Publications by authors named "C Belgaid"

Claim this Profile
P
Point mutation in the helix termination peptide (HTP) of human type II hair keratin hHb6 causes monilethrix in five families.
B P Korge, E Healy, H Traupe, C Pünter, C Mauch, C E Belgaid

Exp Dermatol· August 1999

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Prognostic significance of allelic losses in primary melanoma.
E Healy, C Belgaid, M Takata, D Harrison, N W Zhu

Oncogene· April 1998

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mapping of monilethrix to the type II keratin gene cluster at chromosome 12q13 in three new families, including one with variable expressivity.
M A Birch-Machin, E Healy, R Turner, F Haldane, C E Belgaid

Br J Dermatol· September 1997

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Allelotypes of primary cutaneous melanoma and benign melanocytic nevi.
E Healy, C E Belgaid, M Takata, A Vahlquist, I Rehman

Cancer Res· February 1996

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13.
E Healy, S C Holmes, C E Belgaid, A M Stephenson, W H Mclean

Hum Mol Genet· December 1995

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis