Որոնման արդյունքները - Raymond Dalgleish
- Ցուցադրվում են 1 - 18 արդյունքները 18
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Idiopathic acquired lacrimal drainage obstruction. Raymond Dalgleish
Հրապարակվել է 1967Artigo -
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The human type I collagen mutation database Raymond Dalgleish
Հրապարակվել է 1997Artigo -
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Mechanics and histology of senile entropion. Raymond Dalgleish, Judith Lee Smith
Հրապարակվել է 1966Artigo -
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EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfecta Fleur S van Dijk, Peter H. Byers, Raymond Dalgleish, Fransiska Malfait, Alessandra Maugeri, Marianne Rohrbach, Sofie Symoens, Erik A. Sistermans, Gerard Pals
Հրապարակվել է 2011Artigo -
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Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants Jacqueline MacArthur, Joannella Morales, Ray Tully, Alex Astashyn, Laurent Gil, Elspeth A. Bruford, Pontus Larsson, Paul Flicek, Raymond Dalgleish, Donna Maglott, Fiona Cunningham
Հրապարակվել է 2013Artigo -
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HGVS Recommendations for the Description of Sequence Variants: 2016 Update Johan T. den Dunnen, Raymond Dalgleish, Donna Maglott, Reece K. Hart, Marc S. Greenblatt, Jean McGowan‐Jordan, Anne‐Françoise Roux, Tim D. Smith, Stylianos E. Antonarakis, Peter E.M. Taschner
Հրապարակվել է 2016Artigo -
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Locus Reference Genomic sequences: an improved basis for describing human DNA variants Raymond Dalgleish, Paul Flicek, Fiona Cunningham, Alex Astashyn, Raymond E. Tully, Glenn Proctor, Yuan Chen, William McLaren, Pontus Larsson, Brendan Vaughan, Christophe Béroud, Glen Dobson, Heikki Lehväslaiho, Peter E.M. Taschner, Johan T. den Dunnen, A. Devereau, Ewan Birney, Anthony J. Brookes, Donna Maglott
Հրապարակվել է 2010Artigo -
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HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions Elspeth A. Bruford, Cristina R. Antonescu, Andrew J. Carroll, Arul M. Chinnaiyan, Ian A. Cree, Nicholas C.P. Cross, Raymond Dalgleish, Robert Peter Gale, Christine J. Harrison, Rosalind J. Hastings, Jean‐Loup Huret, Bertil Johansson, Michelle Le Beau, Cristina Mecucci, Fredrik Mertens, Roel G.W. Verhaak, Felix Mitelman
Հրապարակվել է 2021Artigo -
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Consortium for osteogenesis imperfecta mutations in the helical domain of type I collagen: regions rich in lethal mutations align with collagen binding sites for integrins and prot... Joan C. Marini, Antonella Forlino, Wayne A. Cabral, Aileen M. Barnes, James D. San Antonio, Sarah A. Milgrom, James Hyland, Jarmo Körkkö, Darwin J. Prockop, Anne De Paepe, Paul Coucke, Sofie Symoens, Francis H. Glorieux, Peter J. Roughley, Allan M. Lund, Kaija Kuurila-Svahn, Heini Hartikka, Daniel H. Cohn, Deborah Krakow, Monica Mottes, Ulrike Schwarze, Diana Chen, Kathleen Yang, Christine Kuslich, James Troendle, Raymond Dalgleish, Peter H. Byers
Հրապարակվել է 2006Revisão -
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A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discovery Daniel Daniš, Michael J Bamshad, Yasemin Bridges, Pilar Cacheiro, Leigh Carmody, Jessica X. Chong, Ben Coleman, Raymond Dalgleish, Peter Freeman, Adam S.L. Graefe, Tudor Groza, Julius O.B. Jacobsen, Adam Klocperk, Maaike Kusters, Markus S. Ladewig, Anthony J. Marcello, Teresa Mattina, Chris Mungall, Monica Muñoz‐Torres, Justin Reese, Filip Rehburg, Bárbara Carvalho Santos dos Reis, Catharina Schuetz, Damian Smedley, Timmy Strauß, Jagadish Chandrabose Sundaramurthi, Sylvia Thun, Kyran Wissink, J. Wagstaff, David Zocche, Melissa Haendel, Peter N. Robinson
Հրապարակվել է 2024Pré-impressão -
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A corpus of GA4GH phenopackets: case-level phenotyping for genomic diagnostics and discovery Daniel Daniš, Michael J Bamshad, Yasemin Bridges, Andrés Caballero-Oteyza, Pilar Cacheiro, Leigh Carmody, Leonardo Chimirri, Jessica X. Chong, Ben Coleman, Raymond Dalgleish, Peter Freeman, Adam S.L. Graefe, Tudor Groza, Peter Hansen, Julius O.B. Jacobsen, Adam Klocperk, Maaike Kusters, Markus S. Ladewig, Anthony J. Marcello, Teresa Mattina, Chris Mungall, Monica C. Munoz-Torres, Justin Reese, Filip Rehburg, Bárbara Carvalho Santos dos Reis, Catharina Schuetz, Damian Smedley, Timmy Strauß, Jagadish Chandrabose Sundaramurthi, Sylvia Thun, Kyran Wissink, J. Wagstaff, David Zocche, Melissa Haendel, Peter N. Robinson
Հրապարակվել է 2024Artigo -
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Planning the Human Variome Project: The Spain report Jim Kaput, Richard G.H. Cotton, L Hardman, Michael S. Watson, Aida I. Al Aqeel, Jumana Y. Al‐Aama, Fahd Al‐Mulla, Santos Alonso, Stefan Aretz, Arleen D. Auerbach, Bharati Bapat, Inge Bernstein, Jong Bhak, Stacey Bléoo, Helmut Blöcker, Steven E. Brenner, John Burn, Mariona Bustamante, Rita Calzone, Anne Cambon‐Thomsen, Michele Cargill, Paola Carrera, Lawrence Cavedon, Yoon Shin Cho, Yeun‐Jun Chung, Mireille Claustres, Garry R. Cutting, Raymond Dalgleish, Johan T. den Dunnen, Carlos Bustamante, Steven F. Dobrowolski, Rosário Santos, Rosemary Ekong, Simon B. Flanagan, Paul Flicek, Yoichi Furukawa, Maurizio Genuardi, Ho Ghang, М. В. Голубенко, Marc S. Greenblatt, Ada Hamosh, John M. Hancock, Ross C. Hardison, Terence Harrison, Robert Hoffmann, Rania Horaitis, Heather J. Howard, Carol Isaacson Barash, Neskuts Izagirre, Jongsun Jung, Toshio Kojima, Sandrine Laradi, Yeon-Su Lee, Jong‐Young Lee, Vera Lúcia Gil‐da‐Silva‐Lopes, Finlay Macrae, Donna Maglott, Makia J. Marafie, Steven G. E. Marsh, Yoichi Matsubara, Ludwine M. Messiaen, Gabriela Möslein, Mihai G. Netea, Melissa Norton, Peter J. Oefner, William S. Oetting, James O’Leary, Ana María Oller Ramírez, Mark H. Paalman, Jillian S. Parboosingh, George P. Patrinos, Giuditta Perozzi, Ian Phillips, Sue Povey, S Prasad, Ming Qi, David J. Quin, Raj Ramesar, C. Sue Richards, Judy Savige, D. Scheible, Rodney J. Scott, Daniela Seminara, Elizabeth A. Shephard, Rolf H. Sijmons, Tim D. Smith, María-Jesús Sobrido, Toshihiro Tanaka, Sean V. Tavtigian, Graham R. Taylor, Jon W. Teague, Thoralf Töpel, Mollie Ullman-Culleré, Joji Utsunomiya, Henk J. van Kranen, Mauno Vihinen, Elizabeth Webb, Thomas K. Weber, Meredith Yeager, Young Il Yeom
Հրապարակվել է 2009Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Biology
Genetics
Gene
Computational biology
Genome
Computer science
Medicine
Data science
Human genome
Genomics
Osteogenesis imperfecta
Pathology
Anatomy
Endocrinology
Exon
Programming language
Reference genome
Bioinformatics
DNA sequencing
Data mining
Extracellular matrix
Gene nomenclature
Human genetics
Internal medicine
Law
Locus (genetics)
Molecular biology
Mutation
Nomenclature
Political science