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XERODERMA PIGMENTOSUM

Archives of Dermatology and Syphilology, 1932
The patient whose case of xeroderma pigmentosum is reported in this paper presented an unusual clinical picture, and the diagnosis was definitely established only after histopathologic studies had been made. Certain histopathologic features which we consider diagnostic of the disease will be emphasized. Finally, some of the clinical and histopathologic
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XERODERMA PIGMENTOSUM

Archives of Dermatology and Syphilology, 1944
Haldane has described a method of inheritance which he has called incomplete sex linkage, in contrast to the mode of inheritance exhibited by hemophilia, for example, which is said to be fully sex linked. Xeroderma pigmentosum is one of the diseases said by Haldane to show incomplete sex linkage.
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XERODERMA PIGMENTOSUM

Archives of Dermatology and Syphilology, 1945
After the publication of the article on xeroderma pigmentosum which appeared in the March 1944 issue of theArchives, 1 Dr. Gaumond, of the city of Quebec, called my attention to a family on which he had first reported in 1934 2 and again, with Dr. Mayrand, in 1936 3 and in which there were 6 children affected with this disease.
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XERODERMA PIGMENTOSUM

British Journal of Dermatology, 1973
V M, Der Kaloustian, A K, Kurban
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Xeroderma pigmentosum variants

Cytogenetic and Genome Research, 1981
J E, Cleaver   +3 more
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Xeroderma Pigmentosum

International Journal of Dermatology, 1986
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Xeroderma pigmentosum

2022
Luh Made Mas Rusyati   +4 more
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Xeroderma pigmentosum

British Journal of Plastic Surgery, 1992
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[Xeroderma pigmentosum].

Geka chiryo. Surgical therapy, 1969
H, Hatano, M, Okido
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