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American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 17, 2023
Genetic Markers Among the Israeli Druze Minority Population With End-Stage Kidney DiseaseOmer Shlomovitz, Danit Atias-Varon, Dina Yagel, et al.
American Journal of Medical Genetics. Part A|July 4, 2007
Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogeneticsSau W Cheung, Chad A Shaw, Daryl A Scott, et al.
Children'S Health Care : Journal of the Association for the Care of Children'S Health|August 26, 2025
Qualitative investigation of school experiences in children with osteogenesis imperfectaJulia M Morales, Andrew D Wiese, Whitney S Shepherd, et al.
Cell|April 19, 2016
Asprosin, a Fasting-Induced Glucogenic Protein HormoneChase Romere, Clemens Duerrschmid, Juan Bournat, et al.
Psychology & Health|October 10, 2025
Facilitators and barriers to care among individuals with osteogenesis imperfectaSelena Guo, Francesca C Gedeon, Andrew D Wiese, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 29, 2019
Mobility in osteogenesis imperfecta: a multicenter North American studyKaren M Kruger, Angela Caudill, Mercedes Rodriguez Celin, et al.
Cold Spring Harbor Molecular Case Studies|March 17, 2017
An exome sequencing study of Moebius syndrome including atypical cases reveals an individual with CFEOM3A and a TUBB3 mutationRonak M Patel, David Liu, Claudia Gonzaga-Jauregui, et al.
Nature Medicine|November 7, 2017
Asprosin is a centrally acting orexigenic hormoneClemens Duerrschmid, Yanlin He, Chunmei Wang, et al.
American Journal of Medical Genetics. Part A|February 13, 2023
Nosology of genetic skeletal disorders: 2023 revisionSheila Unger, Carlos R Ferreira, Geert R Mortier, et al.
European Journal of Human Genetics : EJHG|August 26, 2010
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairmentNicola Brunetti-Pierri, Alex R Paciorkowski, Roberto Ciccone, et al.
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