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Nonclassic 21-hydroxylase deficiency in Croatia.
Dumic M, Ille J, Zunec R, Plavsic V, Francetic I, Skrabic V, Janjanin N, Spehar A, Wei J, Wilson RC, New MI. Dumic M, et al. J Pediatr Endocrinol Metab. 2004 Feb;17(2):157-64. doi: 10.1515/jpem.2004.17.2.157. J Pediatr Endocrinol Metab. 2004. PMID: 15055349
Prenatal diagnosis for congenital adrenal hyperplasia in 532 pregnancies.
New MI, Carlson A, Obeid J, Marshall I, Cabrera MS, Goseco A, Lin-Su K, Putnam AS, Wei JQ, Wilson RC. New MI, et al. Among authors: wei jq. J Clin Endocrinol Metab. 2001 Dec;86(12):5651-7. doi: 10.1210/jcem.86.12.8072. J Clin Endocrinol Metab. 2001. PMID: 11739415
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 deficiency.
Tukel T, Uyguner O, Wei JQ, Yuksel-Apak M, Saka N, Song DX, Kayserili H, Bas F, Gunoz H, Wilson RC, New MI, Wollnik B. Tukel T, et al. Among authors: wei jq. J Clin Endocrinol Metab. 2003 Dec;88(12):5893-7. doi: 10.1210/jc.2003-030813. J Clin Endocrinol Metab. 2003. PMID: 14671187
Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess.
Dave-Sharma S, Wilson RC, Harbison MD, Newfield R, Azar MR, Krozowski ZS, Funder JW, Shackleton CH, Bradlow HL, Wei JQ, Hertecant J, Moran A, Neiberger RE, Balfe JW, Fattah A, Daneman D, Akkurt HI, De Santis C, New MI. Dave-Sharma S, et al. Among authors: wei jq. J Clin Endocrinol Metab. 1998 Jul;83(7):2244-54. doi: 10.1210/jcem.83.7.4986. J Clin Endocrinol Metab. 1998. PMID: 9661590
70 results