Результати пошуку - Sarah Servattalab
- Показ 1 - 6 результатів із 6
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1
Loss of PCLO function underlies pontocerebellar hypoplasia type III за авторством Momin Ahmed, Barry A. Chioza, Anna Rajab, Klaus Schmitz‐Abe, Aisha Al‐Khayat, Saeed Al-Turki, Emma L. Baple, Michael A. Patton, A. Al‐Memar, Matthew E. Hurles, Jennifer N. Partlow, Robert Hill, Gilad D. Evrony, Sarah Servattalab, Kyriacos Markianos, Christopher A. Walsh, Andrew H. Crosby, Ganeshwaran H. Mochida
Опубліковано 2015Artigo -
2
Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination за авторством Tojo Nakayama, Almundher Al‐Maawali, Malak El‐Quessny, Anna Rajab, Samir Khalil, Joan M. Stoler, Wen‐Hann Tan, Ramzi Nasir, Klaus Schmitz‐Abe, Robert Hill, Jennifer N. Partlow, Muna Al‐Saffar, Sarah Servattalab, Christopher M. LaCoursiere, Dimira Tambunan, Michael E. Coulter, Princess C. Elhosary, Grzegorz Górski, A. James Barkovich, Kyriacos Markianos, Annapurna Poduri, Ganeshwaran H. Mochida
Опубліковано 2015Artigo -
3
Socioeconomic and Racial and/or Ethnic Disparities in Multisystem Inflammatory Syndrome за авторством Karina Javalkar, Victoria Robson, Lukas K. Gaffney, Amy M. Bohling, Puneeta Arya, Sarah Servattalab, Jordan E. Roberts, Jeffrey I. Campbell, Sepehr Sekhavat, Jane W. Newburger, Sarah D. de Ferranti, Annette Baker, Pui Y. Lee, Megan Day‐Lewis, Emily M. Bucholz, Ryan Kobayashi, Mary Beth F. Son, Lauren A. Henderson, John N. Kheir, Kevin G. Friedman, Audrey Dionne
Опубліковано 2021Artigo -
4
Mutations in QARS, Encoding Glutaminyl-tRNA Synthetase, Cause Progressive Microcephaly, Cerebral-Cerebellar Atrophy, and Intractable Seizures за авторством Xiaochang Zhang, Jiqiang Ling, Giulia Barcia, Lili Jing, Jiang Wu, Brenda J. Barry, Ganeshwaran H. Mochida, R. Sean Hill, Jill M. Weimer, Quinn Stein, Annapurna Poduri, Jennifer N. Partlow, Dorothée Ville, Olivier Dulac, Timothy W. Yu, Anh-Thu N. Lam, Sarah Servattalab, Jacqueline Rodriguez, Nathalie Boddaert, Arnold Münnich, Laurence Colleaux, Leonard I. Zon, Dieter Söll, Christopher A. Walsh, Rima Nabbout
Опубліковано 2014Artigo -
5
Biallelic mutations in human DCC cause developmental split-brain syndrome за авторством Saumya Shekhar Jamuar, Klaus Schmitz‐Abe, Alissa M. D’Gama, Marie Drottar, Wai‐Man Chan, Maya Peeva, Sarah Servattalab, Anh-Thu N. Lam, Mauricio R. Delgado, Nancy J. Clegg, Zayed Al Zayed, Mohammad Asif Dogar, Ibrahim A. Alorainy, Abdullah Abu Jamea, Khaled K. Abu‐Amero, May L. Griebel, Wendy L. Ward, Ed S. Lein, Kyriacos Markianos, A. James Barkovich, Caroline D. Robson, P. Ellen Grant, Thomas M. Bosley, Elizabeth C. Engle, Christopher A. Walsh, Timothy W. Yu
Опубліковано 2017Artigo -
6
Somatic Mutations in Cerebral Cortical Malformations за авторством Saumya Shekhar Jamuar, Anh-Thu N. Lam, Martin Kircher, Alissa M. D’Gama, Jian Wang, Brenda J. Barry, Xiaochang Zhang, Robert Hill, Jennifer N. Partlow, Aldo Rozzo, Sarah Servattalab, Bhaven K. Mehta, Meral Topçu, Dina Amrom, Eva Andermann, Bernard Dan, Elena Parrini, Renzo Guerrini, Ingrid E. Scheffer, Samuel F. Berkovic, Richard J. Leventer, Yiping Shen, Bai Lin Wu, A. James Barkovich, Mustafa Şahin, Bernard S. Chang, Michael J. Bamshad, Deborah A. Nickerson, Jay Shendure, Annapurna Poduri, Timothy W. Yu, Christopher A. Walsh
Опубліковано 2014Artigo
Інструменти для пошуку:
Пов'язані теми
Biology
Gene
Genetics
Medicine
Neuroscience
Anatomy
Microcephaly
Mutation
Pathology
Phenotype
Agenesis of the corpus callosum
Anterior commissure
Anthropology
Atrophy
Body mass index
Brainstem
Commissure
Confidence interval
Corpus callosum
Demography
Disease
Environmental health
Ethnic group
Gene knockdown
Germline mutation
Haploinsufficiency
Hypoplasia
Intellectual disability
Internal medicine
Loss function