Kết quả tìm kiếm - Ethylin Wang Jabs
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Genetic basis of potential therapeutic strategies for craniosynostosis Bằng Heather Melville, Yingli Wang, Peter J. Taub, Ethylin Wang Jabs
Được phát hành 2010Revisão -
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The human aquaporin-CHIP gene. Structure, organization, and chromosomal localization Bằng Chulso Moon, Gregory M. Preston, C.A. Griffin, Ethylin Wang Jabs, Peter Agre
Được phát hành 1993Artigo -
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FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models Bằng Neus Martínez‐Abadías, Yann Heuzé, Yingli Wang, Ethylin Wang Jabs, Kristina Aldridge, Joan T. Richtsmeier
Được phát hành 2011Artigo -
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Ten-year experience of more than 35,000 orofacial clefts in Africa Bằng Julia C Conway, Peter J. Taub, Rochelle Kling, Kurun Oberoi, John Doucette, Ethylin Wang Jabs
Được phát hành 2015Artigo -
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Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public Bằng Saskia C. Sanderson, Sabrina A. Suckiel, Micol Zweig, Erwin P. Böttinger, Ethylin Wang Jabs, Lynne D. Richardson
Được phát hành 2015Artigo -
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Mapping the Treacher Collins syndrome locus to 5q31.3→q33.3 Bằng Ethylin Wang Jabs, Xiang Li, Cathleen A. Coss, Eugene W. Taylor, Deborah A. Meyers, James L. Weber
Được phát hành 1991Artigo -
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Clinical spectrum of fibroblast growth factor receptor mutations Bằng M.R. Passos-Bueno, W.R. Wilcox, Ethylin Wang Jabs, Andréa L. Sertié, Luís Garcia Alonso, H. Kitoh
Được phát hành 1999Artigo -
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<i>TCOF1</i> gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region Bằng Carol A. Wise, Lydia C. Chiang, William A. Paznekas, Mridula Sharma, Maurice M. Musy, Jennifer Ashley, Michael Lovett, Ethylin Wang Jabs
Được phát hành 1997Artigo -
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Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm Bằng Andrew J. Wyrobek, Brenda Eskenazi, Suzanne Young, Norman Arnheim, Irene Tiemann‐Boege, Ethylin Wang Jabs, Rivka L. Glaser, Francesca Pearson, D.P. Evenson
Được phát hành 2006Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Genetics
Gene
Medicine
Mutation
Phenotype
Craniosynostosis
Craniofacial
Internal medicine
Receptor
Cell biology
Genotype
Missense mutation
Fibroblast growth factor
Molecular biology
Anatomy
Apert syndrome
Fibroblast growth factor receptor
Biochemistry
Chromosome
Genome
Pathology
Allele
Computer science
Connexin
Endocrinology
Fibroblast growth factor receptor 1
Gap junction
Intracellular
Mutant