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W P de Groot

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Brain & Development|January 1, 1980
Tuberous sclerosis: the incidence of sporadic cases versus familial casesP Fleury, W P de Groot, J W Delleman, et al.
British Medical Journal (Clinical Research Ed.)|January 21, 1984
Recognising placental steroid sulphatase deficiencyA C Jöbsis, C M van der Loos, J M Walboomers, et al.
The British Journal of Dermatology|May 1, 1983
A new method for the determination of steroid sulphatase activity in leukocytes in X-linked recessive ichthyosisA C Jöbsis, W P De Groot, A E Meijer, et al.
The British Journal of Dermatology|July 1, 1980
Sex-linked ichthyosis and placental sulphatase C deficiencyW P de Groot, A C Jobsis, A Marinkovic-Ilsen, et al.
The British Journal of Dermatology|January 1, 1992
Clinical features of an affected father and daughter with Ehlers-Danlos syndrome type VIIBF M Pope, A C Nicholls, A Palan, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 1, 1980
Severe congenital skin defects in a newborn. Case report and relevance of several obstetrical parametersN J Leschot, P E Treffers, M J Becker-Bloemkolk, et al.
The American Journal of Pathology|May 1, 1980
X-linked ichthyosis and X-linked placental sulfatase deficiency: a disease entity. Histochemical observationsA C Jöbsis, W P De Groot, A J Tigges, et al.
Acta Dermato-Venereologica|June 23, 2004
Life-long course and molecular characterization of the original Dutch family with epidermolysis bullosa simplex with muscular dystrophy due to a homozygous novel plectin point mutationD Koss-Harnes, B Høyheim, M F Jonkman, et al.
Clinical Neurology and Neurosurgery|January 1, 1986
Ito's hypomelanosis (incontinentia pigmenti achromians). A review of four casesP Fleury, K Dingemans, W P de Groot, et al.
Pageof 3

Showing results (21-30 of 29) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 29 results.
Brain & Development|January 1, 1980
Tuberous sclerosis: the incidence of sporadic cases versus familial casesP Fleury, W P de Groot, J W Delleman, et al.
British Medical Journal (Clinical Research Ed.)|January 21, 1984
Recognising placental steroid sulphatase deficiencyA C Jöbsis, C M van der Loos, J M Walboomers, et al.
The British Journal of Dermatology|May 1, 1983
A new method for the determination of steroid sulphatase activity in leukocytes in X-linked recessive ichthyosisA C Jöbsis, W P De Groot, A E Meijer, et al.
The British Journal of Dermatology|July 1, 1980
Sex-linked ichthyosis and placental sulphatase C deficiencyW P de Groot, A C Jobsis, A Marinkovic-Ilsen, et al.
The British Journal of Dermatology|January 1, 1992
Clinical features of an affected father and daughter with Ehlers-Danlos syndrome type VIIBF M Pope, A C Nicholls, A Palan, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|July 1, 1980
Severe congenital skin defects in a newborn. Case report and relevance of several obstetrical parametersN J Leschot, P E Treffers, M J Becker-Bloemkolk, et al.
The American Journal of Pathology|May 1, 1980
X-linked ichthyosis and X-linked placental sulfatase deficiency: a disease entity. Histochemical observationsA C Jöbsis, W P De Groot, A J Tigges, et al.
Acta Dermato-Venereologica|June 23, 2004
Life-long course and molecular characterization of the original Dutch family with epidermolysis bullosa simplex with muscular dystrophy due to a homozygous novel plectin point mutationD Koss-Harnes, B Høyheim, M F Jonkman, et al.
Clinical Neurology and Neurosurgery|January 1, 1986
Ito's hypomelanosis (incontinentia pigmenti achromians). A review of four casesP Fleury, K Dingemans, W P de Groot, et al.
Pageof 3