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Clinical Dysmorphology|May 13, 1999
Robinow syndrome in monozygotic twins with normal statureJ M Saraiva, I Cordeiro, H G SantosRevista De Neurologia|March 28, 2008
[Simultaneous occurrence of neurofibromatosis and tuberous sclerosis, acquired as neo-mutations]P C Janeiro, M S Cunha, I Cordeiro, et al.Bulletin of Environmental Contamination and Toxicology|April 9, 2021
Short-Term Effects of Wildfire Ash on Water Quality Parameters: A Laboratory ApproachDarlan Q Brito, Luiz H G Santos, Carlos José Sousa Passos, et al.American Journal of Human Genetics|February 11, 1999
Brachydactyly type B: linkage to chromosome 9q22 and evidence for genetic heterogeneityM Oldridge, I K Temple, H G Santos, et al.Clinical Genetics|February 14, 2009
Clinical and molecular diagnosis of the skeletal dysplasias associated with mutations in the gene encoding Fibroblast Growth Factor Receptor 3 (FGFR3) in PortugalM R Almeida, A B Campos-Xavier, A Medeira, et al.European Journal of Pediatrics|February 1, 2000
Manifestations and treatment of Schimke immuno-osseous dysplasia: 14 new cases and a review of the literatureC F Boerkoel, S O'Neill, J L André, et al.Clinical Genetics|January 17, 2013
MLL2 mutation detection in 86 patients with Kabuki syndrome: a genotype-phenotype studyP Makrythanasis, B W van Bon, M Steehouwer, et al.Pageof 1