Showing results (1-10 of 10) with videos related to
Sort By:
Pageof 1
Acta Paediatrica Scandinavica|July 1, 1987
Hypothyroidism in children with filter paper TSH of 30 to 50 microU/ml at initial screening. Implication of the TSH cut-off point for recalling of infants at riskJ Leger, M Lemerrer, M L Briard, et al.Ophthalmic Genetics|January 3, 2001
SHORT syndrome: a case with high hyperopia and astigmatismS Bonnel, P Dureau, M LeMerrer, et al.American Journal of Medical Genetics|April 14, 1997
Idiopathic thrombocytopenic purpura in two mothers of children with DiGeorge sequence: a new component manifestation of deletion 22q11?A Lévy, G Michel, M Lemerrer, et al.Archives Francaises De Pediatrie|January 1, 1987
[Congenital or neonatal hypothyroidism with filter-paper levels of TSH less than 50 microU/ml. Conclusions on the detection strategy in France]J Léger, M Lemerrer, M L Briard, et al.Prenatal Diagnosis|April 1, 1995
Prenatal diagnosis of cleft lip at 11 menstrual weeks using embryoscopy in the van der Woude syndromeM Dommergues, M Lemerrer, G Couly, et al.Prenatal Diagnosis|February 1, 1994
Meckel-Gruber syndrome: prenatal diagnosis at 10 menstrual weeks using embryoscopyY Dumez, M Dommergues, M C Gubler, et al.Fetal Diagnosis and Therapy|December 23, 2000
Prenatal diagnosis of sporadic Apert syndrome: a sequential diagnostic approach combining three-dimensional computed tomography and molecular biologyD Mahieu-Caputo, P Sonigo, J Amiel, et al.American Journal of Medical Genetics|March 10, 2001
Mazabraud syndrome in two patients: clinical overlap with McCune-Albright syndromeL Faivre, A Nivelon-Chevallier, M L Kottler, et al.American Journal of Human Genetics|January 13, 2000
Fibrodysplasia ossificans progressiva, a heritable disorder of severe heterotopic ossification, maps to human chromosome 4q27-31G Feldman, M Li, S Martin, et al.American Journal of Medical Genetics|April 29, 1998
CHARGE syndrome: report of 47 cases and reviewA L Tellier, V Cormier-Daire, V Abadie, et al.Pageof 1