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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|August 4, 2004
[Disseminated lupus erythematosus in children: guidelines about investigations during the initial evaluation and follow-up]B Bader-Meunier, E Haddad, P Niaudet, et al.Journal of Medical Genetics|July 15, 2006
Array-based comparative genomic hybridisation identifies high frequency of cryptic chromosomal rearrangements in patients with syndromic autism spectrum disordersM-L Jacquemont, D Sanlaville, R Redon, et al.Journal of Medical Genetics|April 16, 2002
Automated fluorescent genotyping detects 10% of cryptic subtelomeric rearrangements in idiopathic syndromic mental retardationM Rio, F Molinari, S Heuertz, et al.American Journal of Human Genetics|October 12, 2001
Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structuresJ Amiel, Y Espinosa-Parrilla, J Steffann, et al.Clinical Genetics|July 16, 2004
Genome-wide screening using automated fluorescent genotyping to detect cryptic cytogenetic abnormalities in children with idiopathic syndromic mental retardationG Borck, M Rio, D Sanlaville, et al.European Journal of Human Genetics : EJHG|May 30, 2001
A novel automated strategy for screening cryptic telomeric rearrangements in children with idiopathic mental retardationL Colleaux, M Rio, S Heuertz, et al.The Journal of Pediatrics|May 5, 2005
Initial presentation of childhood-onset systemic lupus erythematosus: a French multicenter studyB Bader-Meunier, J B Armengaud, E Haddad, et al.Rheumatology (Oxford, England)|June 15, 2000
Favourable outcome in 135 children with juvenile systemic sclerosis: results of a multi-national surveyI Foeldvari, M Zhavania, N Birdi, et al.Annals of the Rheumatic Diseases|September 14, 2004
Autologous stem cell transplantation for refractory juvenile idiopathic arthritis: analysis of clinical effects, mortality, and transplant related morbidityI M De Kleer, D M C Brinkman, A Ferster, et al.Annales De Genetique|January 1, 1997
Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children)M Mathieu, C Piussan, F Thepot, et al.Pageof 19