Search Results - Ganapathi, Mythily

Genome sequencing for diagnosing rare diseases by Wojcik, Monica H. (Author) , Lemire, Gabrielle (Author) , Berger, Eva (Author) , Zaki, Maha S. (Author) , Wissmann, Mariel (Author) , Win, Wathone (Author) , White, Susan M. (Author) , Weisburd, Ben (Author) , Wieczorek, Dagmar (Author) , Waddell, Leigh B. (Author) , Verboon, Jeffrey M. (Author) , VanNoy, Grace E. (Author) , Töpf, Ana (Author) , Tan, Tiong Yang (Author) , Syrbe, Steffen (Author) , Strehlow, Vincent (Author) , Straub, Volker (Author) , Stenton, Sarah L. (Author) , Snow, Hana (Author) , Singer-Berk, Moriel (Author) , Silver, Josh (Author) , Shril, Shirlee (Author) , Seaby, Eleanor G. (Author) , Schneider, Ronen (Author) , Sankaran, Vijay G. (Author) , Sanchis-Juan, Alba (Author) , Russell, Kathryn A. (Author) , Reinson, Karit (Author) , Ravenscroft, Gianina (Author) , Radtke, Maximilian (Author) , Popp, Denny (Author) , Polster, Tilman (Author) , Platzer, Konrad (Author) , Pierce, Eric A. (Author) , Place, Emily M. (Author) , Pajusalu, Sander (Author) , Pais, Lynn (Author) , Õunap, Katrin (Author) , Osei-Owusu, Ikeoluwa (Author) , Opperman, Henry (Author) , Okur, Volkan (Author) , Oja, Kaisa Teele (Author) , O’Leary, Melanie (Author) , O’Heir, Emily (Author) , Morel, Chantal F. (Author) , Merkenschlager, Andreas (Author) , Marchant, Rhett G. (Author) , Mangilog, Brian E. (Author) , Madden, Jill A. (Author) , MacArthur, Daniel (Author) , Lovgren, Alysia (Author) , Lerner-Ellis, Jordan P. (Author) , Lin, Jasmine (Author) , Laing, Nigel (Author) , Hildebrandt, Friedhelm (Author) , Hentschel, Julia (Author) , Groopman, Emily (Author) , Goodrich, Julia (Author) , Gleeson, Joseph G. (Author) , Ghaoui, Roula (Author) , Genetti, Casie A. (Author) , Gburek-Augustat, Janina (Author) , Gazda, Hanna T. (Author) , Ganesh, Vijay S. (Author) , Ganapathi, Mythily (Author) , Gallacher, Lyndon (Author) , Fu, Jack M. (Author) , Evangelista, Emily (Author) , England, Eleina (Author) , Donkervoort, Sandra (Author) , DiTroia, Stephanie (Author) , Cooper, Sandra T. (Author) , Chung, Wendy K. (Author) , Christodoulou, John (Author) , Chao, Katherine R. (Author) , Cato, Liam D. (Author) , Bujakowska, Kinga M. (Author) , Bryen, Samantha J. (Author) , Brand, Harrison (Author) , Bönnemann, Carsten G. (Author) , Beggs, Alan H. (Author) , Baxter, Samantha M. (Author) , Bartolomaeus, Tobias (Author) , Agrawal, Pankaj B. (Author) , Talkowski, Michael (Author) , Austin-Tse, Christina (Author) , Jamra, Rami Abou (Author) , Rehm, Heidi L. (Author) , O’Donnell-Luria, Anne (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext

Clinical validity assessment of genes frequently tested on intellectual disability/autism sequencing panels by Riggs, Erin Rooney (Author) , Bingaman, Taylor I. (Author) , Barry, Carrie-Ann (Author) , Behlmann, Andrea (Author) , Bluske, Krista (Author) , Bostwick, Bret (Author) , Bright, Alison (Author) , Chen, Chun-An (Author) , Clause, Amanda R. (Author) , Dharmadhikari, Avinash V. (Author) , Ganapathi, Mythily (Author) , Gonzaga-Jauregui, Claudia (Author) , Grant, Andrew R. (Author) , Hughes, Madeline Y. (Author) , Kim, Se Rin (Author) , Krause, Amanda (Author) , Liao, Jun (Author) , Lumaka, Aimé (Author) , Mah, Michelle (Author) , Maloney, Caitlin M. (Author) , Mohan, Shruthi (Author) , Osei-Owusu, Ikeoluwa A. (Author) , Reble, Emma (Author) , Rennie, Olivia (Author) , Savatt, Juliann M. (Author) , Shimelis, Hermela (Author) , Siegert, Rebecca K. (Author) , Sneddon, Tam P. (Author) , Thaxton, Courtney (Author) , Toner, Kelly A. (Author) , Tran, Kien Trung (Author) , Webb, Ryan (Author) , Wilcox, Emma H. (Author) , Yin, Jiani (Author) , Zhuo, Xinming (Author) , Znidarsic, Masa (Author) , Martin, Christa Lese (Author) , Betancur, Catalina (Author) , Vorstman, Jacob A. S. (Author) , Miller, David T. (Author) , Schaaf, Christian P. (Author) ,

• Verlag, lizenzpflichtig, Volltext
• Verlag, lizenzpflichtig, Volltext