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American Journal of Medical Genetics. Part A|January 17, 2012
Anthropometric charts for infants with trisomies 21, 18, or 13 born between 22 weeks gestation and term: the VON chartsNansi S Boghossian, Jeffrey D Horbar, Jeffrey C Murray, et al.American Journal of Medical Genetics. Part A|January 17, 2012
Mosaic tetrasomy 5p resulting from an isochromosome 5p marker chromosome: case report and review of literatureJo-Ann K Brock, Sarah Dyack, Mark Ludman, et al.American Journal of Medical Genetics. Part A|April 26, 2012
Informed consent for whole genome sequencing: a qualitative analysis of participant expectations and perceptions of risks, benefits, and harmsHolly K Tabor, Jacquie Stock, Tracy Brazg, et al.American Journal of Medical Genetics. Part A|April 19, 2012
Primary osteoporosis without features of OI in children and adolescents: clinical and genetic characteristicsChristine M Laine, Dror Koltin, Miki Susic, et al.American Journal of Medical Genetics. Part A|April 13, 2012
Enzyme replacement therapy improves joint motion and outcome of the 12-min walk test in a mucopolysaccharidosis type VI patient previously treated with bone marrow transplantationYoung Bae Sohn, Sung Won Park, Se-Hwa Kim, et al.American Journal of Medical Genetics. Part A|April 13, 2012
Somatic mosaicism and the phenotypic expression of COL2A1 mutationsSonali Nagendran, Allan J Richards, Annie McNinch, et al.American Journal of Medical Genetics. Part A|April 24, 2012
Sirenomelia and caudal malformations in two familiesMarion Gerard, Valérie Layet, Teresa Costa, et al.American Journal of Medical Genetics. Part A|April 25, 2012
Noonan syndrome due to a SHOC2 mutation presenting with fetal distress and fatal hypertrophic cardiomyopathy in a premature infantRebecca Hoban, Amy E Roberts, Laurie Demmer, et al.American Journal of Medical Genetics. Part A|April 25, 2012
Hypertension in FMR1 premutation males with and without fragile X-associated tremor/ataxia syndrome (FXTAS)Alyssa A Hamlin, Dina Sukharev, Luis Campos, et al.American Journal of Medical Genetics. Part A|September 13, 2011
Deletion 2p15-16.1 syndrome: case report and reviewPaolo Prontera, Laura Bernardini, Gabriela Stangoni, et al.Pageof 928