Sökresultat - Strong, Emma

Symmetrical Dose-Dependent DNA-Methylation Profiles in Children with Deletion or Duplication of 7q11.23 av Strong, Emma, Butcher, Darci T., Singhania, Rajat, Mervis, Carolyn B., Morris, Colleen A., De Carvalho, Daniel, Weksberg, Rosanna, Osborne, Lucy R.

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Understanding the impact of 1q21.1 copy number variant av Harvard, Chansonette, Strong, Emma, Mercier, Eloi, Colnaghi, Rita, Alcantara, Diana, Chow, Eva, Martell, Sally, Tyson, Christine, Hrynchak, Monica, McGillivray, Barbara, Hamilton, Sara, Marles, Sandra, Mhanni, Aziz, Dawson, Angelika J, Pavlidis, Paul, Qiao, Ying, Holden, Jeanette J, Lewis, Suzanne ME, O'Driscoll, Mark, Rajcan-Separovic, Evica

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Copy Number Variant Discrepancy Resolution Using the ClinGen Dosage Sensitivity Map Results in Updated Clinical Interpretations in ClinVar av Riggs, Erin R., Nelson, Tristan, Merz, Andrew, Ackley, Todd, Bunke, Brian, Collins, Christin D., Collinson, Morag N., Fan, Yao-Shan, Goodenberger, McKinsey L., Golden, Denae M., Haglund-Hazy, Linda, Krgovic, Danijela, Lamb, Allen N., Lewis, Zoe, Li, Guang, Liu, Yajuan, Meck, Jeanne, Neufeld-Kaiser, Whitney, Runke, Cassandra K., Sanmann, Jennifer N., Stavropoulos, Dimitri J., Strong, Emma, Su, Meng, Tayeh, Marwan K., Vokac, Nadja Kokalj, Thorland, Erik C., Andersen, Erica, Martin, Christa L.

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