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Revista Da Associacao Medica Brasileira (1992)|November 26, 2015
Menkes disease: importance of diagnosis with molecular analysis in the neonatal periodLarissa Sampaio de Athayde Costa, Stephanie Pucci Pegler, Rute Facchini Lellis, et al.
Nature Genetics|May 4, 2010
Genome-wide association study identifies variants at CSF1, OPTN and TNFRSF11A as genetic risk factors for Paget's disease of boneOmar M E Albagha, Micaela R Visconti, Nerea Alonso, et al.
Frontiers in Microbiology|February 16, 2026
Interspecies interactions among sugarcane-associated bacteria and their impact on plant growth promotion traitsCésar Justiniano Fascio, Anna Carolina Rubio Molina, Benyi Juliana Marin-Gallego, et al.
Plos One|May 5, 2017
Beneficial rhizobacteria immobilized in nanofibers for potential application as soybean seed bioinoculantsPriscilla Romina De Gregorio, Gabriela Michavila, Lenise Ricciardi Muller, et al.
American Journal of Medical Genetics. Part A|February 24, 2011
Cantú syndrome: report of nine new cases and expansion of the clinical phenotypeIngrid Scurr, Louise Wilson, Melissa Lees, et al.
American Journal of Medical Genetics. Part A|October 22, 2019
Nosology and classification of genetic skeletal disorders: 2019 revisionGeert R Mortier, Daniel H Cohn, Valerie Cormier-Daire, et al.
Retina (Philadelphia, Pa.)|March 9, 2023
OUTCOMES OF SWITCHING FROM PROACTIVE TO REACTIVE TREATMENT AFTER DEVELOPING ADVANCED CENTRAL NEOVASCULAR AGE-RELATED MACULAR DEGENERATIONElisa E Cornish, Vuong Nguyen, Martin Puzo, et al.
European Journal of Medical Genetics|October 5, 2010
Lung disease associated with periventricular nodular heterotopia and an FLNA mutationAlice Masurel-Paulet, Eric Haan, Elizabeth M Thompson, et al.
European Journal of Human Genetics : EJHG|November 23, 2020
Pathogenic variants causing ABL1 malformation syndrome cluster in a myristoyl-binding pocket and increase tyrosine kinase activityAlexander J M Blakes, Emily Gaul, Wayne Lam, et al.
American Journal of Medical Genetics. Part A|March 26, 2011
Nosology and classification of genetic skeletal disorders: 2010 revisionMatthew L Warman, Valerie Cormier-Daire, Christine Hall, et al.
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