Søgeresultater - Tryon, Rebecca
- Showing 1 - 5 results of 5
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1
Comparable Outcomes after HLA-Matched Sibling and Alternative Donor Hematopoietic Cell Transplantation for Children with Fanconi Anemia and Severe Aplastic Anemia af Ebens, Christen L., DeFor, Todd E., Tryon, Rebecca, Wagner, John E., MacMillan, Margaret L.
Udgivet 2017Text -
2
Structural equation modeling of food craving across the menstrual cycle using behavioral, neuroendocrine, and metabolic factors af Krishnan, Sridevi, Agrawal, Karan, Tryon, Rebecca R., Welch, Lucas C., Horn, William F., Newman, John W., Keim, Nancy L.
Udgivet 2018Text -
3
A homozygous frameshift variant in the KRT5 gene is compatible with life and results in severe recessive epidermolysis bullosa simplex af Tryon, Rebecca K., Tolar, Jakub, Preusser, Sarah M., Riddle, Megan J., Keene, Douglas R., Bower, Matthew, Thyagarajan, Bharat, Ebens, Christen L.
Udgivet 2019Text -
4
Paternal or maternal uniparental disomy of chromosome 16 resulting in homozygosity of a mutant allele causes Fanconi anemia af Donovan, Frank X., Kimble, Danielle C., Kim, Yonghwan, Lach, Francis P., Harper, Ursula, Kamat, Aparna, Jones, MaryPat, Sanborn, Erica M., Tryon, Rebecca, Wagner, John E., MacMillan, Margaret L., Ostrander, Elaine A., Auerbach, Arleen D., Smogorzewska, Agata, Chandrasekharappa, Settara C.
Udgivet 2016Text -
5
De novo truncating variants in the AHDC1 gene encoding the AT-hook DNA-binding motif-containing protein 1 are associated with intellectual disability and developmental delay af Yang, Hui, Douglas, Ganka, Monaghan, Kristin G., Retterer, Kyle, Cho, Megan T., Escobar, Luis F., Tucker, Megan E., Stoler, Joan, Rodan, Lance H., Stein, Diane, Marks, Warren, Enns, Gregory M., Platt, Julia, Cox, Rachel, Wheeler, Patricia G., Crain, Carrie, Calhoun, Amy, Tryon, Rebecca, Richard, Gabriele, Vitazka, Patrik, Chung, Wendy K.
Udgivet 2015Text