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Dalgleish, Raymond
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1

Re: Identification of a family with van der Hoeve's syndrom..:

Dalgleish, Raymond
Human Cell.  , 2024
Link: https://doi.org/10.1007/..
 
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2

Re: Long-term evaluation of anabolic and anti-resorptive ag..:

Dalgleish, Raymond
Osteoporosis International.  33 (2022)  6 - p. 1403-1404 , 2022
Link: https://doi.org/10.1007/..
 
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3

Dissecting the phenotypic variability of osteogenesis imper..:

Garibaldi, Nadia ; Besio, Roberta ; Dalgleish, Raymond...
Disease Models & Mechanisms.  15 (2022)  5 - p. , 2022
Link: https://doi.org/10.1242/..
 
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4

HUGO Gene Nomenclature Committee (HGNC) recommendations for..:

Bruford, Elspeth A. ; Antonescu, Cristina R. ; Carroll, Andrew J....
Leukemia.  35 (2021)  11 - p. 3040-3043 , 2021
Link: https://doi.org/10.1038/..
 
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5

A common classification framework for histone sequence alte..:

Leske, Henning ; Dalgleish, Raymond ; Lazar, Alexander J..
The Journal of Pathology.  254 (2021)  2 - p. 109-120 , 2021
Link: https://doi.org/10.1002/..
 
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6

EMQN best practice guidelines for genetic testing in dystro..:

Fratter, Carl ; Dalgleish, Raymond ; Allen, Stephanie K....
European Journal of Human Genetics.  28 (2020)  9 - p. 1141-1159 , 2020
Link: https://doi.org/10.1038/..
 
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7

Verifying nomenclature of DNA variants in submitted manuscr..:

Higgins, Jan ; Dalgleish, Raymond ; Dunnen, Johan T....
Human Mutation.  42 (2020)  1 - p. 3-7 , 2020
Link: https://doi.org/10.1002/..
 
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8

hgvs: A Python package for manipulating sequence variants u..:

Wang, Meng ; Callenberg, Keith M. ; Dalgleish, Raymond...
Human Mutation.  39 (2018)  12 - p. 1803-1813 , 2018
Link: https://doi.org/10.1002/..
 
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9

Mutations in COL1A1 Gene Change Dentin Nanostructure: A Res..:

Dalgleish, Raymond
The Anatomical Record.  301 (2018)  8 - p. 1307-1308 , 2018
Link: https://doi.org/10.1002/..
 
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10

VariantValidator: Accurate validation, mapping, and formatt..:

Freeman, Peter J. ; Hart, Reece K. ; Gretton, Liam J...
Human Mutation.  39 (2017)  1 - p. 61-68 , 2017
Link: https://doi.org/10.1002/..
 
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11

The collαgen III fibril has a "flexi-rod" structure of flex..:

Parkin, J. Des ; San Antonio, James D. ; Persikov, Anton V....
PLOS ONE.  12 (2017)  7 - p. e0175582 , 2017
Link: https://doi.org/10.1371/..
 
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12

HGVS Recommendations for the Description of Sequence Varian..:

den Dunnen, Johan T. ; Dalgleish, Raymond ; Maglott, Donna R....
Human Mutation.  37 (2016)  6 - p. 564-569 , 2016
Link: https://doi.org/10.1002/..
 
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13

LSDBs and How They Have Evolved: HUMAN MUTATION:

Dalgleish, Raymond
Human Mutation.  37 (2016)  6 - p. 532-539 , 2016
Link: https://doi.org/10.1002/..
 
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14

Cafe Variome: General-Purpose Software for Making Genotype-..:

Lancaster, Owen ; Beck, Tim ; Atlan, David...
Human Mutation.  36 (2015)  10 - p. 957-964 , 2015
Link: https://doi.org/10.1002/..
 
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15

Transcription factor SOHLH1 potentially associated with pri..:

Zhao, Shidou ; Li, Guangyu ; Dalgleish, Raymond...
Fertility and Sterility.  103 (2015)  2 - p. 548-553.e5 , 2015
Link: https://doi.org/10.1016/..
 
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