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Citation: J. Frank et al., Characterization of the desmosomal cadherin gene family: Genomic organization of two desmoglein genes on human chromosome 18q12, EXP DERMATO, 10(2), 2001, pp. 90-94
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Citation: Pb. Cserhalmi-friedman et al., Structural analysis reflects the evolutionary relationship between the human desmocollin gene family members, EXP DERMATO, 10(2), 2001, pp. 95-99
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Citation: J. Miller et al., Atrichia caused by mutations in the vitamin D receptor gene is a phenocopyof generalized atrichia caused by mutations in the hairless gene, J INVES DER, 117(3), 2001, pp. 612-617
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Citation: J. Frank et al., A spectrum of novel mutations in the protoporphyrinogen oxidase gene in 13families with variegate porphyria, J INVES DER, 116(5), 2001, pp. 821-823
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Citation: Pb. Cserhalmi-friedman et al., Diagnosis of autosomal recessive lamellar ichthyosis with mutations in theTGM1 gene, BR J DERM, 144(4), 2001, pp. 726-730
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Citation: Pb. Cserhalmi-friedman et al., Structural analysis and mutation detection strategy for the human LamC3 gene, BIOC BIOP R, 280(1), 2001, pp. 39-44
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Citation: J. Frank et al., Identification of a founder mutation in the protoporphyrinogen oxidase gene in variegate porphyria patients from Chile, HUMAN HERED, 51(3), 2001, pp. 160-168
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Citation: Pb. Cserhalmi-friedman et al., Preimplantation genetic diagnosis in two families at risk for recurrence of Herlitz junctional epidermolysis bullosa, EXP DERMATO, 9(4), 2000, pp. 290-297
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Citation: Aa. Panteleyev et al., Ornithine decarboxylase transgenic mice as a model for human atrichia withpapular lesions, EXP DERMATO, 9(2), 2000, pp. 146-151
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Citation: Vm. Aita et al., A novel missense mutation (C622G) in the zinc-finger domain of the human hairless gene associated with congenital atrichia with papular lesions, EXP DERMATO, 9(2), 2000, pp. 157-162
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Citation: Aa. Panteleyev et al., The bulge is the source of cellular renewal in the sebaceous gland of mouse skin, ARCH DERM R, 292(11), 2000, pp. 573-576