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Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...Genetics in Medicine Open, 2024, Vol.2, p.101481, Article 101481
- Austin-Tse, Christina
- DiTroia, Stephanie
- O'Leary, Melanie
- VanNoy, Grace
- Mangilog, Brian
- Shah, Gulalai
- Martinez, Eva
- Serrano, Jillian
- Pais, Lynn
- O'Heir, Emily
- Osei-Owusu, Ikeoluwa
- Lemire, Gabrielle
- Ganesh, Vijay
- Stenton, Sarah
- Amin, Mutaz
- Socarras, Kayla
- Singh, Mugdha
- Hall, Stacey
- Larsson, Katie
- Singer-Berk, Moriel
- Marten, Daniel
- Wilson, Michael
- Snow, Hana
- Blankenmeister, Benjamin
- Ma, Jialan
- Weisburd, Ben
- Sanchis-Juan, Alba
- Brand, Harrison
- Groopman, Emily
- Lovgren, Alysia
- Williamson, Clara
- Hollyer, Marissa
- England, Eleina
- Seaby, Eleanor
- Chao, Katherine
- Goodrich, Julia
- Baxter, Samantha
- MacArthur, Daniel
- Talkowski, Michael
- Wojcik, Monica
- O'Donnell-Luria, Anne
- Rehm, Heidi
2024
Volltextzugriff (PDF)
American journal of human genetics, 2023-08, Vol.110 (8), p.1229-1248
- Wojcik, Monica H.
- Reuter, Chloe M.
- Marwaha, Shruti
- Mahmoud, Medhat
- Duyzend, Michael H.
- Barseghyan, Hayk
- Yuan, Bo
- Boone, Philip M.
- Groopman, Emily E.
- Délot, Emmanuèle C.
- Jain, Deepti
- Sanchis-Juan, Alba
- Starita, Lea M.
- Talkowski, Michael
- Montgomery, Stephen B.
- Bamshad, Michael J.
- Chong, Jessica X.
- Wheeler, Matthew T.
- Berger, Seth I.
- O'Donnell-Luria, Anne
- Sedlazeck, Fritz J.
- Miller, Danny E.
2023
Volltextzugriff (PDF)
Genetics in medicine, 2024-10, Vol.26 (10), p.101199, Article 101199
- Chong, Jessica X.
- Berger, Seth I.
- Baxter, Samantha
- Hawley, Megan H.
- DiTroia, Stephanie
- Alvarez, Raquel
- Amin, Mutaz
- Assimes, Themistocles
- Auriga, Light
- Bamshad, Mike
- Behera, Sairam
- Blankenmeister, Benjamin
- Blue, Elizabeth
- Bonner, Devon
- Boone, Philip
- Brand, Harrison
- Chavez, Clarisa
- Chen, Ziwei
- Cui, Ya Allen
- Currin, Sara
- Daber, Robert
- Dardas, Zain
- Davis, Colleen
- Dawood, Moez
- Doddapaneni, Harsha
- Duong, Nhat
- Duyzend, Michael
- Eichler, Evan
- Emami, Sara
- Fraser, Jamie
- Fusaro, Vincent
- Garcia, Brandon
- Garimella, Kiran
- Gifford, Casey
- Goddard, Page
- Gogarten, Stephanie
- Gogate, Nikhita
- Sousa, Rodrigo Guarischi
- Gudmundsson, Sanna
- Gulati, Ashima
- Hall, Stacey
- Harvey, William
- Horike-Pyne, Martha
- Hu, Jianhong
- Saad, Ahmed K.
- Knoblach, Susan
- Ko, Arthur
- Kundaje, Anshul
- Kundu, Soumya
- Larsson, Katie
- Lemire, Gabrielle
- Li, Yidan
- LoTempio, Jonathan
- Ma, Jialan
- Mahmoud, Medhat
- Malani, Nirav
- Mangilog, Brian
- Martinez, Eva
- Mastrorosa, Francesco Kumara
- Matalon, Dena
- May, Susanne
- Meador, Lauren
- Mitani, Tadahiro
- Montgomery, Stephen
- Moyses, Mariana
- Munderloh, Chloe
- Muzny, Donna
- Nykamp, Keith
- O'Callaghan, William
- Pan, Miao
- Panchal, Piyush
- Payne, Sheryl
- Petrowski, Paul
- Porter, Elizabeth
- Prosser, Jaime
- Quertermous, Thomas
- Rai, Archana
- Rivera-Munoz, Andres
- Sabo, Aniko
- Samocha, Kaitlin
- Savage, Sarah
- Shah, Gulalai
- Singh, Mugdha
- Smith, Kevin
- Smith, Josh
- Starita, Lea
- Stenton, Sarah
- Stilp, Adrienne
- Sutton, V. Reid
- Tong, Catherine (Cat)
- Tsao, Philip
- Ungar, Rachel
- Vilain, Eric
- Wei, Chia-Lin
- Weisburd, Ben
- Wellington, Chris
- Westheimer, Emily
- Wheeler, Marsha
- Wojcik, Monica
- Yadav, Rachita
2024
Volltextzugriff (PDF)
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- Candidate Gene
- Diagnostics
- Exome - Genetics
- Exome Reanalysis
- Exome Sequencing
- Gene Discovery
- Genetic Testing
- Genetics & Heredity
- Humans
- Life Sciences & Biomedicine
- Long-Read Sequencing
- Meatabolomics
- Mendelian Disorder
- Nanopore Sequencing
- Non-Diagnostic Exome
- Optical Genome Mapping
- Pacbio Sequencing
- Phenotype
- Rare Disease
- Rare Diseases
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