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Archives of Dermatology|July 13, 2000
Cutaneous involvement in patients with angioimmunoblastic lymphadenopathy with dysproteinemia: a clinical, immunohistological, and molecular analysisP Martel, L Laroche, P Courville, et al.Annales De Chirurgie|January 1, 1996
[Genetics of Hirschsprung disease]T Attié, J Amiel, D Jan, et al.Journal of Medical Genetics|October 1, 1992
The gene for hereditary multiple exostoses does not map to the Langer-Giedion region (8q23-q24)M Le Merrer, K Ben Othmane, V Stanescu, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 28, 2017
[Acute hemorrhagic edema of infancy associated with Coxsackie virus infection]A Debray, V Ollier, A Coutard, et al.American Journal of Medical Genetics|May 22, 1995
Craniosynostosis and kidney malformation in a case of Hennekam syndromeV Cormier-Daire, S Lyonnet, A Lehnert, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 1, 1996
[Pregnancy and the child of a mother with phenylketonuria]V Abadie, E Depondt, J P Farriaux, et al.The British Journal of Dermatology|August 1, 1994
Disseminated superficial porokeratosis in a patient with AIDSJ Kanitakis, L Misery, J F Nicolas, et al.Clinical Genetics|April 14, 2015
A review of craniofacial disorders caused by spliceosomal defectsD Lehalle, D Wieczorek, R M Zechi-Ceide, et al.The British Journal of Dermatology|September 15, 2018
Management of congenital ichthyoses: European guidelines of care, part oneJ Mazereeuw-Hautier, A Vahlquist, H Traupe, et al.The British Journal of Dermatology|June 14, 2018
Management of congenital ichthyoses: European guidelines of care, part twoJ Mazereeuw-Hautier, A Hernández-Martín, E A O'Toole, et al.Pageof 38