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Orthodontics & Craniofacial Research|July 27, 2007
Genetic analysis of non-syndromic craniosynostosisS A Boyadjiev, Clinical Genetics|June 14, 2000
Online Mendelian Inheritance in Man (OMIM) as a knowledgebase for human developmental disordersS A Boyadjiev, E W JabsJournal of Inherited Metabolic Disease|May 9, 2000
Three cases of intravenous sodium benzoate and sodium phenylacetate toxicity occurring in the treatment of acute hyperammonaemiaV Praphanphoj, S A Boyadjiev, L J Waber, et al.Journal of Medical Genetics|September 11, 1998
Familial craniosynostosis, anal anomalies, and porokeratosis: CAP syndromeN Flanagan, S A Boyadjiev, J Harper, et al.Journal of Inherited Metabolic Disease|July 23, 2003
The relationship of plasma glutamine to ammonium and of glycine to acid-base balance in propionic acidaemiaZ N Al-Hassnan, S A Boyadjiev, V Praphanphoj, et al.Cancer Research|March 15, 1997
High frequency in vivo loss of heterozygosity is primarily a consequence of mitotic recombinationP K Gupta, A Sahota, S A Boyadjiev, et al.American Journal of Human Genetics|March 11, 2000
Paternal origin of FGFR2 mutations in sporadic cases of Crouzon syndrome and Pfeiffer syndromeR L Glaser, W Jiang, S A Boyadjiev, et al.Cytogenetic and Genome Research|February 14, 2003
Physical map of the chromosome 6q22 region containing the oculodentodigital dysplasia locus: analysis of thirteen candidate genes and identification of novel ESTs and DNA polymorphismsS A Boyadjiev, A B Chowdry, R E Shapiro, et al.The Journal of Urology|February 26, 2008
Epidemiological survey of 214 families with bladder exstrophy-epispadias complexL Gambhir, T Höller, M Müller, et al.Clinical Genetics|April 29, 2005
Molecular screening for microdeletions at 9p22-p24 and 11q23-q24 in a large cohort of patients with trigonocephalyF S Jehee, D Johnson, L G Alonso, et al.Pageof 2