Concepedia

Author

S.A. Wilcox

Royal Children's Hospital

Also Known As

S WILCOX, S Wilcox, S. A. Wilcox, S.A. Wilcox, SA Wilcox, Stephen A Wilcox, Wilcox, Stephen A.

13

Publications

913

Citations

8

H-Index

31

Concepts

All Affiliations

Royal Children's HospitalLa Trobe UniversityThe University of Melbourne
SW

About

S.A. Wilcox is an author at Royal Children's Hospital specializing in medicine, genetics, and molecular genetics.

Top Concepts

#ConceptH-IndexPublicationsCitations

1

Medicine

6

6

251

2

Molecular Biology

2

2

87

3

Public Health

1

1

38

4

Biostatistics

1

1

38

5

Cell Biology

1

1

67

S.A. Wilcox

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8

Publications

905

Citations

8

H-Index

YearCitations

Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene

Françoise Denoyelle, Dominique Weil, Marion A. Maw,

Human Molecular Genetics

1997

635

Cloning and expression of a DAX1 homologue in the chicken embryo

Vanessa Clifford, S.A. Wilcox, KS Bell

Journal of Molecular Endocrinology

2000

67

Rapid isolation of recombinant lambda phage DNA for use in fluorescence in situ hybridization

S.A. Wilcox, Roland Toder, Jamie W. Foster

Chromosome Research

1996

65

The human/mouse imprinted genesIGF2, H19, SNRPN andZNF127 map to two conserved autosomal clusters in a marsupial

Roland Toder, S.A. Wilcox, Megan Smithwick,

Chromosome Research

1996

39

Statistical analysis of in situ hybridization data: Derivation and use of the Zmax test

Warren J. Ewens, Robert Griffiths, S. N. Ethier,

Genomics

1992

38

A simple PCR test to detect the common 35delG mutation in the connexin 26 gene

S.A. Wilcox, Amelia H. Osborn, H H Dahl

Molecular Diagnosis

2000

22

SOX14 is a candidate gene for limb defects associated with BPES and M�bius syndrome

Helen P. Wilmore, Matthijs J. Smith, S.A. Wilcox,

Human Genetics

2000

20

Connexin26 deafness in several interconnected families

S.A. Wilcox, Amelia H. Osborn, D R Allen-Powell,

Journal of Medical Genetics

1999

19

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