অনুসন্ধান ফলাফলগুলি - Conta, Jessie H
- প্রদর্শন 1 - 4 ফলাফল এর 4
-
1
Single Nucleotide Polymorphism (SNP) Arrays and Unexpected Consanguinity: Considerations for Clinicians When Returning Results to Families অনুযায়ী Delgado, Fernanda, Tabor, Holly K., Chow, Penny M., Conta, Jessie H., Feldman, Kenneth W., Tsuchiya, Karen D., Beck, Anita E.
প্রকাশিত 2014পাঠ্য -
2
Practices and Policies of Clinical Exome Sequencing Providers: Analysis and Implications অনুযায়ী Jamal, Seema M., Yu, Joon-Ho, Chong, Jessica X., Dent, Karin M., Conta, Jessie H., Tabor, Holly K., Bamshad, Michael J.
প্রকাশিত 2013পাঠ্য -
3
A Novel Missense Mutation in POMT1 Modulates the Severe Congenital Muscular Dystrophy Phenotype Associated with POMT1 Nonsense Mutations অনুযায়ী Wallace, Stephanie E., Conta, Jessie H., Winder, Thomas L., Willer, Tobias, Eskuri, Jamie M., Haas, Richard, Patterson, Kathleen, Campbell, Kevin P., Moore, Steven A., Gospe, Sidney M.
প্রকাশিত 2014পাঠ্য -
4
The Koolen-de Vries syndrome: a phenotypic comparison of patients with a 17q21.31 microdeletion versus a KANSL1 sequence variant অনুযায়ী Koolen, David A, Pfundt, Rolph, Linda, Katrin, Beunders, Gea, Veenstra-Knol, Hermine E, Conta, Jessie H, Fortuna, Ana Maria, Gillessen-Kaesbach, Gabriele, Dugan, Sarah, Halbach, Sara, Abdul-Rahman, Omar A, Winesett, Heather M, Chung, Wendy K, Dalton, Marguerite, Dimova, Petia S, Mattina, Teresa, Prescott, Katrina, Zhang, Hui Z, Saal, Howard M, Hehir-Kwa, Jayne Y, Willemsen, Marjolein H, Ockeloen, Charlotte W, Jongmans, Marjolijn C, Van der Aa, Nathalie, Failla, Pinella, Barone, Concetta, Avola, Emanuela, Brooks, Alice S, Kant, Sarina G, Gerkes, Erica H, Firth, Helen V, Õunap, Katrin, Bird, Lynne M, Masser-Frye, Diane, Friedman, Jennifer R, Sokunbi, Modupe A, Dixit, Abhijit, Splitt, Miranda, Kukolich, Mary K, McGaughran, Julie, Coe, Bradley P, Flórez, Jesús, Nadif Kasri, Nael, Brunner, Han G, Thompson, Elizabeth M, Gecz, Jozef, Romano, Corrado, Eichler, Evan E, de Vries, Bert BA
প্রকাশিত 2016পাঠ্য