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American Journal of Medical Genetics. Part A|April 29, 2020
Eye tracking as an objective measure of hyperphagia in children with Prader-Willi syndromeAlexandra P Key, Hatun Zengin-Bolatkale, Anastasia Dimitropoulos, et al.American Journal of Medical Genetics. Part A|June 2, 2020
Pathogenic variants in EP300 and ANKRD11 in patients with phenotypes overlapping Cornelia de Lange syndromeFrancesco Cucco, Patrizia Sarogni, Sara Rossato, et al.American Journal of Medical Genetics. Part A|June 8, 2020
Baraitser-Winter cerebrofrontofacial syndrome: Report of two adult siblingsKarly Hampshire, Pierre-Marie Martin, Colleen Carlston, et al.American Journal of Medical Genetics. Part A|August 31, 2021
Victor Almon McKusick: In the footsteps of Mendel and OslerClair A FrancomanoAmerican Journal of Medical Genetics. Part A|September 8, 2021
Gain in growth after surgical repair of congenital heart disease among children with Down syndromeNazmus Saquib, Anas Naser Al Sarraj, Baraa Tarek Ziad Oubaied, et al.American Journal of Medical Genetics. Part A|September 16, 2021
Digital vascular lesions detected by transilluminationReed E PyeritzAmerican Journal of Medical Genetics. Part A|August 18, 2021
Clan genomics: From OMIM phenotypic traits to genes and biologyJames R LupskiAmerican Journal of Medical Genetics. Part A|September 15, 2021
Genetic and phenotypic heterogeneity in KIAA0753-related ciliopathiesKatherine A Inskeep, Yuri A Zarate, Danielle Monteil, et al.American Journal of Medical Genetics. Part A|October 27, 2019
Expanding the phenotype in Adams-Oliver syndrome correlating with the genotypeBenjamin Dudoignon, Celine Huber, Caroline Michot, et al.American Journal of Medical Genetics. Part A|April 8, 2020
Hip displacement in Wolf-Hirschhorn syndrome: Report on three cases and review of associated musculoskeletal pathologiesPranai K Buddhdev, Ataf Sabir, Michailis Kokkinakis, et al.Pageof 928