C. Kwok

Mutations in SOX9, the gene responsible for Campomelic dysplasia and autosomal sex reversal.

J. W. Foster, S. Mansour, O. Zuffardi, 1995, American journal of human genetics.

Evidence to exclude SOX9 as a candidate gene for XY sex reversal without skeletal malformation.

P. Goodfellow, J. Hawkins, C. Kwok, 1996, Journal of medical genetics.

Mutation analysis of the 2 kb 5' to SRY in XY females and XY intersex subjects.

C. Tyler-Smith, P. Goodfellow, I. Hughes, 1996, Journal of medical genetics.

Candidate genes in complete and partial XY sex reversal: Mutation analysis of SRY, SRY-related genes and FTZ-F1

I. Hughes, H. Lim, J. Hawkins, 1998, Molecular and Cellular Endocrinology.

females and XY intersex subjects . Mutation analysis of the 2 kb 5 ' to SRY in XY

C. Tyler-Smith, P. Goodfellow, I. Hughes, 2022 .

Campomelic dysplasia and autosomal sex reversal caused by mutations in an SRY-related gene

Sahar Mansour, Jean Weissenbach, J. Weissenbach, 1994, Nature.

A novel germ line mutation in SOX9 causes familial campomelic dysplasia and sex reversal.

D. Sillence, A. Sinclair, C. Cooke‐Yarborough, 1996, Human molecular genetics.

Campomelic Dysplasia with XY Sex Reversal: Diverse Phenotypes Resulting from Mutations in a Single Gene a

J. W. Foster, P. Goodfellow, A. J. Schafer, 1996, Annals of the New York Academy of Sciences.

The role of SOX9 in autosomal sex reversal and campomelic dysplasia.

J. Weissenbach, J. W. Foster, P. Goodfellow, 1995, Philosophical transactions of the Royal Society of London. Series B, Biological sciences.

Breakpoint break for consortium studying adult polycystic kidney disease

P. Goodfellow, Y. Ramkissoon, V. Wunderle, 1994, Cell.

Characterization of whole genome radiation hybrid mapping resources for non-mammalian vertebrates.

B. Paw, P. Goodfellow, D. Burt, 1998, Nucleic acids research.