Результати пошуку - Pevsner, Jonathan
- Показ 1 - 20 результатів із 50
- На наступну сторінку
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The Contribution of Mosaic Variants to Autism Spectrum Disorder за авторством Freed, Donald, Pevsner, Jonathan
Опубліковано 2016Текст -
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The biology of the mammalian Krüppel-like family of transcription factors за авторством Dang, Duyen T., Pevsner, Jonathan, Yang, Vincent W.
Опубліковано 2000Текст -
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Somatic Mosaicism in the Human Genome за авторством Freed, Donald, Stevens, Eric L., Pevsner, Jonathan
Опубліковано 2014Текст -
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Sensitive and specific detection of mosaic chromosomal abnormalities using the Parent-of-Origin-based Detection (POD) method за авторством Baugher, Joseph D, Baugher, Benjamin D, Shirley, Matthew D, Pevsner, Jonathan
Опубліковано 2013Текст -
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Syntaxin 7 and VAMP-7 are Soluble N-Ethylmaleimide–sensitive Factor Attachment Protein Receptors Required for Late Endosome–Lysosome and Homotypic Lysosome Fusion in Alveolar Macro... за авторством Ward, Diane McVey, Pevsner, Jonathan, Scullion, Matthew A., Vaughn, Michael, Kaplan, Jerry
Опубліковано 2000Текст -
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Efficient Array-Based Identification of Novel Cardiac Genes through Differentiation of Mouse ESCs за авторством Miller, Ronald A., Christoforou, Nicolas, Pevsner, Jonathan, McCallion, Andrew S., Gearhart, John D.
Опубліковано 2008Текст -
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Mosaicism in Human Health and Disease за авторством Thorpe, Jeremy, Osei-Owusu, Ikeoluwa A., Avigdor, Bracha Erlanger, Tupler, Rossella, Pevsner, Jonathan
Опубліковано 2020Текст -
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Altered Patterns of Cellular Gene Expression in Dermal Microvascular Endothelial Cells Infected with Kaposi's Sarcoma-Associated Herpesvirus за авторством Poole, Lynn J., Yu, Yanxing, Kim, Peter S., Zheng, Qi-Zhi, Pevsner, Jonathan, Hayward, Gary S.
Опубліковано 2002Текст -
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Inference of Relationships in Population Data Using Identity-by-Descent and Identity-by-State за авторством Stevens, Eric L., Heckenberg, Greg, Roberson, Elisha D. O., Baugher, Joseph D., Downey, Thomas J., Pevsner, Jonathan
Опубліковано 2011Текст -
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A Novel Variantin GABRB2 Associated with Intellectual Disability and Epilepsy за авторством Srivastava, Siddharth, Cohen, Julie, Pevsner, Jonathan, Aradhya, Swaroop, McKnight, Dianalee, Butler, Elizabeth, Johnston, Michael, Fatemi, Ali
Опубліковано 2014Текст -
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Molecular (SNP) Analyses of Overlapping Hemizygous Deletions of 10q25.3 to 10qter in Four Patients: Evidence for HMX2 and HMX3 as Candidate Genes in Hearing and Vestibular Function за авторством Miller, Nathaniel D., Nance, Melonie A., Wohler, Elizabeth S., Hoover-Fong, Julie E., Lisi, Emily, Thomas, George H., Pevsner, Jonathan
Опубліковано 2009Текст -
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Identification of a mosaic activating mutation in GNA11 in atypical Sturge-Weber Syndrome за авторством Thorpe, Jeremy, Frelin, Laurence P., McCann, Meghan, Pardo, Carlos A., Cohen, Bernard A., Comi, Anne M., Pevsner, Jonathan
Опубліковано 2020Текст