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Tracy Dudding-Byth
66
results:
Search for persons
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Format
Online (66)
Mediatypes
Articles (Online) (26)
OpenAccess-fulltext (40)
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1
A systematic review and pooled analysis of penetrance estim..:
Goh, Shuxiang
;
Thiyagarajan, Lavvina
;
Dudding-Byth, Tracy
..
Genetics in Medicine. , 2024
Link:
https://doi.org/10.1016/..
?
2
A Genotype/Phenotype Study of KDM5B-Associated Disorders Su..:
Borroto, Maria Carla
;
Michaud, Coralie
;
Hudon, Chloé
...
Genes. 15 (2024) 8 - p. 1033 , 2024
Link:
https://doi.org/10.3390/..
?
3
How the Australian Functional Genomics Network (AFGN) contr..:
Scott, Hamish S.
;
Matotek, Ebony
;
Mattiske, Tessa
...
Pathology. 56 (2024) - p. S21-S22 , 2024
Link:
https://doi.org/10.1016/..
?
4
The ribose methylation enzyme FTSJ1 has a conserved role in..:
Brazane, Mira
;
Dimitrova, Dilyana G
;
Pigeon, Julien
...
Life Science Alliance. 6 (2023) 4 - p. e202201877 , 2023
Link:
https://doi.org/10.26508..
?
5
Methylation analysis and developmental profile of two indiv..:
Baker, Emma K.
;
Merton, Catherine F.
;
Tan, Wen-Hann
...
European Journal of Medical Genetics. 65 (2022) 4 - p. 104456 , 2022
Link:
https://doi.org/10.1016/..
?
6
Correction: The ARID1B spectrum in 143 patients: from nonsy..:
van der Sluijs, Pleuntje J.
;
Jansen, Sandra
;
Vergano, Samantha A.
...
Genetics in Medicine. 21 (2019) 9 - p. 2160-2161 , 2019
Link:
https://doi.org/10.1038/..
?
7
The ARID1B spectrum in 143 patients: from nonsyndromic inte..:
van der Sluijs, Pleuntje J.
;
Jansen, Sandra
;
Vergano, Samantha A.
...
Genetics in Medicine. 21 (2019) 6 - p. 1295-1307 , 2019
Link:
https://doi.org/10.1038/..
?
8
Enabling Global Clinical Collaborations on Identifiable Pat..:
Nellåker, Christoffer
;
Alkuraya, Fowzan S.
;
Baynam, Gareth
...
Frontiers in Genetics. 10 (2019) - p. , 2019
Link:
https://doi.org/10.3389/..
?
9
Significantly Elevated FMR1 mRNA and Mosaicism for Methylat..:
Field, Michael
;
Dudding-Byth, Tracy
;
Arpone, Marta
...
International Journal of Molecular Sciences. 20 (2019) 16 - p. 3907 , 2019
Link:
https://doi.org/10.3390/..
?
10
A recurrent missense variant inSLC9A7causes nonsyndromic X-..:
Khayat, Wujood
;
Hackett, Anna
;
Shaw, Marie
...
Human Molecular Genetics. 28 (2018) 4 - p. 598-614 , 2018
Link:
https://doi.org/10.1093/..
?
11
Computer face-matching technology using two-dimensional pho..:
Dudding-Byth, Tracy
;
Baxter, Anne
;
Holliday, Elizabeth G.
...
BMC Biotechnology. 17 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
?
12
Spinocerebellar ataxia type 29 due to mutations in ITPR1: a..:
Care4Rare Canada Consortium
;
Zambonin, Jessica L.
;
Bellomo, Allison
...
Orphanet Journal of Rare Diseases. 12 (2017) 1 - p. , 2017
Link:
https://doi.org/10.1186/..
?
13
Narrowing the critical region for overgrowth within 13q14.2..:
Kamien, Benjamin
;
Digilio, M. Cristina
;
Novelli, Antonio
...
European Journal of Medical Genetics. 58 (2015) 11 - p. 629-633 , 2015
Link:
https://doi.org/10.1016/..
?
14
Significantly Elevated FMR1 mRNA and Mosaicism for Methylat..:
Michael Field
;
Tracy Dudding-Byth
;
Marta Arpone
...
https://www.mdpi.com/1422-0067/20/16/3907. , 2019
Link:
https://doi.org/10.3390/..
?
15
Enabling Global Clinical Collaborations on Identifiable Pat..:
Christoffer Nellåker
;
Fowzan S. Alkuraya
;
Gareth Baynam
...
https://www.frontiersin.org/article/10.3389/fgene.2019.00611/full. , 2019
Link:
https://doi.org/10.3389/..
1-15