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Clinical Genetics|June 1, 1989
A pseudoisochromosome 18q and an isodicentric chromosome 18C Floore, A Robertson, I Samuel, et al.
Clinical Genetics|September 12, 2017
mTOR mutations in Smith-Kingsmore syndrome: Four additional patients and a reviewG Gordo, J Tenorio, P Arias, et al.
Clinical Genetics|February 20, 2018
Expanding the histopathological spectrum of CFL2-related myopathiesF Fattori, C Fiorillo, C Rodolico, et al.
Clinical Genetics|March 2, 2018
ZNF687 mutations are frequently found in pagetic patients from South Italy: implication in the pathogenesis of Paget's disease of boneG Divisato, F Scotto di Carlo, N Petrillo, et al.
Clinical Genetics|February 1, 2018
Disclosure of cardiac variants of uncertain significance results in an exome cohortT A Lawal, K L Lewis, J J Johnston, et al.
Clinical Genetics|February 3, 2018
De novo variants in CDK13 associated with syndromic ID/DD: Molecular and clinical delineation of 15 individuals and a further reviewW M R van den Akker, I Brummelman, L M Martis, et al.
Clinical Genetics|January 25, 2018
Autosomal-dominant myopia associated to a novel P4HA2 missense variant and defective collagen hydroxylationF Napolitano, V Di Iorio, F Testa, et al.
Clinical Genetics|November 1, 1985
Two different clinical and genetic forms of hereditary palmoplantar keratoderma in the northernmost county of SwedenP Gamborg Nielsen
Clinical Genetics|January 18, 2019
Difficulties and challenges in the development of precision medicineXiaoqin Liu, Xin Luo, Chunyang Jiang, et al.
Clinical Genetics|January 18, 2019
Newly identified set of obesity-related genotypes and abdominal fat influence the risk of insulin resistance in a Korean populationMinjoo Kim, Sarang Jeong, Hye Jin Yoo, et al.
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