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Molecular Genetics & Genomic Medicine|January 8, 2016
Identification of an Alu-repeat-mediated deletion of OPTN upstream region in a patient with a complex ocular phenotypeKala F Schilter, Linda M Reis, Elena A Sorokina, et al.
Molecular Genetics & Genomic Medicine|January 8, 2016
Testicular dysgenesis/regression without campomelic dysplasia in patients carrying missense mutations and upstream deletion of SOX9Yuko Katoh-Fukui, Maki Igarashi, Keisuke Nagasaki, et al.
Molecular Genetics & Genomic Medicine|January 21, 2016
The dentin phosphoprotein repeat region and inherited defects of dentinJie Yang, Kazuhiko Kawasaki, Moses Lee, et al.
Molecular Genetics & Genomic Medicine|January 21, 2016
Allelic variants of the Melanocortin 4 receptor (MC4R) gene in a South African study groupMurray Logan, Maria-Teresa Van der Merwe, Tyren M Dodgen, et al.
Molecular Genetics & Genomic Medicine|January 21, 2016
Mid1/Mid2 expression in craniofacial development and a literature review of X-linked opitz syndromeBijun Li, Tianhong Zhou, Yi Zou
Molecular Genetics & Genomic Medicine|June 2, 2016
Medical genetics and genomic medicine in the Dominican Republic: challenges and opportunitiesJuvianee I Estrada-Veras, Giselle A Cabrera-Peña, Ceila Pérez-Estrella de Ferrán
Molecular Genetics & Genomic Medicine|June 2, 2016
Sideroblastic anemia: functional study of two novel missense mutations in ALAS2Manuel Méndez, María-Isabel Moreno-Carralero, Marta Morado-Arias, et al.
Molecular Genetics & Genomic Medicine|June 2, 2016
Development of a diagnostic DNA chip to screen for 30 autosomal recessive disorders in the Hutterite populationBarbara Triggs-Raine, Tamara Dyck, Kym M Boycott, et al.
Molecular Genetics & Genomic Medicine|June 2, 2016
ErratumJosephine Wincent, Aron Luthman, Martine van Belzen, et al.
Molecular Genetics & Genomic Medicine|April 12, 2016
Chromosome loci vary by juvenile myoclonic epilepsy subsyndromes: linkage and haplotype analysis applied to epilepsy and EEG 3.5-6.0 Hz polyspike wavesJenny E Wight, Viet-Huong Nguyen, Marco T Medina, et al.
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