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Journal of the American Academy of Dermatology
|
May 1, 1994
Congenital atrichia, palmoplantar hyperkeratosis, mental retardation, and early loss of teeth in four siblings: a new syndrome?
P M Steijlen, H A Neumann, D J der Kinderen, et al.
Human Genetics
|
March 1, 1993
Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphism
H Traupe, U Vetter, R Happle, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
November 13, 2009
CHILD syndrome: the NSDHL gene and its role in CHILD syndrome, a rare hereditary disorder
G P Avgerinou, A P Asvesti, A D Katsambas, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 26, 2017
At first sight or second glance: clinical presentation of mosaic manifestations of autosomal dominant skin disorders - a case series
F Toberer, R Happle, R Schneiderbauer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 26, 2018
The PERIOPTER syndrome (periorificial and ptychotropic erythrokeratoderma): a new Mendelian disorder of cornification
A-C Bursztejn, R Happle, L Charbit, et al.
American Journal of Medical Genetics
|
December 1, 1992
False-negative prenatal diagnosis of restrictive dermopathy
B C Hamel, R Happle, P M Steylen, et al.
Archives of Dermatological Research
|
January 1, 1991
Expression of tenascin in perifollicular connective tissue: comparison of normal scalp and alopecia areata
H M van Baar, C M Perret, I M van Vlijmen-Willems, et al.
Archives of Dermatology
|
May 15, 1998
Phacomatosis pigmentokeratotica: report of new cases and further delineation of the syndrome
G Tadini, L Restano, R Gonzáles-Pérez, et al.
The British Journal of Dermatology
|
July 20, 2018
Mosaicism due to postzygotic mutations in women with focal dermal hypoplasia
L Heinz, E Bourrat, P Vabres, et al.
Acta Dermato-Venereologica
|
January 1, 1987
Substrate specific sulfatase activity from hair follicles in recessive X-linked ichthyosis
A C Dijkstra, A M Vermeesch-Markslag, E W Vromans, et al.
Page
of 46
Search research articles
Search
Showing results (441-450 of 459) with videos related to
Sort By:
Page
of 46
Journal of the American Academy of Dermatology
|
May 1, 1994
Congenital atrichia, palmoplantar hyperkeratosis, mental retardation, and early loss of teeth in four siblings: a new syndrome?
P M Steijlen, H A Neumann, D J der Kinderen, et al.
Human Genetics
|
March 1, 1993
Exclusion of the biglycan (BGN) gene as a candidate gene for the Happle syndrome, employing an intragenic single-strand conformational polymorphism
H Traupe, U Vetter, R Happle, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
November 13, 2009
CHILD syndrome: the NSDHL gene and its role in CHILD syndrome, a rare hereditary disorder
G P Avgerinou, A P Asvesti, A D Katsambas, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
March 26, 2017
At first sight or second glance: clinical presentation of mosaic manifestations of autosomal dominant skin disorders - a case series
F Toberer, R Happle, R Schneiderbauer, et al.
Journal of the European Academy of Dermatology and Venereology : JEADV
|
May 26, 2018
The PERIOPTER syndrome (periorificial and ptychotropic erythrokeratoderma): a new Mendelian disorder of cornification
A-C Bursztejn, R Happle, L Charbit, et al.
American Journal of Medical Genetics
|
December 1, 1992
False-negative prenatal diagnosis of restrictive dermopathy
B C Hamel, R Happle, P M Steylen, et al.
Archives of Dermatological Research
|
January 1, 1991
Expression of tenascin in perifollicular connective tissue: comparison of normal scalp and alopecia areata
H M van Baar, C M Perret, I M van Vlijmen-Willems, et al.
Archives of Dermatology
|
May 15, 1998
Phacomatosis pigmentokeratotica: report of new cases and further delineation of the syndrome
G Tadini, L Restano, R Gonzáles-Pérez, et al.
The British Journal of Dermatology
|
July 20, 2018
Mosaicism due to postzygotic mutations in women with focal dermal hypoplasia
L Heinz, E Bourrat, P Vabres, et al.
Acta Dermato-Venereologica
|
January 1, 1987
Substrate specific sulfatase activity from hair follicles in recessive X-linked ichthyosis
A C Dijkstra, A M Vermeesch-Markslag, E W Vromans, et al.
Page
of 46