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William Halliday
Observed names:
W Halliday,
W. Halliday,
W.H. Halliday
Observed institutions:
Mount Sinai Hospital,
University Health Network,
University of Toronto,
Toronto Western Hospital,
Hospital for Sick Children,
University of Manitoba
show all 6
OpenAlex ID:
A5110071483
Missense mutations in β-1,3-N-acetylglucosaminyltransferase 1 (B3GNT1) cause Walker–Warburg syndrome
2013
·
Karen Buysse
, Moniek Riemersma
, et al.
·
Human Molecular Genetics
·
144
PDF
The Degree of Facial Movement following Microvascular Muscle Transfer in Pediatric Facial Reanimation Depends on Donor Motor Nerve Axonal Density
2015
·
Alison K. Snyder-Warwick
, Adel Y. Fattah
, et al.
·
Plastic & Reconstructive Surgery
·
124
Limb-girdle muscular dystrophy and Miyoshi myopathy in an aboriginal Canadian kindred map to LGMD2B and segregate with the same haplotype.
1996
·
T Weiler
, C R Greenberg
, et al.
·
PubMed
·
88
Complex V TMEM70 deficiency results in mitochondrial nucleoid disorganization
2010
·
Jessie M. Cameron
, Valeriy Levandovskiy
, et al.
·
Mitochondrion
·
47
Cerebellar Endometriosis
2004
·
Dipanka Sarma
, Pratibha Iyengar
, et al.
·
American Journal of Roentgenology
·
44
Limb girdle muscular dystrophy in Manitoba Hutterites does not map to any of the known LGMD loci
1997
·
Tracey Weiler
, Cheryl R. Greenberg
, et al.
·
American Journal of Medical Genetics
·
17
G.P.47
2014
·
N. Chrestian
, J. Dowling
, et al.
·
Neuromuscular Disorders
Genetic analysis in a variant of limb girdle muscular dystrophy in an inbred aboriginal community
1994
·
C. R. Greenberg
, Edward Nylen
, et al.
·
The American Journal of Human Genetics
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Works count:
8
Citation count:
464
H-index:
6
I10-index:
6
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