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The Laryngoscope|September 5, 2020
Genotype-Phenotype Correlation of Tracheal Cartilaginous Sleeves and Fgfr2 Mutations in MiceAustin S Lam, Carrie C Liu, Gail H Deutsch, et al.
American Journal of Medical Genetics. Part A|August 6, 2013
Further characterization of atypical features in auriculocondylar syndrome caused by recessive PLCB4 mutationsYasuhiro Kido, Christopher T Gordon, Satoru Sakazume, et al.
Critical Reviews in Toxicology|November 5, 2013
Mode of action framework analysis for receptor-mediated toxicity: The peroxisome proliferator-activated receptor alpha (PPARα) as a case studyJ Christopher Corton, Michael L Cunningham, B Timothy Hummer, et al.
Journal of Neurosurgery. Pediatrics|June 21, 2024
AXIN1 mutations in nonsyndromic craniosynostosisAndrew T Timberlake, Kshipra Hemal, Jonas A Gustafson, et al.
Disease Models & Mechanisms|March 14, 2022
Auriculocondylar syndrome 2 results from the dominant-negative action of PLCB4 variantsStanley M Kanai, Caleb Heffner, Timothy C Cox, et al.
Pediatric Radiology|July 25, 2003
Ultrasound screening of the lambdoid suture in the child with posterior plagiocephalyRaymond W Sze, Marguerite T Parisi, Manrita Sidhu, et al.
American Journal of Medical Genetics. Part A|October 14, 2005
Skeletal changes in epidermal nevus syndrome: does focal bone disease harbor clues concerning pathogenesis?Carrie L Heike, Michael L Cunningham, Robert D Steiner, et al.
Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|September 28, 2007
Memory and response inhibition in young children with single-suture craniosynostosisKaren Toth, Brent Collett, Kathleen A Kapp-Simon, et al.
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