P575: The Rare Genomes Project: Improving access to genomic sequencing and identifying causes of rare disease

التفاصيل البيبلوغرافية
العنوان:	P575: The Rare Genomes Project: Improving access to genomic sequencing and identifying causes of rare disease
المؤلفون:	Christina Austin-Tse, Stephanie DiTroia, Melanie O'Leary, Grace VanNoy, Brian Mangilog, Gulalai Shah, Eva Martinez, Jillian Serrano, Lynn Pais, Emily O'Heir, Ikeoluwa Osei-Owusu, Gabrielle Lemire, Vijay Ganesh, Sarah Stenton, Mutaz Amin, Kayla Socarras, Mugdha Singh, Stacey Hall, Katie Larsson, Moriel Singer-Berk, Daniel Marten, Michael Wilson, Hana Snow, Benjamin Blankenmeister, Jialan Ma, Ben Weisburd, Alba Sanchis-Juan, Harrison Brand, Emily Groopman, Alysia Lovgren, Clara Williamson, Marissa Hollyer, Eleina England, Eleanor Seaby, Katherine Chao, Julia Goodrich, Samantha Baxter, Daniel MacArthur, Michael Talkowski, Monica Wojcik, Anne O'Donnell-Luria, Heidi Rehm
المصدر:	Genetics in Medicine Open, Vol 2, Iss , Pp 101481- (2024)
بيانات النشر:	Elsevier, 2024.
سنة النشر:	2024
المجموعة:	LCC:Genetics LCC:Medicine
مصطلحات موضوعية:	Genetics, QH426-470, Medicine
نوع الوثيقة:	article
وصف الملف:	electronic resource
اللغة:	English
تدمد:	2949-7744
Relation:	http://www.sciencedirect.com/science/article/pii/S2949774424006277; https://doaj.org/toc/2949-7744
DOI:	10.1016/j.gimo.2024.101481
URL الوصول:	https://doaj.org/article/bdb5a2568ed74512805481c679dca743
رقم الأكسشن:	edsdoj.bdb5a2568ed74512805481c679dca743
قاعدة البيانات:	Directory of Open Access Journals

الوصف
تدمد:	29497744
DOI:	10.1016/j.gimo.2024.101481