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1دورية أكاديمية
المؤلفون: Natalie Blagowidow, Beata Nowakowska, Erica Schindewolf, Francesca Romana Grati, Carolina Putotto, Jeroen Breckpot, Ann Swillen, Terrence Blaine Crowley, Joanne C. Y. Loo, Lauren A. Lairson, Sólveig Óskarsdóttir, Erik Boot, Sixto Garcia-Minaur, Maria Cristina Digilio, Bruno Marino, Beverly Coleman, Julie S. Moldenhauer, Anne S. Bassett, Donna M. McDonald-McGinn
المصدر: Genes, Vol 14, Iss 1, p 160 (2023)
مصطلحات موضوعية: prenatal ultrasound, 22q11.2 deletion syndrome, noninvasive prenatal screening, preimplantation genetic testing, fetal cardiac anomaly, Genetics, QH426-470
وصف الملف: electronic resource
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المؤلفون: Donna M. McDonald-McGinn, Emily Hoffman, Lauren A. Lairson, Daniel E. McGinn, Elaine H. Zackai
المصدر: The Chromosome 22q11.2 Deletion Syndrome ISBN: 9780128160473
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::56a0e5d21cb6cb1b2223bfe95fe3de11Test
https://doi.org/10.1016/b978-0-12-816047-3.00024-1Test -
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المؤلفون: Donna M. McDonald-McGinn, Emily Hoffman, Lauren A. Lairson, Daniel E. McGinn, Elaine H. Zackai
المصدر: The Chromosome 22q11.2 Deletion Syndrome ISBN: 9780128160473
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::1506c2c5af0a95e63931ad3054325c51Test
https://doi.org/10.1016/b978-0-12-816047-3.00018-6Test -
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المؤلفون: Anne S. Bassett, Jason P. Van Batavia, Erik Boot, Giulio Calcagni, René M. Castelein, Madeline Chadehumbe, Maria Corral, Maria Cristina Digilio, Lisa M. Elden, Ania Fiksinski, Brian John Forbes, Jessica Gold, Emily Hoffman, Jelle F. Homans, Stephen R. Hooper, Sarah Hopkins, Sarah Ivins, Oksana A. Jackson, Alison E. Kaye, Thomas F. Kolon, Rebecca E. Kotcher, Nehir Edibe Kurtas, Lauren A. Lairson, Michele P. Lambert, Lorraine E. Levitt Katz, Bruno Marino, Maria R. Mascarenhas, Donna M. McDonald-McGinn, Daniel E. McGinn, Julie S. Moldenhauer, Bernice E. Morrow, Edward M. Moss, Sólveig Óskarsdóttir, Carolina Putotto, Arpana Rayannavar, Peter Scambler, Erica M. Schindewolf, Cynthia B. Solot, Kathleen E. Sullivan, Ann Swillen, Marta Unolt, Lily Van, Joris Robert Vermeesch, Paolo Versacci, Jacob Vorstman, Elaine H. Zackai
المصدر: The Chromosome 22q11.2 Deletion Syndrome ISBN: 9780128160473
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::f28f5fb73bfabb3654b0ffdcad992719Test
https://doi.org/10.1016/b978-0-12-816047-3.09994-9Test -
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المصدر: The Chromosome 22q11.2 Deletion Syndrome ISBN: 9780128160473
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::9567b6b86115cd3c70c8dbf119a4ee0cTest
https://doi.org/10.1016/b978-0-12-816047-3.00025-3Test -
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المؤلفون: Stephen Tang, Vidyalakshmi Sethunath, Nebiyou Y. Metaferia, Marina F. Nogueira, Daniel S. Gallant, Emma R. Garner, Lauren A. Lairson, Christopher M. Penney, Jiao Li, Maya K. Gelbard, Sarah Abou Alaiwi, Ji-Heui Seo, Justin H. Hwang, Craig A. Strathdee, Sylvan C. Baca, Shatha AbuHammad, Xiaoyang Zhang, John G. Doench, William C. Hahn, David Y. Takeda, Matthew L. Freedman, Peter S. Choi, Srinivas R. Viswanathan
المصدر: Cell Rep
مصطلحات موضوعية: Male, Protein-Arginine N-Methyltransferases, Prostate, Prostatic Neoplasms, Androgen Antagonists, General Biochemistry, Genetics and Molecular Biology, Article, Gene Expression Regulation, Neoplastic, Repressor Proteins, Prostatic Neoplasms, Castration-Resistant, Receptors, Androgen, Cell Line, Tumor, Humans, Signal Transduction
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74705f949afe5f34a963ebc736db4285Test
https://pubmed.ncbi.nlm.nih.gov/35993121Test