نتائج البحث - V. Reid Sutton
- يعرض 1 - 20 نتائج من 73
- اذهب إلى الاصفحة التالية
-
1
-
2
-
3
-
4
Neuroimaging aspects of Aicardi syndrome حسب Bobbi Hopkins, V. Reid Sutton, Richard A. Lewis, Ignatia Van den Veyver, Gary Clark
منشور في 2008Artigo -
5
<scp>P</scp> heno <scp>DB</scp> : A New Web‐Based Tool for the Collection, Storage, and Analysis of Phenotypic Features حسب Ada Hamosh, Nara Sobreira, Julie Hoover‐Fong, V. Reid Sutton, Corinne D. Boehm, François Schiettecatte, David Valle
منشور في 2013Artigo -
6
-
7
-
8
-
9
Chromosome 1p36 Deletions: The Clinical Phenotype and Molecular Characterization of a Common Newly Delineated Syndrome حسب Stuart K. Shapira, Christopher McCaskill, Hope Northrup, Aimee S. Spikes, F.F.B. Elder, V. Reid Sutton, Julie R. Korenberg, Frank Greenberg, Lisa G. Shaffer
منشور في 1997Artigo -
10
-
11
Comparison of Untargeted Metabolomic Profiling vs Traditional Metabolic Screening to Identify Inborn Errors of Metabolism حسب Ning Liu, Jing Xiao, Charul Gijavanekar, Kirk L. Pappan, Kevin E. Glinton, Brian J. Shayota, Adam D. Kennedy, Qin Sun, V. Reid Sutton, Sarah H. Elsea
منشور في 2021Artigo -
12
Elucidation of the complex metabolic profile of cerebrospinal fluid using an untargeted biochemical profiling assay حسب Adam D. Kennedy, Kirk L. Pappan, Taraka Donti, Anne M. Evans, Jacob Wulff, Luke A. D. Miller, V. Reid Sutton, Qin Sun, Marcus J. Miller, Sarah H. Elsea
منشور في 2017Artigo -
13
The long-term safety and efficacy of vestronidase alfa, rhGUS enzyme replacement therapy, in subjects with mucopolysaccharidosis VII حسب Raymond Wang, José Francisco da Silva Franco, Jaime López‐Valdez, Esmeralda Martins, V. Reid Sutton, Chester B. Whitley, Lin Zhang, Tricia Cimms, Deborah Marsden, Agnieszka Jurecka, Paul Harmatz
منشور في 2020Artigo -
14
Review of the phenotypic spectrum associated with haploinsufficiency of <i>MYRF</i> حسب Linda Rossetti, Kevin E. Glinton, Bo Yuan, Pengfei Liu, Nishitha R. Pillai, Elizabeth Mizerik, Pilar Magoulas, Jill A. Rosenfeld, Lefkothea Karaviti, V. Reid Sutton, Seema R. Lalani, Daryl A. Scott
منشور في 2019Revisão -
15
Untargeted metabolomic analysis for the clinical screening of inborn errors of metabolism حسب Marcus J. Miller, Adam D. Kennedy, Andrea D. Eckhart, Lindsay C. Burrage, Jacob Wulff, Luke A. D. Miller, Michael V. Milburn, John Ryals, Arthur L. Beaudet, Qin Sun, V. Reid Sutton, Sarah H. Elsea
منشور في 2015Artigo -
16
State of the art review in gonadal dysgenesis: challenges in diagnosis and management حسب Bonnie McCann‐Crosby, Roshanak Mansouri, Jennifer E. Dietrich, Laurence B. McCullough, V. Reid Sutton, Elise G. Austin, Bruce J. Schlomer, David R. Roth, Lefkothea Karaviti, Sheila Gunn, John Hicks, Charles G. Macias
منشور في 2014Artigo -
17
Clinical spectrum associated with recurrent genomic rearrangements in chromosome 17q12 حسب Sandesh C. Sreenath Nagamani, Ayelet Erez, Joseph Shen, Chumei Li, Elizabeth Roeder, Sarah K. Cox, Lefkothea Karaviti, Margret Pearson, Sung‐Hae Kang, Trilochan Sahoo, Seema R. Lalani, Paweł Stankiewicz, V. Reid Sutton, Sau Wai Cheung
منشور في 2009Artigo -
18
Diagnosis of adenylosuccinate lyase deficiency by metabolomic profiling in plasma reveals a phenotypic spectrum حسب Taraka Donti, Gerarda Cappuccio, Leroy Hubert, Juanita Neira, Paldeep S. Atwal, Marcus J. Miller, Aaron L. Cardon, V. Reid Sutton, Brenda E. Porter, Fiona M. Baumer, Michael F. Wangler, Qin Sun, Lisa Emrick, Sarah H. Elsea
منشور في 2016Artigo -
19
Liver transplantation in propionic and methylmalonic acidemia: A single center study with literature review حسب Nishitha R. Pillai, Bridget M. Stroup, Anna Poliner, Linda Rossetti, Brandy Rawls, Brian J. Shayota, Claudia Soler‐Alfonso, Hari Priya Tunuguntala, John A. Goss, William Craigen, Fernando Scaglia, V. Reid Sutton, Ryan Himes, Lindsay C. Burrage
منشور في 2019Revisão -
20
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes حسب Zhishuo Ou, Jonathan S. Berg, Hagith Yonath, Victoria B. Enciso, David T. Miller, Jonathan Picker, Tiffanee Lenzi, Catherine E. Keegan, V. Reid Sutton, John W. Belmont, A. Craig Chinault, James R. Lupski, Sau Wai Cheung, Elizabeth Roeder, Ankita Patel
منشور في 2008Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Medicine
Gene
Genetics
Internal medicine
Phenotype
Pathology
Exome sequencing
Bioinformatics
Pediatrics
Computational biology
Mutation
Allele
Computer science
Endocrinology
Exome
Biochemistry
Chemistry
Metabolomics
Intellectual disability
Missense mutation
Operating system
Osteogenesis imperfecta
Psychiatry
Chromosome
Disease
Environmental health
Gene duplication
Genome
Human genetics