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European Journal of Human Genetics : EJHG|June 15, 2000
Linkage of Marie-Unna hypotrichosis locus to chromosome 8p21 and exclusion of 10 genes including the hairless gene by mutation analysisP Lefevre, A Rochat, C Bodemer, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 29, 2001
[Evaluation of 47,213 infants in neonatal screening for cystic fibrosis, using pancreatitis-associated protein and immunoreactive trypsinogen assays]S Barthellemy, N Maurin, M Roussey, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|December 3, 2014
[Uncommon neonatal case of hypoglycemia: ACTH resistance syndrome]O Delmas, C Marrec, E Caietta, et al.
Neuro-Chirurgie|January 1, 1988
[Recurrent intracranial hematomas disclosing Rendu-Osler disease in a pregnant woman]J P Neau, G Roualdes, B Bataille, et al.
European Journal of Clinical Microbiology & Infectious Diseases : Official Publication of the European Society of Clinical Microbiology|May 19, 2009
Microbial diversity in the sputum of a cystic fibrosis patient studied with 16S rDNA pyrosequencingF Armougom, F Bittar, N Stremler, et al.
La Revue De Medecine Interne|June 14, 2001
[Thymoma and disseminated lupus erythematosus. Two new cases and review of the literature]I Genty, R Jean, E Cretel, et al.
Journal of Inherited Metabolic Disease|January 25, 2008
NTBC treatment in tyrosinaemia type I: long-term outcome in French patientsA Masurel-Paulet, J Poggi-Bach, M-O Rolland, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|February 1, 1994
[Antigliadin, antireticulin, antiendomysium antibodies: value in the diagnosis and follow-up of celiac disease in children]J P Olives, J J Baudon, A Dabadie, et al.
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