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White, SM
245
results:
Search for persons
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Format
Online (245)
Mediatypes
Articles (Online) (10)
OpenAccess-fulltext (235)
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1
Meeting the challenge of interpreting high‐resolution singl..:
Ganesamoorthy, D
;
Bruno, DL
;
McGillivray, G
...
BJOG: An International Journal of Obstetrics & Gynaecology. 120 (2013) 5 - p. 594-606 , 2013
Link:
https://doi.org/10.1111/..
?
2
PMH74 INTENSIVE COGNITIVE INTERVIEWING WITH PATIENTS DIAGNO..:
Bridges, JF
;
White, SM
Value in Health. 13 (2010) 3 - p. A118 , 2010
Link:
https://doi.org/10.1016/..
?
3
The clinical picture of the Börjeson–Forssman–Lehmann syndr..:
Turner, G
;
Lower, KM
;
White, SM
...
Clinical Genetics. 65 (2004) 3 - p. 226-232 , 2004
Link:
https://doi.org/10.1111/..
?
4
Principles of environmentally‐sustainable anaesthesia: a gl..:
White, SM
;
Shelton, CL
;
Gelb, AW
...
qt0cg8n80v. , 2022
Link:
https://escholarship.org..
?
5
Principles of environmentally-sustainable anaesthesia: a gl..:
White, SM
;
Shelton, CL
;
Gelb, AW
...
https://discovery.ucl.ac.uk/id/eprint/10172934/1/Principles%20of%20environmentally%20sustainable%20anaesthesia%20%20a%20global%20consensus%20statement.pdf. , 2022
Link:
https://discovery.ucl.ac..
?
6
Biallelic Variants in PYROXD2 Cause a Severe Infantile Meta..:
Van Bergen, NJ
;
Hock, DH
;
Spencer, L
...
issn:1422-0067. , 2022
Link:
http://hdl.handle.net/11..
?
7
De novo variants of CSNK2B cause a new intellectual disabil..:
Asif, M
;
Kaygusuz, E
;
Shinawi, M
...
issn:2666-2477. , 2022
Link:
http://hdl.handle.net/11..
?
8
Germline mutation in POLR2A: a heterogeneous, multi-systemi..:
Hansen, AW
;
Arora, P
;
Khayat, MM
...
issn:2666-2477. , 2021
Link:
http://hdl.handle.net/11..
?
9
Bi-allelic variants in IPO8 cause a connective tissue disor..:
Ziegler, A
;
Duclaux-Loras, R
;
Revenu, C
...
https://openaccess.sgul.ac.uk/id/eprint/113390/1/1-s2.0-S0002929721001518-main.pdf. , 2021
Link:
https://openaccess.sgul...
?
10
Principles of environmentally-sustainable anaesthesia: a gl..:
White, SM
;
Shelton, CL
;
Gelb, AW
...
issn:0003-2409. , 2021
Link:
http://hdl.handle.net/11..
?
11
Comprehensive study of 28 individuals with SIN3A-related di..:
Balasubramanian, M
;
Dingemans, AJM
;
Albaba, S
...
https://openaccess.sgul.ac.uk/id/eprint/113001/1/s41431-020-00769-7.pdf. , 2021
Link:
https://openaccess.sgul...
?
12
Bi-allelic variants in IPO8 cause a connective tissue disor..:
Ziegler, A
;
Duclaux-Loras, R
;
Revenu, C
...
issn:0002-9297. , 2021
Link:
http://hdl.handle.net/11..
?
13
Pathogenic variants in SMARCA5, a chromatin remodeler, caus..:
Li, D
;
Wang, Q
;
Gong, NN
...
issn:2375-2548. , 2021
Link:
http://hdl.handle.net/11..
?
14
Galactose treatment of a PGM1 patient presenting with restr..:
Donoghue, SE
;
White, SM
;
Tan, TY
...
issn:2192-8304. , 2021
Link:
http://hdl.handle.net/11..
?
15
Paediatric genomic testing: Navigating medicare rebatable g..:
Sachdev, R
;
Field, M
;
Baynam, GS
...
issn:1034-4810. , 2021
Link:
http://hdl.handle.net/11..
1-15