Výsledky vyhledávání - Sally Rosengren
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Distinct Missense Mutations of the FGFR3 Lys650 Codon Modulate Receptor Kinase Activation and the Severity of the Skeletal Dysplasia Phenotype Autor Gary A. Bellus, Elaine Spector, Phyllis Speiser, Christine A. Weaver, A.T. Garber, Christine R. Bryke, Jamie Israel, Sally Rosengren, Melanie K. Webster, Daniel J. Donoghue, Clair A. Francomano
Vydáno 2000Artigo -
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Observation and prediction of recurrent human translocations mediated by NAHR between nonhomologous chromosomes Autor Zhishuo Ou, Paweł Stankiewicz, Zhilian Xia, Amy M. Breman, Brian Dawson, Joanna Wiszniewska, Przemysław Szafrański, M. Lance Cooper, Mitchell Rao, Lina Shao, Sarah T. South, Karlene Coleman, Paul M. Fernhoff, Marcel J. Deray, Sally Rosengren, Elizabeth Roeder, Victoria B. Enciso, A. Craig Chinault, Ankita Patel, Sung-Hae L. Kang, Chad A. Shaw, James R. Lupski, Sau Wai Cheung
Vydáno 2011Artigo -
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Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities Autor Nicola Brunetti‐Pierri, Jonathan S. Berg, Fernando Scaglia, John W. Belmont, Carlos A. Bacino, Trilochan Sahoo, Seema R. Lalani, Brett H. Graham, Brendan Lee, Marwan Shinawi, Joseph Shen, Sung-Hae L. Kang, Amber N. Pursley, Timothy Lotze, Gail Kennedy, Susan Lansky-Shafer, Christine A. Weaver, Elizabeth Roeder, Theresa A. Grebe, Georgianne L. Arnold, Terry Hutchison, Tyler Reimschisel, Stephen Amato, Michael T Geragthy, Jeffrey W. Innis, Ewa Obersztyn, Beata Nowakowska, Sally Rosengren, Patricia I. Bader, Dorothy K. Grange, Sayed Naqvi, Adolfo D. Garnica, Saunder Bernes, Chin-To Fong, Anne Summers, William D. Walters, James R. Lupski, Paweł Stankiewicz, Sau Wai Cheung, Ankita Patel
Vydáno 2008Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Medicine
Mutation
Phenotype
Achondroplasia
Anatomy
Aqueduct
Archaeology
Audiology
Autism
Cancer research
Chromosomal translocation
Chromosome
Comparative genomic hybridization
Computational biology
Copy-number variation
Developmental disorder
Dysplasia
Exon
Fibroblast growth factor
Fibroblast growth factor receptor 3
Genetic recombination
Genome
Geography
Homologous recombination
Kinase
Locus (genetics)
Macrocephaly