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P M Steijlen

Showing results (141-150 of 145) with videos related to

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Archives of Dermatology|June 2, 1998
Restrictive dermopathy. Report of 12 cases. Dutch Task Force on GenodermatologyJ H Smitt, C J van Asperen, C M Niessen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 17, 2023
Expanding the molecular and clinical spectrum of autosomal recessive congenital ichthyosis caused by pathogenic variants in NIPAL4 and PNPLA1 and evaluation of novel therapeutic interventionsS V J Rossel, J M K Clabbers, P M Steijlen, et al.
The British Journal of Dermatology|September 24, 2016
Postzygotic mosaicism in basal cell naevus syndromeM G H C Reinders, H J Boersma, E M Leter, et al.
American Journal of Human Genetics|July 27, 1999
The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencingM van Steensel, F J Smith, P M Steijlen, et al.
Human Molecular Genetics|August 11, 1999
ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation classV L Ruiz-Perez, S A Carter, E Healy, et al.
Pageof 15

Showing results (141-150 of 145) with videos related to

Sort By:
Pageof 15
You have reached the last page of results.This site can display upto 145 results.
Archives of Dermatology|June 2, 1998
Restrictive dermopathy. Report of 12 cases. Dutch Task Force on GenodermatologyJ H Smitt, C J van Asperen, C M Niessen, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV|July 17, 2023
Expanding the molecular and clinical spectrum of autosomal recessive congenital ichthyosis caused by pathogenic variants in NIPAL4 and PNPLA1 and evaluation of novel therapeutic interventionsS V J Rossel, J M K Clabbers, P M Steijlen, et al.
The British Journal of Dermatology|September 24, 2016
Postzygotic mosaicism in basal cell naevus syndromeM G H C Reinders, H J Boersma, E M Leter, et al.
American Journal of Human Genetics|July 27, 1999
The gene for hypotrichosis of Marie Unna maps between D8S258 and D8S298: exclusion of the hr gene by cDNA and genomic sequencingM van Steensel, F J Smith, P M Steijlen, et al.
Human Molecular Genetics|August 11, 1999
ATP2A2 mutations in Darier's disease: variant cutaneous phenotypes are associated with missense mutations, but neuropsychiatric features are independent of mutation classV L Ruiz-Perez, S A Carter, E Healy, et al.
Pageof 15