Výsledky vyhledávání - Debra Freedenberg
- Zobrazuji výsledky 1 - 10 z 10
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The incidence of urea cycle disorders Autor Marshall Summar, Stefan Koelker, Debra Freedenberg, Cynthia Le Mons, Johannes Häberle, Hye‐Seung Lee, Brian Kirmse
Vydáno 2013Artigo -
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Comprehensive Evaluation of the Child With Intellectual Disability or Global Developmental Delays Autor John B. Moeschler, Michael Shevell, John B. Moeschler, Michael Shevell, Robert A. Saul, Emily Chen, Debra Freedenberg, Rizwan Hamid, Marilyn C. Jones, Joan M. Stoler, Beth A. Tarini
Vydáno 2014Revisão -
4
A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency Autor Georgianne L. Arnold, Johan Van Hove, Debra Freedenberg, Arnold W. Strauss, Nicola Longo, Barbara K. Burton, Cheryl Garganta, Can Fıçıcıoğlu, Stephen Cederbaum, Cary O. Harding, Richard G. Boles, Dietrich Matern, Pranesh Chakraborty, Annette Feigenbaum
Vydáno 2009Artigo -
5
Relapsing diabetes can result from moderately activating mutations in KCNJ11 Autor Anna L. Gloyn, Frank Reimann, Christophe A. Girard, Emma L. Edghill, Peter Proks, Ewan R. Pearson, I. Karen Temple, Deborah Mackay, Julian Hamilton‐Shield, Debra Freedenberg, Kathryn Noyes, Sian Ellard, Frances M. Ashcroft, Fiona M. Gribble, Andrew T. Hattersley
Vydáno 2005Artigo -
6
Health Supervision for Children With Neurofibromatosis Type 1 Autor David T. Miller, Debra Freedenberg, Elizabeth K. Schorry, Nicole J. Ullrich, David Viskochil, Bruce R. Korf, Emily Chen, Tracy L. Trotter, Susan A. Berry, Leah W. Burke, Timothy A. Geleske, Rizwan Hamid, Robert J. Hopkin, Wendy J. Introne, Michael J. Lyons, Angela E. Scheuerle, Joan M. Stoler
Vydáno 2019Revisão -
7
Speech delay and autism spectrum behaviors are frequently associated with duplication of the 7q11.23 Williams-Beuren syndrome region Autor Jonathan S. Berg, Nicola Brunetti‐Pierri, Sarika U. Peters, Sung-Hae L. Kang, Chin-To Fong, Jessica Salamone, Debra Freedenberg, Vickie Hannig, Lisa Albers Prock, David T. Miller, Peter Raffalli, D. James Harris, Robert P. Erickson, Christopher Cunniff, Gary Clark, Maria Blazo, Daniel A. Peiffer, Kevin L. Gunderson, Trilochan Sahoo, Ankita Patel, James R. Lupski, Arthur L. Beaudet, Sau Wai Cheung
Vydáno 2007Artigo -
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Increased MECP2 gene copy number as the result of genomic duplication in neurodevelopmentally delayed males Autor Daniela del Gaudio, Ping Fang, Fernando Scaglia, Patricia A. Ward, William J. Craigen, Daniel G. Glaze, Jeffrey L. Neul, Ankita Patel, Jennifer A. Lee, Mira Irons, Susan A. Berry, Amber A. Pursley, Theresa A. Grebe, Debra Freedenberg, Rick A. Martin, Gary Hsich, Jena R Khera, Neil Friedman, Huda Y. Zoghbi, Christine M. Eng, James R. Lupski, Arthur L. Beaudet, Sau Wai Cheung, Benjamin B. Roa
Vydáno 2006Artigo -
9
Chromosome Catastrophes Involve Replication Mechanisms Generating Complex Genomic Rearrangements Autor Pengfei Liu, Ayelet Erez, Sandesh C. Sreenath Nagamani, Shweta U. Dhar, Katarzyna Kołodziejska, Avinash V. Dharmadhikari, M. Lance Cooper, Joanna Wiszniewska, Feng Zhang, Marjorie Withers, Carlos A. Bacino, Luis Daniel Campos-Acevedo, Mauricio R. Delgado, Debra Freedenberg, Adolfo D. Garnica, Theresa A. Grebe, Dolores Hernández-Almaguer, LaDonna Immken, Seema R. Lalani, Scott D. McLean, Hope Northrup, Fernando Scaglia, Lane Strathearn, Pamela Trapane, Sung-Hae L. Kang, Ankita Patel, Sau Wai Cheung, P. J. Hastings, Paweł Stankiewicz, James R. Lupski, Weimin Bi
Vydáno 2011Artigo -
10
Newborn Screening for Severe Combined Immunodeficiency in 11 Screening Programs in the United States Autor Antonia Kwan, Roshini S. Abraham, Robert J. Currier, Amy Brower, Karen Andruszewski, Jordan K. Abbott, Mei Baker, Mark Ballow, Louis Bartoshesky, Francisco A. Bonilla, Charles D. Brokopp, Edward G. Brooks, Michele Caggana, Jocelyn Celestin, Joseph A. Church, Anne Marie Comeau, James A. Connelly, Morton J. Cowan, Charlotte Cunningham‐Rundles, Trivikram Dasu, Nina Dave, M. Teresa de la Morena, Ulrich Duffner, Chin-To Fong, Lisa R. Forbes, Debra Freedenberg, Erwin W. Gelfand, Jaime E. Hale, I. Celine Hanson, Beverly N. Hay, Diana Hu, Anthony J. Infante, Daisy Johnson, Neena Kapoor, Denise M. Kay, Donald B. Kohn, Rachel Lee, Heather K. Lehman, Zhili Lin, Fred Lorey, Aly Abdel‐Mageed, Adrienne Manning, Sean McGhee, Theodore B. Moore, Stanley J. Naides, Luigi D. Notarangelo, Jordan S. Orange, Sung‐Yun Pai, Matthew H. Porteus, Ray Rodríguez, Neil Romberg, John M. Routes, Mary Ruehle, Arye Rubenstein, Carlos A. Saavedra‐Matiz, G. E. M. Scott, Patricia M. Scott, Elizabeth Secord, Christine M. Seroogy, William T. Shearer, Subhadra Siegel, Stacy K. Silvers, E. Richard Stiehm, Robert W. Sugerman, John L. Sullivan, Susan Tanksley, Millard L. Tierce, James Verbsky, Beth Vogel, Roz Walker, Kelly Walkovich, Jolán E. Walter, Richard L. Wasserman, Michael S. Watson, Geoffrey A. Weinberg, Leonard B. Weiner, Heather Wood, Anne Yates, Jennifer M. Puck
Vydáno 2014Artigo
Vyhledávací nástroje:
Související témata
Medicine
Gene
Biology
Genetics
Phenotype
Chemistry
Genome
Mutation
Pathology
Pediatrics
Psychiatry
Biochemistry
Comparative genomic hybridization
Copy-number variation
Environmental health
Gene duplication
Incidence (geometry)
Intellectual disability
Intensive care medicine
Internal medicine
Population
Proband
Alternative medicine
Amino acid
Arginine
Autism
Autism spectrum disorder
Breakpoint
Chromosomal translocation
Chromosome