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The Journal of Pediatrics|April 11, 2001
Prevalence of 22q11 deletion in fetuses with conotruncal cardiac defects: a 6-year prospective studyY Boudjemline, L Fermont, J Le Bidois, et al.Heart (British Cardiac Society)|August 24, 2000
Mechanical properties of the common carotid artery in Williams syndromeY Aggoun, D Sidi, B I Levy, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|May 1, 1995
[Gene localisation in 12q12 in Holt-Oram atrio-digital syndrome]D Bonnet, J Terrett, E Pequignot-Viegas, et al.Journal De Genetique Humaine|January 1, 1989
[Stature after 18 months of treatment with synthetic growth hormone in 12 patients with Turner's syndrome]B Leheup, M PiersonAmerican Journal of Medical Genetics|January 20, 1997
Microsatellite DNA markers detects 95% of chromosome 22q11 deletionsD Bonnet, V Cormier-Daire, J Kachaner, et al.Acta Paediatrica (Oslo, Norway : 1992)|June 26, 1998
Three-year data from a comparative study with recombinant human growth hormone in the treatment of short stature in young children with intrauterine growth retardationA Fjellestad-Paulsen, P Czernichow, R Brauner, et al.Heart (British Cardiac Society)|April 16, 1998
Relation of genotype 22q11 deletion to phenotype of pulmonary vessels in tetralogy of Fallot and pulmonary atresia-ventricular septal defectM Chessa, G Butera, P Bonhoeffer, et al.Acta Paediatrica Scandinavica|March 1, 1976
Evaluation of single oral dose metyrapone tests in children with hypopituitarismJ M Limal, A Basmaciogullari, R RappaportPageof 59