[an error occurred while processing this directive] ����Ƥ���Բ�ѧ��־ 2005, 31(4) 223-225 DOI:     ISSN: 2096-5540 CN: 32-1880/R

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1. �Ͼ�ҽ�ƴ�ѧ���������ڶ�ҽԺ�������еڶ�����ҽԺƤ����, ����214002;
2. ����ҽ�ƴ�ѧ��һ����ҽԺƤ���ơ�����ҽ�ƴ�ѧƤ�����о���

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2. ����ҽ�ƴ�ѧ��һ����ҽԺƤ���ơ�����ҽ�ƴ�ѧƤ�����о���

Abstract:

Keywords:
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[2] Emmert S, Kuster W, Hennies HC, et al. 47 patients in 14 families with the rare genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer. Eur J Dermatol, 2003, 13:16-20.
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[13] Lee YG, Macoska JA, Korenchuk S,et al. MIM, a potential metastasis suppressor gene in bladder cancer. Neoplasia, 2002, 4: 291-294.
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[15] Powell FC, Venencie PY, Gordon H, et al. Keratoderma and spastic paralysis. Br J Dermatol, 1983, 109:589-596.
[16] Gamborg Nielsen P. Punctate palmoplantar keratoderma associated with morbus Bechterew and HLA B 27. A family study. Acta Derm Venereol, 1988, 68:346-350.
[17] Salamon T, Stolic V, Lazovic-Tepavac O, et al. Peculiar findings in a family with keratodermia palmo-plantaris papulosa Buschke-FischerBrauer. Hum Genet, 1982, 60:314-319.
[18] Emmert S, Kuster W, Zutt M, et al. A new family with the rare genodermatosis keratosis punctata palmoplantaris Buschke-Fischer-Brauer.J Am Acad Dermatol, 2003, 49:1166-1169.
[19] Asadi AK. Type �� hereditary punctate keratoderma. Dermatol OnlineJ, 2003, 9:38.
[20] Kelsell DP, Stevens HP. The palmoplantar keratodermas: much more than palms and soles. Mol Med Today,1999, 5:107-113.
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