Хайлтын үр дүнгүүд - Matthew A. Deardorff
- 57-н 1 - 20 үр дүнгүүдийг харуулж байна
- Дараагийн хуудас руу очих
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Biochemical and Structural Characterization of HDAC8 Mutants Associated with Cornelia de Lange Syndrome Spectrum Disorders -н Christophe Decroos, Nicolas Christianson, Laura E. Gullett, Christine M. Bowman, Karen E. Christianson, Matthew A. Deardorff, D.W. Christianson
Хэвлэсэн 2015Artigo -
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Identification of a prenatal profile of Cornelia de Lange syndrome (CdLS): A review of 53 CdLS pregnancies -н Dinah Clark, Ilana Sherer, Matthew A. Deardorff, Janice L. B. Byrne, Kathleen M. Loomes, Małgorzata J.M. Nowaczyk, Laird G. Jackson, Ian D. Krantz
Хэвлэсэн 2012Revisão -
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Congenital heart disease in Cornelia de Lange syndrome: Phenotype and genotype analysis -н Kathryn C. Chatfield, Samantha A. Schrier, Jennifer Li, Dinah Clark, Maninder Kaur, Antonie D. Kline, Matthew A. Deardorff, Laird S. Jackson, Elizabeth Goldmuntz, Ian D. Krantz
Хэвлэсэн 2012Artigo -
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Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis -н Laura K. Conlin, Brian Thiel, Carsten G. Bönnemann, Līvija Medne, Linda M. Ernst, Elaine H. Zackai, Matthew A. Deardorff, Ian D. Krantz, Hákon Hákonarson, Nancy B. Spinner
Хэвлэсэн 2010Artigo -
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Mutations in the ABCC6 Gene as a Cause of Generalized Arterial Calcification of Infancy: Genotypic Overlap with Pseudoxanthoma Elasticum -н Qiaoli Li, Jill L. Brodsky, Laura K. Conlin, Bruce Pawel, Andrew C. Glatz, Rachel I. Gafni, Leon J. Schurgers, Jouni Uitto, Hákon Hákonarson, Matthew A. Deardorff, Michael A. Levine
Хэвлэсэн 2013Artigo -
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Causes of death and autopsy findings in a large study cohort of individuals with Cornelia de Lange syndrome and review of the literature -н Samantha A. Schrier, Ilana Sherer, Matthew A. Deardorff, Dinah Clark, Lynn Audette, Lynette A. Gillis, Antonie D. Kline, Linda M. Ernst, Kathleen M. Loomes, Ian D. Krantz, Laird G. Jackson
Хэвлэсэн 2011Revisão -
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16q24.3 Microdeletions Disrupting Upstream Non-Coding Region of ANKRD11 Cause KBG Syndrome -н Aiko Iwata‐Otsubo, Alyssa L. Rippert, Jorune Balciuniene, Sarah K. Fiordaliso, Robert Chen, Preetha Markose, Cara Skraban, Christopher Gray, Elaine H. Zackai, Holly Dubbs, Matthew A. Deardorff, Laura K. Conlin, Kosuke Izumi
Хэвлэсэн 2025Artigo -
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Transcriptional Dysregulation in NIPBL and Cohesin Mutant Human Cells -н Jinglan Liu, Zhe Zhang, Masashige Bando, Takehiko Itoh, Matthew A. Deardorff, Dinah Clark, Maninder Kaur, Stephany Tandy, Tatsuro Kondoh, Eric Rappaport, Nancy B. Spinner, Hugo Vega, Laird G. Jackson, Katsuhiko Shirahige, Ian D. Krantz
Хэвлэсэн 2009Artigo -
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Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith–Wiedemann syndrome -н Jennifer M. Kalish, Kara E. Boodhansingh, Tricia R. Bhatti, Arupa Ganguly, Laura K. Conlin, Susan Becker, Stephanie Givler, Lindsey Mighion, Andrew Palladino, N. Scott Adzick, Diva D. De León, Charles A. Stanley, Matthew A. Deardorff
Хэвлэсэн 2015Artigo -
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Characterization of the Beckwith‐Wiedemann spectrum: Diagnosis and management -н Kelly A. Duffy, Christopher M. Cielo︎, Jennifer L. Cohen, Christina X Gonzalez-Gandolfi, Jessica R. Griff, Evan R. Hathaway, Jonida Kupa, Jesse A. Taylor, Kathleen H. Wang, Arupa Ganguly, Matthew A. Deardorff, Jennifer M. Kalish
Хэвлэсэн 2019Artigo -
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The Coffin–Siris syndrome: A proposed diagnostic approach and assessment of 15 overlapping cases -н Samantha A. Schrier, Joann Bodurtha, Barbara K. Burton, Albert E. Chudley, Mary Anne D. Chiong, M D'Avanzo, Sally Ann Lynch, Antonio Musio, Dmitriy M. Nyazov, Pedro A. Sanchez‐Lara, Stavit A. Shalev, Matthew A. Deardorff
Хэвлэсэн 2012Artigo -
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Precision therapy for a new disorder of AMPA receptor recycling due to mutations in <i>ATAD1</i> -н Rebecca C. Ahrens‐Nicklas, George K. E. Umanah, Neal Sondheimer, Matthew A. Deardorff, Alisha Wilkens, Laura K. Conlin, Avni Santani, Addie I. Nesbitt, Jane Juulsola, Erica Ma, Ted M. Dawson, Valina L. Dawson, Eric D. Marsh
Хэвлэсэн 2017Artigo
Хайх хэрэгслүүд:
Холбогдох сэдвүүд
Biology
Genetics
Gene
Medicine
Mutation
Phenotype
Cornelia de Lange Syndrome
Internal medicine
Cell biology
Chromosome
Cohesin
Exome sequencing
Neuroscience
Pediatrics
Missense mutation
Pathology
Gene expression
Genome
Intellectual disability
Computer science
Disease
Phosphorylation
Psychology
Anatomy
Bioinformatics
Computational biology
DNA methylation
Karyotype
Loss function
Meiosis