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American Journal of Human Genetics|August 5, 2005
Genomewide linkage study in 1,176 affected sister pair families identifies a significant susceptibility locus for endometriosis on chromosome 10q26Susan A Treloar, Jacqueline Wicks, Dale R Nyholt, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 6, 2022
Alpelisib for the treatment of PIK3CA-related head and neck lymphatic malformations and overgrowthTara L Wenger, Sheila Ganti, Catherine Bull, et al.Journal of Interventional Cardiac Electrophysiology : an International Journal of Arrhythmias and Pacing|June 23, 2022
Randomized trial of conventional versus radiofrequency needle transseptal puncture for cryoballoon ablation: the CRYO-LATS trialJason G Andrade, Laurent Macle, Matthew T Bennett, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 14, 2026
Mutations in VCP cause Adams-Oliver syndrome with or without pulmonary hypertensionAnna Lehman, Sana Ahmed, Arezoo Mohajeri, et al.ACS Central Science|April 3, 2019
Large-Scale Production of 119mTe and 119Sb for Radiopharmaceutical ApplicationsKevin T Bennett, Sharon E Bone, Andrew C Akin, et al.Biorxiv : the Preprint Server for Biology|April 27, 2026
Long-read MitoScope reveals tissue-resolved somatic mitochondrial variation and landscape of nuclear-embedded mitochondrial sequencesChristina Zakarian, Joshua D Smith, Chee Hong Wong, et al.BMJ Open|March 25, 2022
Association of the Intermountain Risk Score with major adverse health events in patients positive for COVID-19: an observational evaluation of a US cohortBenjamin D Horne, Joseph R Bledsoe, Joseph B Muhlestein, et al.American Journal of Human Genetics|April 16, 2019
Homozygous Mutations in CSF1R Cause a Pediatric-Onset Leukoencephalopathy and Can Result in Congenital Absence of MicrogliaNynke Oosterhof, Irene J Chang, Ehsan Ghayoor Karimiani, et al.Journal of Medical Genetics|January 4, 2014
Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic herniaLan Yu, James T Bennett, Julia Wynn, et al.Journal of Medical Genetics|June 9, 2017
Loss of function in ROBO1 is associated with tetralogy of Fallot and septal defectsPaul Kruszka, Pranoot Tanpaiboon, Katherine Neas, et al.Pageof 74