অনুসন্ধান ফলাফলগুলি - Ethylin Wang Jabs
- প্রদর্শন 1 - 20 ফলাফল এর 67
- পরবর্তী পৃষ্ঠায় যান
-
1
Genetic basis of potential therapeutic strategies for craniosynostosis অনুযায়ী Heather Melville, Yingli Wang, Peter J. Taub, Ethylin Wang Jabs
প্রকাশিত 2010Revisão -
2
-
3
-
4
-
5
-
6
FGF/FGFR Signaling Coordinates Skull Development by Modulating Magnitude of Morphological Integration: Evidence from Apert Syndrome Mouse Models অনুযায়ী Neus Martínez‐Abadías, Yann Heuzé, Yingli Wang, Ethylin Wang Jabs, Kristina Aldridge, Joan T. Richtsmeier
প্রকাশিত 2011Artigo -
7
-
8
-
9
Development and preliminary evaluation of an online educational video about whole-genome sequencing for research participants, patients, and the general public অনুযায়ী Saskia C. Sanderson, Sabrina A. Suckiel, Micol Zweig, Erwin P. Böttinger, Ethylin Wang Jabs, Lynne D. Richardson
প্রকাশিত 2015Artigo -
10
-
11
-
12
-
13
-
14
-
15
-
16
-
17
-
18
The Ups and Downs of Mutation Frequencies during Aging Can Account for the Apert Syndrome Paternal Age Effect অনুযায়ী Song-Ro Yoon, Jian Qin, Rivka L. Glaser, Ethylin Wang Jabs, Nancy S. Wexler, Rebecca Z. Sokol, Norman Arnheim, Peter Calabrese
প্রকাশিত 2009Artigo -
19
<i>TCOF1</i> gene encodes a putative nucleolar phosphoprotein that exhibits mutations in Treacher Collins Syndrome throughout its coding region অনুযায়ী Carol A. Wise, Lydia C. Chiang, William A. Paznekas, Mridula Sharma, Maurice M. Musy, Jennifer Ashley, Michael Lovett, Ethylin Wang Jabs
প্রকাশিত 1997Artigo -
20
Advancing age has differential effects on DNA damage, chromatin integrity, gene mutations, and aneuploidies in sperm অনুযায়ী Andrew J. Wyrobek, Brenda Eskenazi, Suzanne Young, Norman Arnheim, Irene Tiemann‐Boege, Ethylin Wang Jabs, Rivka L. Glaser, Francesca Pearson, D.P. Evenson
প্রকাশিত 2006Artigo
অনুসন্ধান সাধনীগুলি:
সম্পর্কিত বিষয়
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