Ngā hua rapu - Martin J. Somerville
- E whakaatu ana i te 1 - 7 hua o te 7
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1
GDF6, a Novel Locus for a Spectrum of Ocular Developmental Anomalies mā Mika Asai-Coakwell, Curtis R. French, K. Berry, Ming Ye, Ron Koss, Martin J. Somerville, Rosemary Mueller, Veronica van Heyningen, Andrew J. Waskiewicz, Ordan J. Lehmann
I whakaputaina 2007Artigo -
2
Chromosome 1q21.1 Contiguous Gene Deletion Is Associated With Congenital Heart Disease mā Jesse Christiansen, John D. Dyck, Basil G. Elyas, Margaret Lilley, J. Bamforth, Mark Hicks, Kathleen A. Sprysak, Robert Tomaszewski, Shelagh Haase, Leanne M. Vicen-Wyhony, Martin J. Somerville
I whakaputaina 2004Artigo -
3
Identification of copy number variants in miscarriages from couples with idiopathic recurrent pregnancy loss mā Evica Rajcan‐Separovic, Dan Diego‐Álvarez, Wendy P. Robinson, Christine Tyson, Ying Qiao, Chansonette Harvard, Chris Fawcett, Dagmar K. Kalousek, Tom Philipp, Martin J. Somerville, Mary D. Stephenson
I whakaputaina 2010Artigo -
4
Severe Expressive-Language Delay Related to Duplication of the Williams–Beuren Locus mā Martin J. Somerville, Carolyn Β. Mervis, Edwin J. Young, Eul‐Ju Seo, Miguel Del Campo, Stephen Bamforth, Ella Peregrine, Wayne Loo, Margaret Lilley, Luis A. Pérez‐Jurado, Colleen A. Morris, Stephen W. Scherer, Lucy R. Osborne
I whakaputaina 2005Artigo -
5
Microduplication and Triplication of 22q11.2: A Highly Variable Syndrome mā Twila M. Yobb, Martin J. Somerville, Lionel Willatt, Helen V. Firth, Karen J. Harrison, Jennifer MacKenzie, Natasha Gallo, Bernice E. Morrow, Lisa G. Shaffer, Melanie Babcock, Judy Chernos, François Bernier, Kathy Sprysak, Jesse Christiansen, Shelagh Haase, Basil G. Elyas, Margaret Lilley, Steven Bamforth, Heather E. McDermid
I whakaputaina 2005Artigo -
6
Global variation in copy number in the human genome mā Richard Redon, Shumpei Ishikawa, Karen Fitch, Lars Feuk, George H. Perry, T. Daniel Andrews, Heike Fiegler, Michael H. Shapero, Andrew R. Carson, Wei‐Wen Chen, Eun Kyung Cho, Stephanie Dallaire, Jennifer L. Freeman, Juan R. González, Mónica Gratacòs, Jing Huang, Dimitrios Rafail Kalaitzopoulos, Daisuke Komura, Jeffrey R. MacDonald, Christian R. Marshall, Rui Mei, Lyndal Montgomery, Kunihiro Nishimura, K. Okamura, Fan Shen, Martin J. Somerville, Joëlle Tchinda, Armand Valsesia, Cara Woodwark, Fengtang Yang, Junjun Zhang, Tatiana Zerjal, Jane Zhang, Lluı́s Armengol, Donald F. Conrad, Xavier Estivill, Chris Tyler‐Smith, Nigel P. Carter, Hiroyuki Aburatani, Charles Lee, Keith Jones, Stephen W. Scherer, Matthew E. Hurles
I whakaputaina 2006Artigo -
7
The clinical utility of integrative genomics in childhood cancer extends beyond targetable mutations mā Anita Villani, Scott Davidson, Nisha Kanwar, Winnie Lo, Yisu Li, Sarah Cohen‐Gogo, Fabio Fuligni, Lisa-Monique Edward, Nicholas Light, Mehdi Layeghifard, Ricardo Harripaul, Larissa Waldman, Bailey Gallinger, Federico Comitani, Ledia Brunga, Reid Hayes, Nathaniel D. Anderson, Arun Ramani, Kyoko E. Yuki, Sasha Blay, Brittney Johnstone, Cara Inglese, Rawan Hammad, Catherine Goudie, Andrew Y. Shuen, Jonathan D. Wasserman, Rosemarie E. Venier, Marianne Eliou, Miranda Lorenti, Carol Ann Ryan, Michael Braga, Meagan Gloven-Brown, Jianan Han, P. Montero, Famida Spatare, James A. Whitlock, Stephen W. Scherer, Kathy Chun, Martin J. Somerville, Cynthia Hawkins, Mohamed Abdelhaleem, Vijay Ramaswamy, Gino R. Somers, Lianna Kyriakopoulou, Johann Hitzler, Mary Shago, Daniel A. Morgenstern, Uri Tabori, M. Stephen Meyn, Meredith S. Irwin, David Malkin, Adam Shlien
I whakaputaina 2022Artigo
Ngā utauta rapu:
Ngā marau whai pānga
Biology
Gene
Genetics
Medicine
Genome
Phenotype
Chromosome
Computational biology
Copy-number variation
Gene duplication
Locus (genetics)
Mutation
Pathology
Anophthalmia
Bioinformatics
Botany
Cancer
Cardiology
Childhood cancer
Chromosomal rearrangement
Cognition
Cohort
Coloboma
Comparative genomic hybridization
Deletion syndrome
Disease
Eye development
Fragile X syndrome
Gene deletion
Genomics