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Pediatric Endocrinology Reviews : PER|June 28, 2019
Hormones and their Structural and Functional Effects on the Brain: How Can We Change our Practice Moving Forward?Bonnie McCann-Crosby, Laurel Hyle, David Mann, et al.Molecular Genetics and Metabolism|April 17, 2017
Elucidation of the complex metabolic profile of cerebrospinal fluid using an untargeted biochemical profiling assayAdam D Kennedy, Kirk L Pappan, Taraka R Donti, et al.Nature Genetics|June 5, 2007
Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasiaXiaoling Wang, V Reid Sutton, J Omar Peraza-Llanes, et al.JBMR Plus|October 5, 2018
Whole-Exome Sequencing Identifies an Intronic Cryptic Splice Site in <i>SERPINF1</i> Causing Osteogenesis Imperfecta Type VIZixue Jin, Lindsay C Burrage, Ming-Ming Jiang, et al.Pediatric Endocrinology Reviews : PER|July 18, 2015
Androgen Insensitivity Syndrome: Management Considerations from Infancy to AdulthoodMin-Jye Chen, Bach-Mai K Vu, Marni Axelrad, et al.International Journal of Pediatric Endocrinology|April 16, 2014
State of the art review in gonadal dysgenesis: challenges in diagnosis and managementBonnie McCann-Crosby, Roshanak Mansouri, Jennifer E Dietrich, et al.American Journal of Medical Genetics. Part A|August 3, 2016
SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset featuresPatricia G Wheeler, Bobby G Ng, Laura Sanford, et al.American Journal of Medical Genetics. Part A|June 15, 2023
A qualitative exploration of patient perspectives on psychosocial burdens and positive factors in adults with osteogenesis imperfectaW Conor Rork, Alyssa G Hertz, Andrew D Wiese, et al.International Journal of Pediatric Endocrinology|October 29, 2010
Consensus in Guidelines for Evaluation of DSD by the Texas Children's Hospital Multidisciplinary Gender Medicine TeamGanka Douglas, Marni E Axelrad, Mary L Brandt, et al.Molecular Genetics and Metabolism Reports|June 20, 2017
A non-mosaic <i>PORCN</i> mutation in a male with severe congenital anomalies overlapping focal dermal hypoplasiaSimran Madan, Wei Liu, James T Lu, et al.Pageof 18