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Brain & Development
|
January 1, 1980
Tuberous sclerosis: the incidence of sporadic cases versus familial cases
P Fleury, W P de Groot, J W Delleman, et al.
British Medical Journal (Clinical Research Ed.)
|
January 21, 1984
Recognising placental steroid sulphatase deficiency
A 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 ichthyosis
A 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 deficiency
W 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 VIIB
F 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 parameters
N 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 observations
A 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 mutation
D 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 cases
P Fleury, K Dingemans, W P de Groot, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 29) with videos related to
Sort By:
Page
of 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 cases
P Fleury, W P de Groot, J W Delleman, et al.
British Medical Journal (Clinical Research Ed.)
|
January 21, 1984
Recognising placental steroid sulphatase deficiency
A 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 ichthyosis
A 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 deficiency
W 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 VIIB
F 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 parameters
N 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 observations
A 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 mutation
D 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 cases
P Fleury, K Dingemans, W P de Groot, et al.
Page
of 3