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American Journal of Medical Genetics. Part A|February 27, 2020
Expanding the spectrum of CEP55-associated disease to viable phenotypesElizabeth S Barrie, Eline Overwater, Mieke M van Haelst, et al.American Journal of Medical Genetics. Part A|February 27, 2020
Three-dimensional facial morphology in Cantú syndromeHelen I Roessler, Kathleen Shields, Dorothy K Grange, et al.American Journal of Medical Genetics. Part A|December 15, 2019
Cardiac manifestations and gene mutations of patients with RASopathies in TaiwanChung-Lin Lee, Louis Tan Hock-Cheong Tan, Hsiang-Yu Lin, et al.American Journal of Medical Genetics. Part A|December 17, 2019
Renpenning syndrome in a femaleRaymond Y Cho, Maria S Peñaherrera, Christele Du Souich, et al.American Journal of Medical Genetics. Part A|December 18, 2019
Palmoplantar keratoderma, oral involvement, and homozygous CTSC mutation in two brothers from CambodiaHeming Wei, Lynette W Y Wee, Bori Born, et al.American Journal of Medical Genetics. Part A|November 3, 2020
Genetic control of tumor development in malformation syndromesFloor A M Postema, Jan C Oosterwijk, Raoul C HennekamAmerican Journal of Medical Genetics. Part A|November 6, 2020
Genotype-phenotype correlation in seven motor neuron disease families with novel ALS2 mutationsRosanne Sprute, Hannah Jergas, Akgün Ölmez, et al.American Journal of Medical Genetics. Part A|February 10, 2019
Substantial pain burden in frequency, intensity, interference and chronicity among children and adults with neurofibromatosis Type 1Alanna M Kongkriangkai, Christopher King, Lisa J Martin, et al.American Journal of Medical Genetics. Part A|November 21, 2020
COFS type 3 in an Indian family with antenatally detected arthrogryposisInusha Panigrahi, Bangalore Anantharamu Shankar Prasad, Harleen Kaur, et al.American Journal of Medical Genetics. Part A|November 18, 2020
The spectrum of brain malformations and disruptions in twinsKaylee B Park, Teresa Chapman, Kimberly A Aldinger, et al.Pageof 928