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American Journal of Medical Genetics. Part A|February 18, 2021
Parent-authored memoirs: Lessons in the practice of narrative medicineJohn C CareyAmerican Journal of Medical Genetics. Part A|February 5, 2021
Long-term weight control in adults with Prader-Willi syndrome living in residential hostelsHarry J Hirsch, Fortu Benarroch, Larry Genstil, et al.American Journal of Medical Genetics. Part A|November 22, 2018
Atypical presentation of pediatric BRAF RASopathy with acute encephalopathyLidia Pezzani, Daniela Marchetti, Anna Cereda, et al.American Journal of Medical Genetics. Part A|February 11, 2021
Alazami syndrome: Report of three Indian patients with phenotypic spectrum from adolescence to adulthoodSweta Das, Koumudi Godbole, Suneetha Susan Cleave Abraham, et al.American Journal of Medical Genetics. Part A|January 14, 2021
Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotypeMaria Giovanna Tedesco, Fortunato Lonardo, Caterina Ceccarini, et al.American Journal of Medical Genetics. Part A|January 14, 2021
Evidence that FGFRL1 contributes to congenital diaphragmatic hernia development in humansYoel Gofin, Laura Palmer Mackay, Keren Machol, et al.American Journal of Medical Genetics. Part A|April 30, 2014
If not Angelman, what is it? A review of Angelman-like syndromesWen-Hann Tan, Lynne M Bird, Ronald L Thibert, et al.American Journal of Medical Genetics. Part A|February 8, 2017
Childhood cancer predisposition syndromes-A concise review and recommendations by the Cancer Predisposition Working Group of the Society for Pediatric Oncology and HematologyTim Ripperger, Stefan S Bielack, Arndt Borkhardt, et al.American Journal of Medical Genetics. Part A|February 10, 2017
Novel LINS1 missense mutation in a family with non-syndromic intellectual disabilityJayesh Sheth, Gyan Ranjan, Krati Shah, et al.American Journal of Medical Genetics. Part A|February 10, 2017
Blepharocheilodontic (BCD) syndrome: New insights on craniofacial and dental featuresWael Awadh, Anu Kiukkonen, Pekka Nieminen, et al.Pageof 928