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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 29, 2010
Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome)John M Graham, Robin D Clark, John B Moeschler, et al.American Journal of Medical Genetics. Part A|June 25, 2004
MICRO syndrome: an entity distinct from COFS syndromeJohn M Graham, Raoul Hennekam, William B Dobyns, et al.Neurology. Genetics|April 12, 2016
Mutation in the sixth immunoglobulin domain of L1CAM is associated with migrational brain anomaliesChristine Shieh, Franklin Moser, John M Graham, et al.Molecular Genetics and Metabolism|April 13, 2016
Terminal microdeletions of 13q34 chromosome region in patients with intellectual disability: Delineation of an emerging new microdeletion syndromeEyal Reinstein, Meytal Liberman, Michal Feingold-Zadok, et al.Frontiers in Pharmacology|January 9, 2023
A KCNB1 gain of function variant causes developmental delay and speech apraxia but not seizuresEmma L Veale, Alessia Golluscio, Katheryn Grand, et al.American Journal of Medical Genetics. Part A|July 29, 2018
A case of severe TBCE-negative hypoparathyroidism-retardation-dysmorphism syndrome: Case report and literature reviewAnna Ryabets-Lienhard, Satja Issaranggoon Na Ayuthaya, John M Graham, et al.American Journal of Medical Genetics. Part A|January 7, 2009
Elements of morphology: standard terminology for the periorbital regionBryan D Hall, John M Graham, Suzanne B Cassidy, et al.Clinical Pediatrics|September 5, 2013
Advances in Hirschsprung disease genetics and treatment strategies: an update for the primary care pediatricianDeepika D'Cunha Burkardt, John M Graham, Scott S Short, et al.American Journal of Medical Genetics. Part A|April 4, 2003
van den Ende-Gupta syndrome of blepharophimosis, arachnodactyly, and congenital contractures: clinical delineation and recurrence in brothersDaniela N Schweitzer, Ralph S Lachman, Barry D Pressman, et al.Pageof 64