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L C Wilson

Showing results (31-40 of 36) with videos related to

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Journal of Medical Genetics|June 3, 2004
Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypesM A Aldred, R O C Sanford, N S Thomas, et al.
Clinical Genetics|August 9, 2017
Bone health and SATB2-associated syndromeY A Zarate, M Steinraths, A Matthews, et al.
Journal of Medical Entomology|May 26, 2010
Test of recrudescence hypothesis for overwintering of West Nile virus in gray catbirdsJ C Owen, F R Moore, A J Williams, et al.
The Journal of Physiology|November 8, 2019
Global REACH 2018: The influence of acute and chronic hypoxia on cerebral haemodynamics and related functional outcomes during cold and heat stressT D Gibbons, M M Tymko, K N Thomas, et al.
Journal of Molecular Endocrinology|September 29, 2012
Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signallingD Hanson, P G Murray, T Coulson, et al.
Journal of Medical Genetics|June 28, 2006
A molecular and clinical study of Larsen syndrome caused by mutations in FLNBLouise S Bicknell, Claire Farrington-Rock, Yousef Shafeghati, et al.
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Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
Journal of Medical Genetics|June 3, 2004
Molecular analysis of 20 patients with 2q37.3 monosomy: definition of minimum deletion intervals for key phenotypesM A Aldred, R O C Sanford, N S Thomas, et al.
Clinical Genetics|August 9, 2017
Bone health and SATB2-associated syndromeY A Zarate, M Steinraths, A Matthews, et al.
Journal of Medical Entomology|May 26, 2010
Test of recrudescence hypothesis for overwintering of West Nile virus in gray catbirdsJ C Owen, F R Moore, A J Williams, et al.
The Journal of Physiology|November 8, 2019
Global REACH 2018: The influence of acute and chronic hypoxia on cerebral haemodynamics and related functional outcomes during cold and heat stressT D Gibbons, M M Tymko, K N Thomas, et al.
Journal of Molecular Endocrinology|September 29, 2012
Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signallingD Hanson, P G Murray, T Coulson, et al.
Journal of Medical Genetics|June 28, 2006
A molecular and clinical study of Larsen syndrome caused by mutations in FLNBLouise S Bicknell, Claire Farrington-Rock, Yousef Shafeghati, et al.
Pageof 4