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The American Journal of Clinical Nutrition|August 12, 2008
Age-appropriate body mass index in children with achondroplasia: interpretation in relation to indexes of heightJulie E Hoover-Fong, Kerry J Schulze, John McGready, et al.Pediatric Neurology|October 2, 2007
Albinism and developmental delay: the need to test for 15q11-q13 deletionReem Saadeh, Emily C Lisi, Denise A S Batista, et al.Journal of Neurosurgery. Pediatrics|May 6, 2017
Endoscopic surgery for patients with syndromic craniosynostosis and the requirement for additional open surgeryDavid S Hersh, Julie E Hoover-Fong, Natalie Beck, et al.American Journal of Medical Genetics. Part A|January 24, 2019
Growth hormone deficiency, aortic dilation, and neurocognitive issues in Feingold syndrome 2Michael Muriello, Alexander Y Kim, Krista Sondergaard Schatz, et al.Journal of the Endocrine Society|March 5, 2026
Effect of vosoritide on spine morphology in children with achondroplasia: 1-year results from a randomized phase 2 studyMelita Irving, Ravi Savarirayan, Julie E Hoover-Fong, et al.Quality of Life Research : an International Journal of Quality of Life Aspects of Treatment, Care and Rehabilitation|November 21, 2016
Factors associated with health-related quality of life (HRQOL) in adults with short stature skeletal dysplasiasNitasha Dhiman, Alia Albaghdadi, Cheryl K Zogg, et al.American Journal of Medical Genetics. Part A|March 3, 2009
Molecular (SNP) analyses of overlapping hemizygous deletions of 10q25.3 to 10qter in four patients: evidence for HMX2 and HMX3 as candidate genes in hearing and vestibular functionNathaniel D Miller, Melonie A Nance, Elizabeth S Wohler, et al.American Journal of Medical Genetics. Part A|January 28, 2003
Facial dysgenesis: a novel facial syndrome with chromosome 7 deletion p15.1-21.1Julie E Hoover-Fong, J Cai, C B Cargile, et al.Genome Research|September 6, 2011
Characterization of complex chromosomal rearrangements by targeted capture and next-generation sequencingNara L M Sobreira, Veena Gnanakkan, Michael Walsh, et al.European Journal of Human Genetics : EJHG|September 9, 2010
Genomic analysis of partial 21q monosomies with variable phenotypesElisha D O Roberson, Elizabeth Squibb Wohler, Julie E Hoover-Fong, et al.Pageof 4