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Reproductive Health|July 5, 2013
Feasibility and safety study of a new device (Odón device) for assisted vaginal deliveries: study protocol, Javier A Schvartzman, Hugo Krupitzki, et al.
HGG Advances|April 5, 2021
The PAX1 locus at 20p11 is a potential genetic modifier for bilateral cleft lipSarah W Curtis, Daniel Chang, Myoung Keun Lee, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|January 17, 2025
Familial Oculoauriculovertebral Spectrum: A Genomic Investigation of Autosomal Dominant InheritanceAline L Petrin, Ligiane Alves Machado-Paula, Austin Hinkle, et al.
American Journal of Human Genetics|May 10, 2011
Whole-Exome sequencing identifies FAM20A mutations as a cause of amelogenesis imperfecta and gingival hyperplasia syndromeJames O'Sullivan, Carolina C Bitu, Sarah B Daly, et al.
The Journal of Pediatrics|January 18, 2013
Late-onset sepsis in very low birth weight infants from singleton and multiple-gestation birthsNansi S Boghossian, Grier P Page, Edward F Bell, et al.
American Journal of Medical Genetics. Part A|May 17, 2011
Genomic strategy identifies a missense mutation in WD-repeat domain 65 (WDR65) in an individual with Van der Woude syndromeNicholas K Rorick, Akira Kinoshita, Jason L Weirather, et al.
BMC Public Health|February 16, 2024
Perceptions and beliefs of community gatekeepers about genomic risk information in African cleft researchAbimbola M Oladayo, Oluwakemi Odukoya, Veronica Sule, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|December 7, 2018
Genetic variants associated with patent ductus arteriosus in extremely preterm infantsJohn M Dagle, Kelli K Ryckman, Cassandra N Spracklen, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|January 24, 2022
Targeted newborn metabolomics: prediction of gestational age from cord bloodElizabeth A Jasper, Scott P Oltman, Elizabeth E Rogers, et al.
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