Результати пошуку - Michella Ghassibe‐Sabbagh
- Показ 1 - 8 результатів із 8
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1
Interferon regulatory factor-6: a gene predisposing to isolated cleft lip with or without cleft palate in the Belgian population за авторством Michella Ghassibe‐Sabbagh, Bénédicte Bayet, Nicole Revençu, Christine Verellen‐Dumoulin, Y. Gillerot, R Vanwijck, Miikka Vikkula
Опубліковано 2005Artigo -
2
Mutations in a Novel Factor, Glomulin, Are Responsible for Glomuvenous Malformations (“Glomangiomas”) за авторством Pascal Brouillard, Laurence M. Boon, John B. Mulliken, O Enjolras, Michella Ghassibe‐Sabbagh, Matthew L. Warman, Oon Tian Tan, Bjørn R. Olsen, Miikka Vikkula
Опубліковано 2002Artigo -
3
Y-Chromosome and mtDNA Genetics Reveal Significant Contrasts in Affinities of Modern Middle Eastern Populations with European and African Populations за авторством Danielle A. Badro, Bouchra Douaihy, Marc Haber, Sonia Youhanna, Angelique K. Salloum, Michella Ghassibe‐Sabbagh, Brian Johnsrud, Georges Khazen, Elizabeth Matisoo‐Smith, David F. Soria‐Hernanz, R. Spencer Wells, Chris Tyler‐Smith, Daniel E. Platt, Pierre Zalloua
Опубліковано 2013Artigo -
4
Afghanistan's Ethnic Groups Share a Y-Chromosomal Heritage Structured by Historical Events за авторством Marc Haber, Daniel E. Platt, Maziar Ashrafian Bonab, Sonia Youhanna, David F. Soria‐Hernanz, Begoña Martínez‐Cruz, Bouchra Douaihy, Michella Ghassibe‐Sabbagh, Houshang Rafatpanah, Mohsen Ghanbari, John W. Whale, Oleg Balanovsky, R. Spencer Wells, David Comas, Chris Tyler‐Smith, Pierre Zalloua
Опубліковано 2012Artigo -
5
Large Scale Association Analysis Identifies Three Susceptibility Loci for Coronary Artery Disease за авторством Stephanie Saadé, Jean‐Baptiste Cazier, Michella Ghassibe‐Sabbagh, Sonia Youhanna, Danielle A. Badro, Yoichiro Kamatani, Jörg Hager, Joumana Yérétzian, Georges Khazen, Marc Haber, Angelique K. Salloum, Bouchra Douaihy, Raed Othman, Nabil Shasha, Samer Kabbani, Hamid el Bayeh, Elie Chammas, Martin Farrall, Dominique Gauguier, Daniel E. Platt, Pierre Zalloua
Опубліковано 2011Artigo -
6
Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis за авторством Jörg Hager, Yoichiro Kamatani, Jean‐Baptiste Cazier, Sonia Youhanna, Michella Ghassibe‐Sabbagh, Daniel E. Platt, Antoine Abchee, Jihane Romanos, Georges Khazen, Raed Othman, Danielle A. Badro, Marc Haber, Angelique K. Salloum, Bouchra Douaihy, Nabil Shasha, Samer Kabbani, Hana Sbeite, Elie Chammas, Hamid el Bayeh, Francis Rousseau, Diana Zélénika, Marta Gut, Mark Lathrop, Martin Farrall, Dominique Gauguier, Pierre Zalloua
Опубліковано 2012Artigo -
7
Prevalence and nonrandom distribution of exonic mutations in interferon regulatory factor 6 in 307 families with Van der Woude syndrome and 37 families with popliteal pterygium syn... за авторством Renata Lúcia Leite Ferreira de Lima, Sarah A. Hoper, Michella Ghassibe‐Sabbagh, Margaret E. Cooper, Nicholas K. Rorick, Shinji Kondo, Lori Katz, Mary L. Marazita, John G. Compton, Sherri J. Bale, Ute Hehr, Michael J. Dixon, Sandra Daack‐Hirsch, Odile Boute, Bénédicte Bayet, Nicole Revençu, Christine Verellen‐Dumoulin, Miikka Vikkula, Antônio Richieri‐Costa, Danilo Moretti‐Ferreira, Jeffrey C. Murray, Brian C. Schutte
Опубліковано 2009Artigo -
8
FAF1, a Gene that Is Disrupted in Cleft Palate and Has Conserved Function in Zebrafish за авторством Michella Ghassibe‐Sabbagh, Laurence Desmyter, Tobias Langenberg, Filip Claes, Odile Boute, Bénédicte Bayet, P. Pellerin, Karlien Hermans, Liesbeth Backx, M. Adela Mansilla, Sandra R. Imoehl, Stefanie Nowak, Kerstin U. Ludwig, Carlotta Baluardo, Melissa Ferrian, Peter Mossey, Markus M. Nöethen, Mieke Dewerchin, Geneviève François, Nicole Revençu, R Vanwijck, Jacqueline T. Hecht, Elisabeth Mangold, Jeffrey C. Murray, Michele Rubini, Joris Vermeesch, Hélène A. Poirel, Peter Carmeliet, Miikka Vikkula
Опубліковано 2011Artigo
Інструменти для пошуку:
Пов'язані теми
Biology
Gene
Genetics
Medicine
Population
Environmental health
Genotype
Archaeology
Computer science
Coronary artery disease
Craniofacial
Demography
Genetic association
Genome-wide association study
Geography
Haplotype
Interferon regulatory factors
Internal medicine
Middle East
Mutation
Pathology
Single-nucleotide polymorphism
Sociology
Transcription factor
Affinities
Afghan
Anatomy
Ancient history
Anthropology
Biochemistry