A. Monaco

Gene deletion causing adrenal hypoplasia congenita and hypogonadotrophic hypogonadism

A. Walker, G. Matfin, R. Sheaves, 1994, Clinical endocrinology.

Mutations and phenotype in isolated glycerol kinase deficiency.

J. Chelly, A. Walker, P. Willems, 1996, American journal of human genetics.

RECOMBINATION WITH PERT87 (DXS164) IN FAMILIES WITH X-LINKED MUSCULAR DYSTROPHY

M. Pericak-Vance, C. Bertelson, K. Fischbeck, 1986, The Lancet.

The chorea of McLeod syndrome

A. Monaco, A. Danek, M. Oechsner, 2001, Movement disorders : official journal of the Movement Disorder Society.

A novel point mutation in the mcleod syndrome gene in neuroacanthocytosis

A. Monaco, A. Harding, A. Harding, 1996, Annals of neurology.

Isolation and characterization of a MAGE gene family in the Xp21.3 region.

A. Monaco, A. Walker, F. Muscatelli, 1995, Proceedings of the National Academy of Sciences of the United States of America.

Northern epilepsy syndrome: an inherited childhood onset epilepsy with associated mental deterioration.

J. J. Shepherd, D. Sillence, L. Mestroni, 1994, Journal of medical genetics.