Výsledky vyhledávání - B S Emanuel
- Zobrazuji výsledky 1 - 10 z 10
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Human histone genes map to multiple chromosomes. Autor P. Tripputi, B S Emanuel, C M Croce, L Green, Gary S. Stein, Janet L. Stein
Vydáno 1986Artigo -
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EWS-erg and EWS-Fli1 fusion transcripts in Ewing's sarcoma and primitive neuroectodermal tumors with variant translocations. Autor Marco Giovannini, Jaclyn A. Biegel, Massimo Serra, J.Y. Wang, Yau‐Huei Wei, Lynn M. Nycum, B S Emanuel, Gerald A. Evans
Vydáno 1994Artigo -
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Chromosomal localization of the genes for the vitronectin and fibronectin receptors alpha subunits and for platelet glycoproteins IIb and IIIa. Autor Donna M. Sosnoski, B S Emanuel, Anita L. Hawkins, Peter van Tuinen, David H. Ledbetter, Robert L. Nussbaum, F T Kaos, Elias Schwartz, David R. Phillips, Joel Bennett
Vydáno 1988Artigo -
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A neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium Autor Raquel E. Gur, Anne S. Bassett, Donna M. McDonald‐McGinn, Carrie E. Bearden, Eva W.C. Chow, B S Emanuel, Michael J. Owen, Ann Swillen, Marianne B. M. van den Bree, Joris Vermeesch, J.A.S. Vorstman, Stephen T. Warren, Thomas Lehner, Bernice E. Morrow
Vydáno 2017Artigo -
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Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion Autor Isabelle Cleynen, Worrawat Engchuan, Matthew S. Hestand, Tracy Heung, Aaron M. Holleman, H. Richard Johnston, Thomas Monfeuga, Donna M. McDonald‐McGinn, Raquel E. Gur, Bernice E. Morrow, Ann Swillen, Jacob Vorstman, Carrie E. Bearden, Eva W. C. Chow, Marianne B. M. van den Bree, B S Emanuel, Joris Vermeesch, Stephen T. Warren, Michael J. Owen, Pankaj Chopra, David J. Cutler, Richard Duncan, Alex Kotlar, Jennifer G. Mulle, Anna J. Voss, Michael E. Zwick, Alexander Diacou, Aaron Golden, Tingwei Guo, Jhih-Rong Lin, Tao Wang, Zhengdong Zhang, Yingjie Zhao, Christian R. Marshall, Daniele Merico, Andrea Jin, Brenna Lilley, Harold I. Salmons, Oanh Tran, Peter Holmans, Antonio F. Pardiñas, James Walters, Wolfram Demaerel, Erik Boot, Nancy J. Butcher, Gregory Costain, Chelsea Lowther, Rens Evers, Thérèse van Amelsvoort, Esther van Duin, Claudia Vingerhoets, Jeroen Breckpot, Koenraad Devriendt, Elfi Vergaelen, Annick Vogels, T. Blaine Crowley, Daniel E. McGinn, Edward Moss, Robert Sharkus, Marta Unolt, Elaine H. Zackai, Monica E. Calkins, Robert S. Gallagher, Ruben C. Gur, Sunny X. Tang, Rosemarie Fritsch, Claudia Ornstein, Gabriela M. Repetto, Elemi Breetvelt, Sasja N. Duijff, Ania Fiksinski, Hayley Moss, Maria Niarchou, Kieran C. Murphy, Sarah E. Prasad, Eileen Daly, Maria Gudbrandsen, Clodagh M. Murphy, Declan Murphy, Antonio Buzzanca, Fabio Di Fabio, Maria Cristina Digilio, Maria Pontillo, Bruno Marino, Stefano Vicari, Karlene Coleman, Joseph F. Cubells, Opal Ousley, Miri Carmel, Doron Gothelf, Ehud Mekori‐Domachevsky, Elena Michaelovsky, Ronnie Weinberger, Abraham Weizman, Leila Kushan, Maria Jalbrzikowski, Marco Armando, Stéphan Eliez, Corrado Sandini, Maude Schneider
Vydáno 2020Artigo
Vyhledávací nástroje:
Související témata
Biology
Gene
Genetics
Molecular biology
Chromosome
Medicine
Chromosomal translocation
Chromosome 22
DiGeorge syndrome
ABL
Autosome
Breakpoint
Cancer research
Chronic myelogenous leukemia
Copy-number variation
Deletion syndrome
Environmental health
Fluorescence in situ hybridization
Genome
Genome-wide association study
Genotype
Karyotype
Leukemia
Pathology
Phenotype
Philadelphia chromosome
Population
Psychiatry
Psychology
Psychosis