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Authors:
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Lefevre, P
Rochat, A
Bodemer, C
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Barrandon, Y
de Prost, Y
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Hovnanian, A
Citation: P. Lefevre et al., Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusionof 10 genes including the hairless gene by mutation analysis, EUR J HUM G, 8(4), 2000, pp. 273-279
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Hamel-Teillac, D
Acar, P
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de Prost, Y
Citation: C. Buzenet et al., Facial hemangioma associated with arterial anomalies, coarctation of the aorta, and eye abnormalities: PHACES syndrome., ANN DER VEN, 127(3), 2000, pp. 292-295
Authors:
Chavanas, S
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Bodemer, C
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Hamel-Teillac, D
Wilkinson, J
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Leigh, IM
Harper, JI
Taieb, A
de Prost, Y
Cardon, LR
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Citation: S. Chavanas et al., Localization of the Netherton syndrome gene to chromosome 5q32, by linkageanalysis and homozygosity mapping, AM J HU GEN, 66(3), 2000, pp. 914-921
Authors:
Bodemer, C
Amoric, JC
Hamel-Teillac, D
de Prost, Y
Citation: C. Bodemer et al., Localized scleroderma in childhood and therapeutic trial with calcitriol: a therapeutic option to define, ANN DER VEN, 126(10), 1999, pp. 725-726