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Raymond Dalgleish

Showing results (21-30 of 47) with videos related to

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Human Mutation|July 31, 2015
Cafe Variome: general-purpose software for making genotype-phenotype data discoverable in restricted or open access contextsOwen Lancaster, Tim Beck, David Atlan, et al.
European Journal of Human Genetics : EJHG|September 27, 2012
Clinical utility gene card for: osteogenesis imperfectaFleur S van Dijk, Raymond Dalgleish, Fransiska Malfait, et al.
Fertility and Sterility|February 15, 2014
Novel variants in the SOHLH2 gene are implicated in human premature ovarian failureYingying Qin, Xue Jiao, Raymond Dalgleish, et al.
Plos One|July 14, 2017
The collαgen III fibril has a "flexi-rod" structure of flexible sequences interspersed with rigid bioactive domains including two with hemostatic rolesJ Des Parkin, James D San Antonio, Anton V Persikov, et al.
Human Mutation|May 25, 2012
Solving bottlenecks in data sharing in the life sciencesRaymond Dalgleish, Eva Molero, Richard Kidd, et al.
European Journal of Human Genetics : EJHG|August 11, 2011
EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfectaFleur S van Dijk, Peter H Byers, Raymond Dalgleish, et al.
Human Mutation|January 7, 2010
The Human Variome Project (HVP) 2009 Forum "Towards Establishing Standards"Heather J Howard, Ourania Horaitis, Richard G H Cotton, et al.
Maturitas|October 10, 2013
Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: no association with premature ovarian failure (POF) in Serbian womenYingying Qin, Svetlana Vujovic, Guangyu Li, et al.
Nucleic Acids Research|November 29, 2013
Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variantsJacqueline A L MacArthur, Joannella Morales, Ray E Tully, et al.
Fertility and Sterility|December 21, 2014
Transcription factor SOHLH1 potentially associated with primary ovarian insufficiencyShidou Zhao, Guangyu Li, Raymond Dalgleish, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
Human Mutation|July 31, 2015
Cafe Variome: general-purpose software for making genotype-phenotype data discoverable in restricted or open access contextsOwen Lancaster, Tim Beck, David Atlan, et al.
European Journal of Human Genetics : EJHG|September 27, 2012
Clinical utility gene card for: osteogenesis imperfectaFleur S van Dijk, Raymond Dalgleish, Fransiska Malfait, et al.
Fertility and Sterility|February 15, 2014
Novel variants in the SOHLH2 gene are implicated in human premature ovarian failureYingying Qin, Xue Jiao, Raymond Dalgleish, et al.
Plos One|July 14, 2017
The collαgen III fibril has a "flexi-rod" structure of flexible sequences interspersed with rigid bioactive domains including two with hemostatic rolesJ Des Parkin, James D San Antonio, Anton V Persikov, et al.
Human Mutation|May 25, 2012
Solving bottlenecks in data sharing in the life sciencesRaymond Dalgleish, Eva Molero, Richard Kidd, et al.
European Journal of Human Genetics : EJHG|August 11, 2011
EMQN best practice guidelines for the laboratory diagnosis of osteogenesis imperfectaFleur S van Dijk, Peter H Byers, Raymond Dalgleish, et al.
Human Mutation|January 7, 2010
The Human Variome Project (HVP) 2009 Forum "Towards Establishing Standards"Heather J Howard, Ourania Horaitis, Richard G H Cotton, et al.
Maturitas|October 10, 2013
Ethnic specificity of variants of the ESR1, HK3, BRSK1 genes and the 8q22.3 locus: no association with premature ovarian failure (POF) in Serbian womenYingying Qin, Svetlana Vujovic, Guangyu Li, et al.
Nucleic Acids Research|November 29, 2013
Locus Reference Genomic: reference sequences for the reporting of clinically relevant sequence variantsJacqueline A L MacArthur, Joannella Morales, Ray E Tully, et al.
Fertility and Sterility|December 21, 2014
Transcription factor SOHLH1 potentially associated with primary ovarian insufficiencyShidou Zhao, Guangyu Li, Raymond Dalgleish, et al.
Pageof 5