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寻常型鱼鳞病并发多发性肌炎1例

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出处 《中国皮肤性病学杂志》 CAS 北大核心 2010年第6期582-583,共2页 The Chinese Journal of Dermatovenereology
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  • 1[1]Stoll C, Eyer D. A syndrome of congenital ichthyosis, hypogonadism, small stature, facial dysmorphism, scoliosis and myogenic dystrophy. Ann Genet, 1999,42:45
  • 2[2]Kaufman LM. A syndrome of retinitis pigmentosa, congenital ichthyosis, hypergonadotropic hypogonadism, small stature, mental retardation, cranial dysmorphism, and abnormal electroencephalogram. Ophthalmic Genet, 1998,19:69
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  • 5[5]Gohlke BC, Haug K, Fukami M, et al. Interstitial deletion in Xp22.3 is associated with X linked ichthyosis, mental retardation, and epilepsy. J Med Genet, 2000,37:600
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  • 8孙莉.神经纤维瘤病伴寻常型鱼鳞病1例.中国皮肤性病学杂志,1994,8(3):190-190.
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  • 10裴世澄,王天成.神经皮肤鱼鳞病家系研究[J].中国优生与遗传杂志,2000,8(5):107-107. 被引量:4

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