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Results: 1-10 |
Results: 10
Hypotrichosis, lymphedema of the legs and acral telangiectasias - new syndrome?
Authors: Glade, C van Steensel, MAM Steijlen, PM
Citation: C. Glade et al., Hypotrichosis, lymphedema of the legs and acral telangiectasias - new syndrome?, EUR J DERM, 11(6), 2001, pp. 515-517
The molecular basis of hair growth
Authors: van Steensel, MAM van Geel, M Steijlen, PM
Citation: Mam. Van Steensel et al., The molecular basis of hair growth, EUR J DERM, 11(4), 2001, pp. 348-352
A new type of pachyonychia congenita
Authors: van Steensel, MAM Smith, FJD Steijlen, PM
Citation: Mam. Van Steensel et al., A new type of pachyonychia congenita, EUR J DERM, 11(3), 2001, pp. 188-190
Familial occurrence of nevus sebaceus of Jadassohn: another case of paradominant inheritance?
Authors: Laino, L van Steensel, MAM Innocenzi, D Camplone, G
Citation: L. Laino et al., Familial occurrence of nevus sebaceus of Jadassohn: another case of paradominant inheritance?, EUR J DERM, 11(2), 2001, pp. 97-98
Woolly hair, premature loss of teeth, nail dystrophy, acral hyperkeratosisand facial abnormalities: possible new syndrome in a Dutch kindred
Authors: van Steensel, MAM Koedam, MI Swinkels, OQ Rietveld, F Steijlen, PM
Citation: Mam. Van Steensel et al., Woolly hair, premature loss of teeth, nail dystrophy, acral hyperkeratosisand facial abnormalities: possible new syndrome in a Dutch kindred, BR J DERM, 145(1), 2001, pp. 157-161
Sweat testing in hypomelanosis of Ito: divergent results reflecting genetic heterogeneity
Authors: Steijlen, PM Vietor, HE van Steensel, MAM Happle, R
Citation: Pm. Steijlen et al., Sweat testing in hypomelanosis of Ito: divergent results reflecting genetic heterogeneity, EUR J DERM, 10(3), 2000, pp. 217-219
Molecular genetics of the hair follicle: The state of the art
Authors: van Steensel, MAM Happle, R Steijlen, PM
Citation: Mam. Van Steensel et al., Molecular genetics of the hair follicle: The state of the art, P SOC EXP M, 223(1), 2000, pp. 1-7
Probing the Gene eXpression Database for candidate genes
Authors: van Steensel, MAM Celli, J van Bokhoven, JH Brunner, HG
Citation: Mam. Van Steensel et al., Probing the Gene eXpression Database for candidate genes, EUR J HUM G, 7(8), 1999, pp. 910-919
Paradominant inheritance, a hypothesis explaining occasional familial occurrence of sporadic syndromes
Authors: Steijlen, PM van Steensel, MAM
Citation: Pm. Steijlen et Mam. Van Steensel, Paradominant inheritance, a hypothesis explaining occasional familial occurrence of sporadic syndromes, AM J MED G, 85(4), 1999, pp. 359-360
Hypomelanosis of Ito: A symptom, not a syndrome
Authors: van Steensel, MAM Steijlen, PM
Citation: Mam. Van Steensel et Pm. Steijlen, Hypomelanosis of Ito: A symptom, not a syndrome, AM J MED G, 80(4), 1998, pp. 435-435
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