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家族性Kallmann综合征亚型3例报告 被引量:3

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出处 《中国男科学杂志》 CAS CSCD 2000年第2期129-130,共2页 Chinese Journal of Andrology
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参考文献5

  • 1Rugarli EL, Ballabio A. Kallmann syndrome from genetics to neurobiology. JAMA 1993 ;270:2713
  • 2新刘民主编.实用内分泌学.第2版.北京:人民军医出版社,1997;653-656
  • 3邓春华,梅骅,苗永青.Kallmann 综合征四例报告[J].中华泌尿外科杂志,1997,18(5):298-300. 被引量:13
  • 4Tompach PC, Zeitler DL. Kallmann syndrome with associated cleftlip and palate: case report and review of the literautre, J Oral Maxillofac Surg 1995; 53 :85
  • 5南勋义,李永海,党建功,刘润明,邢俊平,王明珠.非典型性Kallmann综合征[J].中华泌尿外科杂志,1999,20(2):118-119. 被引量:5

二级参考文献3

  • 1邓春华,中华泌尿外科杂志,1997年,18卷,298页
  • 2刘新民,实用内分泌学(第2版),1997年,653页
  • 3黄平治,男性性功能障碍,1992年,122页

共引文献15

同被引文献31

  • 1华咏(综述),杨建华(审校).Kallmann综合征的研究进展[J].中国男科学杂志,2005,19(4):64-66. 被引量:5
  • 2Tompach PC, Zeitler DL. Kallmann syndrome with associated cleft lip and palate: case report and review of the literature. J Oral Maxillofac Surg 1995; 53(1): 85-87.
  • 3Hardelin JP, Dod e C. The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et al, Sex Dev 2008; 2(4-5): 181-193.
  • 4Dod e C, Hardelin JP. Kallmann syndrome. Eur J Hum Genet 2009; 17(2): 139-146.
  • 5Cole LW, Sidis Y, Zhang C, et al. Mutations in prokineticin 2 and prokineticin receptor 2 genes in human gonadotrophin- releasing hormone deficiency: molecular genetics and clinical spectrum. J Clin Endocrinol Metab 2008; 93 (9): 3551-3559.
  • 6Tole S, Gutin G, Bhatnagar L, et al. Development of midline cell types and commissural axon tracts requires Fgfrl in the cerebrum. Dev Biol 2006; 289(1): 141-151.
  • 7Schwankhaus JD, Currie J, Jaffe MJ, et al. Neurologic findings in men with isolated hypogonadotropic hypogonadism. Neurology 1989;39(2 Pt 1): 223-226.
  • 8Reardon W. Kallmann syndrome presenting as congenital ptosis in brothers. Clin Dysmorpho12007; 16(3): 207-208.
  • 9Coatesworth AP, Woodhead CJ .Conductive hearing loss associated with Kallmann's syndrome. J Laryngol Otol 2002; 116(2): 125-126.
  • 10Kirk JM, Grant DB, Besser GM, et al. Unilateral renal aplasia in X-linked Kallmann's syndrome. Clin Genet 1994; 46(3): 260-262.

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二级引证文献6

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