Kết quả tìm kiếm - Mark J. Stephan
- Đang hiển thị 1 - 6 kết quả của 6
-
1
Aortic aneurysmal disease and cutis laxa caused by defects in the elastin gene Bằng Z. Szabó, Marc Crepeau, Alex Mitchell, Mark J. Stephan, Robert Puntel, Kah Yin Loke, Richard Kirk, Zsolt Urbán
Được phát hành 2005Carta -
2
Heterogeneous Pulmonary Phenotypes Associated With Mutations in the Thyroid Transcription Factor Gene NKX2-1 Bằng Aaron Hamvas, Robin R. Deterding, Susan E. Wert, Frances V. White, Megan K. Dishop, Danielle N. Alfano, Ann C. Halbower, Benjamin C Planer, Mark J. Stephan, Derek A. Uchida, Lee D. Williames, Jill A. Rosenfeld, Robert Roger Lebel, Lisa R. Young, F. Sessions Cole, Lawrence M. Nogee
Được phát hành 2013Artigo -
3
Mutations in LAMA1 Cause Cerebellar Dysplasia and Cysts with and without Retinal Dystrophy Bằng Kimberly A. Aldinger, Stephen J. Mosca, Martine Tétreault, Jennifer C. Dempsey, Gisele E. Ishak, Taila Hartley, Ian G. Phelps, Ryan E. Lamont, Diana R. O’Day, Donald Basel, Karen W. Gripp, Laura Baker, Mark J. Stephan, François Bernier, Kym M. Boycott, Jacek Majewski, Jillian S. Parboosingh, A. Micheil Innes, Dan Doherty
Được phát hành 2014Artigo -
4
Whole-Genome Analysis Reveals that Mutations in Inositol Polyphosphate Phosphatase-like 1 Cause Opsismodysplasia Bằng Jennifer E. Below, Dawn Earl, Kathryn M. Shively, Margaret J. McMillin, Joshua D. Smith, Emily H. Turner, Mark J. Stephan, L.I. Al-Gazali, Jozef Hertecant, David Chitayat, Sheila Unger, Daniel H. Cohn, Deborah Krakow, James M. Swanson, Elaine M. Faustman, Jay Shendure, Deborah A. Nickerson, Michael J. Bamshad
Được phát hành 2012Artigo -
5
Cohesin complex-associated holoprosencephaly Bằng Paul Kruszka, Seth Berger, Valentina Casà, Mike R. Dekker, Jenna Gaesser, Karin Weiss, Ariel F. Martinez, David R. Murdock, Raymond J. Louie, Eloise J. Prijoles, Angie Lichty, Oebele F. Brouwer, Evelien Zonneveld‐Huijssoon, Mark J. Stephan, Jacob S. Hogue, Ping Hu, Momoko Tanima-Nagai, Joshua L. Everson, Chitra Prasad, Anna Cereda, Maria Iascone, Allison Schreiber, Vickie Zurcher, Nicole Corsten‐Janssen, Luis Escobar, Nancy J. Clegg, Mauricio R. Delgado, Omkar Hajirnis, Meena Balasubramanian, Hülya Kayserili, Matthew A. Deardorff, Raymond A. Poot, Kerstin S. Wendt, Robert J. Lipinski, Maximilian Muenke
Được phát hành 2019Artigo -
6
Molecular analysis expands the spectrum of phenotypes associated with GLI3 mutations Bằng Jennifer J. Johnston, Julie C. Sapp, Joyce Turner, David J. Amor, Salim Aftimos, Kyrieckos A. Aleck, Maureen Bocian, Joann Bodurtha, Gerald F. Cox, Cynthia J. Curry, Ruth Day, Dian Donnai, Michael Field, Ikuma Fujiwara, Michael T. Gabbett, Moran Gal, John M. Graham, Peter Hedera, Raoul C. M. Hennekam, Joseph H. Hersh, Robert J. Hopkin, Hülya Kayserili, Alexa Kidd, Virginia Kimonis, Angela E. Lin, Sally Ann Lynch, Melissa K. Maisenbacher, Sahar Mansour, Julie McGaughran, Lakshmi Mehta, Helen Murphy, Margarita Raygada, Nathaniel H. Robin, Alan F. Rope, Kenneth N. Rosenbaum, G. Bradley Schaefer, Amy Shealy, Wendy E. Smith, Maria Soller, Annmarie Sommer, Heather J. Stalker, Bernhard Steiner, Mark J. Stephan, David Tilstra, Susan Tomkins, Pamela Trapane, Anne Chun-Hui Tsai, Margot I. Van Allen, Pradeep Vasudevan, Bernhard Zabel, Janice Zunich, Graeme Black, Leslie G. Biesecker
Được phát hành 2010Artigo
Công cụ tìm kiếm:
Các môn học liên quan
Biology
Genetics
Gene
Medicine
Phenotype
Pathology
Transcription factor
Aorta
Aortic aneurysm
Art
Art history
Biochemistry
Cancer research
Cohesin
Cutis laxa
Disease
Elastin
Endocrinology
Exome sequencing
Exon
Fetus
GLI3
Genotype
Genotype-phenotype distinction
Holoprosencephaly
Hum
Internal medicine
Meiosis
Mutation
Neuroscience