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Archives of Disease in Childhood. Fetal and Neonatal Edition|July 1, 1994
A new peroxisomal disorder with fetal and neonatal adrenal insufficiencyC Vanhole, F de Zegher, P Casaer, et al.Genetic Counseling (Geneva, Switzerland)|April 7, 1999
The phenotypic spectrum of the 10p deletion syndrome versus the classical DiGeorge syndromeH Van Esch, P Groenen, J P Fryns, et al.Acta Oto-Rhino-Laryngologica Belgica|March 21, 2001
Clinical features in 130 patients with the velo-cardio-facial syndrome. The Leuven experienceG Vantrappen, N Rommel, K Devriendt, et al.Genetic Counseling (Geneva, Switzerland)|November 15, 2006
Mathematical disabilities in young primary school children with velo-cardio-facial syndromeB De Smedt, A Swillen, K Devriendt, et al.European Journal of Obstetrics, Gynecology, and Reproductive Biology|April 21, 1992
Subcapsular hemorrhage of the liver and hemoperitoneum in premature infants: report of 4 casesF Emma, J Smith, P H Moerman, et al.Clinical Nutrition (Edinburgh, Scotland)|October 1, 1993
Standard two-compartment formulation for total parenteral nutrition in the neonatal intensive care unit: A fluid tolerance based systemH Devlieger, L De Pourcq, A Casneuf, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1996
Non-immune hydrops fetalis caused by beta-glucuronidase deficiency (mucopolysaccharidosis VII). Study of a family with 3 affected siblingsJ Van Dorpe, P Moerman, A Pecceu, et al.American Journal of Medical Genetics|December 1, 1990
Opitz C syndrome and pseudohypoaldosteronismJ De Koster, E Legius, F de Zegher, et al.American Journal of Medical Genetics|March 1, 1990
Pathogenesis of the lethal multiple pterygium syndromeP Moerman, J P Fryns, A Cornelis, et al.Biology of the Neonate|January 1, 1991
Different patterns of pulmonary sequelae after hyaline membrane disease: heterogeneity of bronchopulmonary dysplasia? A clinicopathologic studyS Van Lierde, A Cornelis, H Devlieger, et al.Pageof 105