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The Journal of Clinical Endocrinology and Metabolism|March 20, 1999
Normal female infants born of mothers with classic congenital adrenal hyperplasia due to 21-hydroxylase deficiencyJ C Lo, V M Schwitzgebel, J B Tyrrell, et al.
The Journal of Rheumatology|December 1, 1993
Cooccurrence of collagenous colitis with seronegative spondyloarthropathy: report of a case and literature reviewS F Kingsmore, D B Kingsmore, B D Hall, et al.
American Journal of Medical Genetics|January 1, 1978
Normal intelligence in two children with Carpenter syndromeJ L Frias, A H Felman, A L Rosenbloom, et al.
The Journal of Pediatrics|August 7, 2001
The subtle facial signs of prenatal exposure to alcohol: an anthropometric approachE S Moore, R E Ward, P L Jamison, et al.
American Journal of Medical Genetics|March 1, 1993
Pleiotropy in Coffin-Lowry syndrome: sensorineural hearing deficit and premature tooth loss as early manifestationsJ K Hartsfield, B D Hall, A W Grix, et al.
The Journal of Clinical Endocrinology and Metabolism|July 1, 1985
Treatment of true precocious puberty with a potent luteinizing hormone-releasing factor agonist: effect on growth, sexual maturation, pelvic sonography, and the hypothalamic-pituitary-gonadal axisD M Styne, D A Harris, C A Egli, et al.
Nature|June 11, 1981
Only one of two closely related yeast suppressor tRNA genes contains an intervening sequenceM V Olson, G S Page, A Sentenac, et al.
Clinical Genetics|May 1, 1979
Partial trisomy for the distal long arm of chromosome 5 (region q34 leads to qter). A new clinically recognizable syndromeC J Curry, W D Loughman, U Francke, et al.
The Journal of Rheumatology|September 1, 1993
Presentation of multicentric Castleman's disease with sicca syndrome, cardiomyopathy, palmar and plantar rashS F Kingsmore, O E Silva, B D Hall, et al.
Archives of Surgery (Chicago, Ill. : 1960)|October 1, 1989
Medullary thyroid carcinoma. The need for early diagnosis and total thyroidectomyQ Y Duh, J J Sancho, F S Greenspan, et al.
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