Kết quả tìm kiếm - Raymond Dalgleish
- Đang hiển thị 1 - 18 kết quả của 18
-
1
Idiopathic acquired lacrimal drainage obstruction. Bằng Raymond Dalgleish
Được phát hành 1967Artigo -
2
The human type I collagen mutation database Bằng Raymond Dalgleish
Được phát hành 1997Artigo -
3
Mechanics and histology of senile entropion. Bằng Raymond Dalgleish, Judith Lee Smith
Được phát hành 1966Artigo -
4
Guidelines for establishing locus specific databases Bằng Mauno Vihinen, Johan T. den Dunnen, Raymond Dalgleish, Richard G.H. Cotton
Được phát hành 2011Artigo -
5
-
6
-
7
-
8
-
9
-
10
-
11
Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variants Bằng Jacqueline MacArthur, Joannella Morales, Ray Tully, Alex Astashyn, Laurent Gil, Elspeth A. Bruford, Pontus Larsson, Paul Flicek, Raymond Dalgleish, Donna Maglott, Fiona Cunningham
Được phát hành 2013Artigo -
12
HGVS Recommendations for the Description of Sequence Variants: 2016 Update Bằng 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
Được phát hành 2016Artigo -
13
Locus Reference Genomic sequences: an improved basis for describing human DNA variants Bằng 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
Được phát hành 2010Artigo -
14
HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions Bằng 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
Được phát hành 2021Artigo -
15
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... Bằng 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
Được phát hành 2006Revisão -
16
A corpus of GA4GH Phenopackets: case-level phenotyping for genomic diagnostics and discovery Bằng 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
Được phát hành 2024Pré-impressão -
17
A corpus of GA4GH phenopackets: case-level phenotyping for genomic diagnostics and discovery Bằng 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
Được phát hành 2024Artigo -
18
Planning the Human Variome Project: The Spain report Bằng 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
Được phát hành 2009Artigo
Công cụ tìm kiếm:
Các môn học liên quan
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