التفاصيل البيبلوغرافية
العنوان: |
Genome-based newborn screening for severe childhood genetic diseases has high positive predictive value and sensitivity in a NICU pilot trial |
المؤلفون: |
Kingsmore, Stephen F., Wright, Meredith, Olsen, Lauren, Schultz, Brandan, Protopsaltis, Liana, Averbuj, Dan, Blincow, Eric, Carroll, Jeanne, Caylor, Sara, Defay, Thomas, Ellsworth, Katarzyna, Feigenbaum, Annette, Gover, Mia, Guidugli, Lucia, Hansen, Christian, Van Der Kraan, Lucita, Kunard, Chris M., Kwon, Hugh, Madhavrao, Lakshminarasimha, Leipzig, Jeremy, Liang, Yupu, Mardach, Rebecca, Mowrey, William R., Nguyen, Hung, Niemi, Anna-Kaisa, Oh, Danny, Saad, Muhammed, Scharer, Gunter, Schleit, Jennifer, Mehtalia, Shyamal S., Sanford, Erica, Smith, Laurie D., Willis, Mary J., Wigby, Kristen, Reimers, Rebecca |
المصدر: |
The American Journal of Human Genetics ; volume 111, issue 12, page 2643-2667 ; ISSN 0002-9297 |
بيانات النشر: |
Elsevier BV |
سنة النشر: |
2024 |
المجموعة: |
ScienceDirect (Elsevier - Open Access Articles via Crossref) |
نوع الوثيقة: |
article in journal/newspaper |
اللغة: |
English |
DOI: |
10.1016/j.ajhg.2024.10.020 |
الاتاحة: |
https://doi.org/10.1016/j.ajhg.2024.10.020 https://api.elsevier.com/content/article/PII:S0002929724003902?httpAccept=text/xml https://api.elsevier.com/content/article/PII:S0002929724003902?httpAccept=text/plain |
Rights: |
https://www.elsevier.com/tdm/userlicense/1.0/ ; https://www.elsevier.com/legal/tdmrep-license ; http://www.elsevier.com/open-access/userlicense/1.0/ |
رقم الانضمام: |
edsbas.D7041657 |
قاعدة البيانات: |
BASE |