3Alhopuro P,Katajisto P,Lehtonan R.Mutation analysis of three genes encoding novel LKB1-interacting proteins,BRG1,STRADalpha,and MO25alpha,in Peutz-Jeghers syndrome[J].Br J Cancer,2005,92(6):1126-1129.
4Baker NL,Morgelin M,Peat R,et al.Dominant collagen Ⅵ mutations are a common cause of Ullrich congenital muscular dystrophy[J].Hum Mol Genet,2005,14(2):279-293.
5Lampe AK,Dunn DM,Von Niederhansern AC.Automated genomic sequence analysis of the three collagen Ⅵ genes:applications to Ullrich conganital muscular dystrophy and Bethlem myopathy[J].J Med Genet,2005,42(2):108-120.
6Peutz J L. A very remarkable case of familial polyposis of mucous menbrane of intesrinal tract and nasophary accompanied by peculiar pigmentation of skin and mu- cous membrane[J]. Ned Maandschr, 1921(10) : 134-146.
7Jeghers H, Mckusiek V A, Katz K H. Generalized intestinal polysosis and melanin spcts of the oral mucosa,lips and dig- its[J]. N Engl J Med,1949,241(25) :993-1005.
8Aretz S,Stienen D, Uhlhaas S. High proportion of large genonic STK dsletions in Peutz-Jeghers syndroms[J]. Hum Mutat,2005,26(6) :513-519.
9Peutz JL. A very remarkable ease of familial polyposis of mu- cous membrane of intesrinal tract and nasophary accompanied by peculiar pigmentation of skin and mucous membrane[J]. Ned Maandschr. 1921,10 : 134-146.
10Jeghers H, Mckusick VA, Katz KH. Generalized intestinal polyp- osis and melanin spcts of the oral mucosa, lips and digits[J]. N En- gl J Med, 1949, 241(25):993-1005.
