Ji-QingWeiMD

PubMed

• 35 citations
  Genotyping of Five Chinese Patients with 17α-Hydroxylase Deficiency Diagnosed through High-Performance Liquid Chromatography Serum Adrenal Profile: Identification of T...
  Ji-Qing Wei, Ji-Lu Wei, Wei-Chun Li, Yun-Sheng Bi, Feng-Cai Wei> ;The Journal of Clinical Endocrinology and Metabolism. 2006 Sep 1
• 5 citations
  Nonclassic 21-hydroxylase deficiency in Croatia.
  Miroslav Dumić, Jasenka Ille, Zunec R, Vesna Plavšić, Igor Francetić, Veselin Škrabić, Nevena Janjanin, Anita Spehar, Ji-Qing Wei, Robert C. Wilson, Maria I. New> ;Journal of Pediatric Endocrinology & Metabolism. 2004 Jan 1
• 107 citations
  A genetic defect resulting in mild low-renin hypertension.
  Robert C. Wilson, Swati Dave-Sharma, Ji-Qing Wei, Varuni R. Obeyesekere, Kevin X. Z. Li, Paolo Ferrari, Zygmunt S. Krozowski, Cedric H. L. Shackleton, Leon Bradlow, Ti...> ;Proceedings of the National Academy of Sciences of the United States of America. 1998 Aug 18
• 140 citations
  Examination of genotype and phenotype relationships in 14 patients with apparent mineralocorticoid excess.
  Swati Dave-Sharma, Robert C. Wilson, Madeleine D. Harbison, Ron S. Newfield, Maryam Razzaghy Azar, Zygmunt S. Krozowski, John W. Funder, Cedric H. L. Shackleton, H. Le...> ;The Journal of Clinical Endocrinology and Metabolism. 1998 Jul 1
• 120 citations
  Several homozygous mutations in the gene for 11 beta-hydroxysteroid dehydrogenase type 2 in patients with apparent mineralocorticoid excess.
  Robert C. Wilson, Madeleine D. Harbison, Zygmunt S. Krozowski, John W. Funder, C. H. L. Shackleton, H M Hanauske-Abel, Ji-Qing Wei, J Hertecant, Antoinette Moran, Rich...> ;The Journal of Clinical Endocrinology and Metabolism. 1995 Nov 1
• 167 citations
  A mutation in the HSD11B2 gene in a family with apparent mineralocorticoid excess
  Robert C. Wilson, Zygmunt S. Krozowski, K. Li, V. R. Obeyesekere, Maryam Razzaghy-Azar, Madeleine D. Harbison, Ji-Qing Wei, C. H. L. Shackleton, John W. Funder, Maria ...> ;The Journal of Clinical Endocrinology and Metabolism. 1995 Jul 1
• 130 citations
  Prenatal treatment and diagnosis of congenital adrenal hyperplasia owing to steroid 21-hydroxylase deficiency.
  A. B. Mercado, Robert C. Wilson, K. C. Cheng, Ji-Qing Wei, Maria I. New> ;The Journal of Clinical Endocrinology and Metabolism. 1995 Jul 1
• 110 citations
  Rapid deoxyribonucleic acid analysis by allele-specific polymerase chain reaction for detection of mutations in the steroid 21-hydroxylase gene.
  Robert C. Wilson, Ji-Qing Wei, K. C. Cheng, A. B. Mercado, Maria I. New> ;The Journal of Clinical Endocrinology and Metabolism. 1995 May 1
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