998
A genetic defect resulting in mild low-renin hypertensionR C Wilson, S Dave-Sharma, J Q Wei, et al.
IEEE Computer Graphics and Applications|October 23, 2020
Challenges in Evaluating Interactive Visual Machine Learning SystemsN Boukhelifa, A Bezerianos, R Chang, et al.
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