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American Journal of Medical Genetics
|
March 10, 2000
Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome
A König, R Happle, D Bornholdt, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete
|
September 1, 1992
[Rhabdomyosarcoma: differential diagnosis of cutaneous tumors in childhood]
E B Bröcker, H Hamm, J Ritter, et al.
Dermatology (Basel, Switzerland)
|
September 6, 2000
New type of epidermal nevus syndrome
T Gobello, C Mazzanti, G Zambruno, et al.
American Journal of Medical Genetics
|
June 13, 1997
Paired melanotic and achromic macules in a case of phacomatosis pigmentovascularis: a further example of twin spotting?
E de las Heras, J P Boixeda, A Ledo, et al.
Annales De Dermatologie Et De Venereologie
|
August 1, 1980
[Congenital homolateral epidermal hyperplasia and hypoplastic hemidysplasia (splitting of the Solomon's syndrome) (author's transl)]
G Laplanche, E Grosshans, O Gabriel-Robez, et al.
Dermatology (Basel, Switzerland)
|
July 15, 2000
Multiple familial basal cell carcinomas including a case of segmental manifestation
B Guarneri, F Borgia, S P Cannavò, et al.
European Journal of Dermatology : EJD
|
March 22, 2000
Sweat testing in hypomelanosis of Ito: divergent results reflecting genetic heterogeneity
P M Steijlen, H E Viëtor, M V Steensel, et al.
Acta Dermato-Venereologica
|
January 1, 1981
Physiocochemical properties of "spun glass" hair
H P Baden, R J Schoenfeld, J D Stroud, et al.
Lymphology
|
December 1, 1979
Roentgenographic and clinical signs in yellow nail syndrome
R P Müller, P E Peters, K Echternacht-Happle, et al.
Acta Dermato-Venereologica
|
January 1, 1990
Elastase-inhibiting activity in scaling skin disorders
A Chang, J Schalkwijk, R Happle, et al.
Page
of 46
Search research articles
Search
Showing results (361-370 of 459) with videos related to
Sort By:
Page
of 46
American Journal of Medical Genetics
|
March 10, 2000
Mutations in the NSDHL gene, encoding a 3beta-hydroxysteroid dehydrogenase, cause CHILD syndrome
A König, R Happle, D Bornholdt, et al.
Der Hautarzt; Zeitschrift Fur Dermatologie, Venerologie, Und Verwandte Gebiete
|
September 1, 1992
[Rhabdomyosarcoma: differential diagnosis of cutaneous tumors in childhood]
E B Bröcker, H Hamm, J Ritter, et al.
Dermatology (Basel, Switzerland)
|
September 6, 2000
New type of epidermal nevus syndrome
T Gobello, C Mazzanti, G Zambruno, et al.
American Journal of Medical Genetics
|
June 13, 1997
Paired melanotic and achromic macules in a case of phacomatosis pigmentovascularis: a further example of twin spotting?
E de las Heras, J P Boixeda, A Ledo, et al.
Annales De Dermatologie Et De Venereologie
|
August 1, 1980
[Congenital homolateral epidermal hyperplasia and hypoplastic hemidysplasia (splitting of the Solomon's syndrome) (author's transl)]
G Laplanche, E Grosshans, O Gabriel-Robez, et al.
Dermatology (Basel, Switzerland)
|
July 15, 2000
Multiple familial basal cell carcinomas including a case of segmental manifestation
B Guarneri, F Borgia, S P Cannavò, et al.
European Journal of Dermatology : EJD
|
March 22, 2000
Sweat testing in hypomelanosis of Ito: divergent results reflecting genetic heterogeneity
P M Steijlen, H E Viëtor, M V Steensel, et al.
Acta Dermato-Venereologica
|
January 1, 1981
Physiocochemical properties of "spun glass" hair
H P Baden, R J Schoenfeld, J D Stroud, et al.
Lymphology
|
December 1, 1979
Roentgenographic and clinical signs in yellow nail syndrome
R P Müller, P E Peters, K Echternacht-Happle, et al.
Acta Dermato-Venereologica
|
January 1, 1990
Elastase-inhibiting activity in scaling skin disorders
A Chang, J Schalkwijk, R Happle, et al.
Page
of 46