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American Journal of Human Genetics|December 1, 1996
Closing in on the Rieger syndrome gene on 4q25: mapping translocation breakpoints within a 50-kb regionN A Datson, E Semina, A A van Staalduinen, et al.American Journal of Medical Genetics. Part A|March 17, 2007
A genome-wide linkage scan for cleft lip and cleft palate identifies a novel locus on 8p11-23B M Riley, R E Schultz, M E Cooper, et al.American Journal of Human Genetics|December 1, 1996
Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locusE V Semina, N A Datson, N J Leysens, et al.Genomics|February 15, 1996
Development of a screening set for new (CAG/CTG)n dynamic mutationsJ M Gastier, T Brody, J C Pulido, et al.Nature Genetics|December 1, 1996
Cloning and characterization of a novel bicoid-related homeobox transcription factor gene, RIEG, involved in Rieger syndromeE V Semina, R Reiter, N J Leysens, et al.Journal of Dental Research|June 30, 2017
A Population-Based Study of Effects of Genetic Loci on Orofacial CleftsL M Moreno Uribe, T Fomina, R G Munger, et al.Molecular Genetics and Genomics : MGG|June 23, 2026
Genetic-epigenetic interactions (meQTLs) in orofacial clefts etiologyA L Petrin, L A Machado-Paula, H L Keen, et al.American Journal of Human Genetics|July 31, 1998
Association of MSX1 and TGFB3 with nonsyndromic clefting in humansA C Lidral, P A Romitti, A M Basart, et al.Medrxiv : the Preprint Server for Health Sciences|February 24, 2025
Genetic-epigenetic interactions (meQTLs) in orofacial clefts etiologyL A Machado-Paula, J Romanowska, R T Lie, et al.Genomics|February 15, 1996
Chromosomal assignment of 2900 tri- and tetranucleotide repeat markers using NIGMS somatic cell hybrid panel 2S L Sunden, T Businga, J Beck, et al.Pageof 32