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Nature Genetics|October 19, 2004
Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosisJan Hellemans, Olena Preobrazhenska, Andy Willaert, et al.
Calcified Tissue International|March 14, 2025
Loss of the Ubiquitin-Associated Domain of sqstm1/p62 in Zebrafish Causes a Phenotype Resembling Paget's Disease of BoneYentl Huybrechts, Raphaël De Ridder, Dylan Bergen, et al.
Comparative Biochemistry and Physiology. Part A, Molecular & Integrative Physiology|May 19, 2026
In vivo PET imaging of zebrafish and its application for detecting metabolic changes in response to lipopolysaccharideLuiza Reali Nazario, Guilherme Pietro da Silva, Jéssica Streb de Sousa, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 19, 2014
Refinement of the critical 2p25.3 deletion region: the role of MYT1L in intellectual disability and obesityNina De Rocker, Sarah Vergult, David Koolen, et al.
Cell|January 12, 2022
Spatial proteogenomics reveals distinct and evolutionarily conserved hepatic macrophage nichesMartin Guilliams, Johnny Bonnardel, Birthe Haest, et al.
American Journal of Human Genetics|April 15, 2014
Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problemsAnneke T Vulto-van Silfhout, Shivakumar Rajamanickam, Philip J Jensik, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 12, 2018
Arterial tortuosity syndrome: 40 new families and literature reviewAude Beyens, Juliette Albuisson, Annekatrien Boel, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 12, 2018
Correction: Arterial tortuosity syndrome: 40 new families and literature reviewAude Beyens, Juliette Albuisson, Annekatrien Boel, et al.
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