-
[文献書誌] Shimizu H,Suzumori K,Hatta N,Nishikawa T: "Absence of detectable α6 integrin in pyloric atresia-junctional epidermolysis bullosa syndrome and its application for prenatal diagnosis in a family at risk for recurrence" Arch Dermatol. 132. 919-925 (1996)
-
[文献書誌] Shimizu H,McGrath JA,Christiano AM,Nishikawa T,Uitto J: "Molecular basis of recessive dystrophic epidermolysis bullosa:genotype/phenotype correlation in a case of moderate clinical saverity" J Invest Dermatol. 106. 119-124 (1996)
-
[文献書誌] Shimizu H,Suzumori K,Nishikawa T: "Heterogeneous reactivity with LH7.2 and the first prenatal diagnosis of generalized recessive dystrophic epidermolysis bullosa amon Japanese patients" Dermatology. 192. 203-207 (1996)
-
[文献書誌] Pulkkinen L,Smith FJD,Shimizu H,Murata S,Yaoita H,Hachisuga H,Nishikawa T,McLean WHI,Uitto J: "Homozygous delection mutations in the plectin gene (PLEC1) in patients with epidermolysis bullosa simplex associated with late-onset muscular dystrophy" Hum Mol Genet. 5. 1539-1546 (1996)
-
[文献書誌] Shimizu H,Takizawa Y,McGrath JA,Pulkkinen L,Christiano AM,Uitto J,Burgeson RE,Iwatsuki K,Niimi N,Noguchi M,Imayama S,Abe Y,Shirakata Y,Hagiwara S,Saida R,Ogawa H,Hashimoto I,Nishikawa T: "Abesence of R42X and R635X mutations in the LAMB3 gene in 12 Japanese patients with junctional epidermolysis bullosa." Arch Dermatol Res (in press).
