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American Journal of Medical Genetics|March 21, 1998
Complete absence or deficiency of one half of the bodyA Carranza, E Gilbert-Barness, F Madrigal, et al.Pediatric Pathology|May 1, 1992
Pulmonary hypertension with coexisting portal hypertensionS O Rossi, E Gilbert-Barness, T Saari, et al.Pediatric Pathology|July 1, 1991
Isolated pulmonary Goodpasture syndromeP Harrity, E Gilbert-Barness, A Cabalka, et al.American Journal of Medical Genetics|August 3, 2001
Megacystis-microcolon-intestinal hypoperistalsis syndrome and aganglionosis in trisomy 18G Chamyan, D Debich-Spicer, J M Opitz, et al.Fetal and Pediatric Pathology|August 13, 2005
Tuberous sclerosis: immunohistochemistry expression of tuberin and hamartin in a 31-week gestational fetusM Vinaitheerthan, J Wei, M Mizuguchi, et al.Pediatric Neurology|April 1, 1995
Infantile progressive striato-thalamic degeneration in two siblings: a new syndromeM A Gieron, E Gilbert-Barness, J P Vonsattel, et al.American Journal of Medical Genetics|July 27, 2001
Evidence for the "midline" hypothesis in associated defects of laterality formation and multiple midline anomaliesE Gilbert-Barness, D Debich-Spicer, M M Cohen, et al.Journal of Diabetes and Its Complications|August 4, 1999
Diabetic cardiomyopathy and carnitine deficiencyJ I Malone, D D Schocken, A D Morrison, et al.American Journal of Medical Genetics|June 22, 2000
Ocular manifestations in Proteus syndromeI De Becker, D J Gajda, E Gilbert-Barness, et al.Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|February 9, 1999
Seckel-like syndrome in three siblingsS R Arnold, D Spicer, B Kouseff, et al.Pageof 5