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S.A. Wilcox
Observed names:
S WILCOX,
S. A. Wilcox,
SA Wilcox,
Stephen A Wilcox,
Stephen A. Wilcox
Observed institutions:
Royal Children's Hospital,
La Trobe University,
University of Otago
OpenAlex ID:
A5111956172
Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene
1997
·
F. Denoyelle
, D. Weil
, et al.
·
Human Molecular Genetics
·
633
PDF
Cloning and expression of a DAX1 homologue in the chicken embryo
2000
·
CA Smith
, V Clifford
, et al.
·
Journal of Molecular Endocrinology
·
67
PDF
Rapid isolation of recombinant lambda phage DNA for use in fluorescence in situ hybridization
1996
·
S. A. Wilcox
, R. Toder
, et al.
·
Chromosome Research
·
64
The human/mouse imprinted genesIGF2, H19, SNRPN andZNF127 map to two conserved autosomal clusters in a marsupial
1996
·
R. Toder
, S. A. Wilcox
, et al.
·
Chromosome Research
·
39
Statistical analysis of in situ hybridization data: Derivation and use of the Zmax test
1992
·
W.J. Ewens
, R.C. Griffiths
, et al.
·
Genomics
·
38
A Simple PCR Test to Detect the Common 35delG Mutation in the Connexin 26 Gene
2000
·
S WILCOX
, A OSBORN
, et al.
·
Molecular Diagnosis
·
26
SOX14 is a candidate gene for limb defects associated with BPES and Möbius syndrome
2000
·
H.P. Wilmore
, M.J. Smith
, et al.
·
Human Genetics
·
23
Connexin26 deafness in several interconnected families
1999
·
Stephen A Wilcox
, Amelia H Osborn
, et al.
·
Journal of Medical Genetics
·
19
Shared synteny between human chromosome 10 and chromosome 1 of the marsupial tammar wallaby, Macropus eugenii
2008
·
A.B. Spurdle
, P. Maccarone
, et al.
·
Cytogenetics and Cell Genetics
·
6
Subject Index, Vol. 77, 1997
2008
·
M. Schmid
, F. Saito-Ohara
, et al.
·
Cytogenetics and Cell Genetics
·
2
PDF
Biologically active composition of human W8B2( ) cardiac stem cell secretome
2017
·
Priyadharshini Sivakumaran
, Shuai Nie
, et al.
·
Human Gene Therapy
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Works count:
12
Citation count:
919
H-index:
8
I10-index:
8
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