当前位置: 首页 > 期刊 > 《健康前沿》 > 20172
编号:13621007
Kartageners综合征一例(2)
http://www.100md.com 2017年1月15日 《健康前沿》 20172
     [2] Geremek M,Zietkiewicz E,Diehl SR,et al. Linkage analysis localises a Kartagener syndrome gene to a 3.5 c M region on chromosome 15q24-25[J]. J Med Genet,2006,43(1):e1.

    [3] Masud IU,Din SU. Kartagener's Syndrome[J]. Gom J Med Sci. 2006;4(2):79-81.

    [4] Olbrich H,Haffnex K,Kispert A,Volkel A,Volz A,Sasmaz G,et al. Mutation in DNA H5 cause primary cilliary dyskinesia and randomization of left right asymmetry[J]. Nature Genet. 2002;30:143-144.

    [5] None PG,Bali D,Carson JL,et al. Discordant organ laterality in monozygotic twins with primary cilliary dyskinesis[J]. Am J Med Genet. 1999;82:155-160.

    [6] Gregory T,Weinberger SE. Bronchiectasis and Lung abscess[J]. Harrison's Principles of Internal Medicine.(17th. Edition)II:1629-1632.

    [7] Eavey RD,Nadol JB,Jr,Holmes LB,Laird NM,Lapey A,Joseph MP,et al. Kartagener's Syndrome:A blinded controlled study of cilia ultrastructure[J].Arch Otolaryng Head Neck Surg. 1986;112:646-650.

    [8] Guerrant JL,Douty T,Tegtmeyer C,Jahrsdoerfer RA. Bronchiectasis in the immotile cilia syndrome[J]. New Eng J Med. 1978;298:282.

    [9] Meeks M,Bush A. Primaryciliarydyskinesia(PCD)[J]. PediatriPul-monology. 2000,29:307-316.

    [10] Leigh MW,Pittman JE,Carson JL,et al. Clinical and genetic aspects of primary ciliary dyskinesia/ Kartagener syndrome[J]. Genet Med. 2009,11(7):473-487.

    [11] Seaton D. Bronchiectasis[J]. Crofton and Douglas's respiratory disease.(5th edition)2000;1:794-828.

    [12] Greenstone M,Newman-Tailor A,Cole P. Bronchiectasis and oligospermia:two families[J]. Thorax. 1986;41:80., 百拇医药(金威 马娟娟)
上一页1 2