Isolation of the human Xp21 glycerol kinase gene by positional cloning. by Walker, A, Muscatelli, F, Monaco, A

ISOLATION OF CANDIDATE GENE(S) FOR ADRENOCORTICAL HYPOPLASIA-CONGENITA AND (OR) HYPOGONADOTROPIC HYPOGONADISM X-LINKED DISEASES by Muscatelli, F, Walker, A, Meitinger, T, Monaco, A

PHYSICAL AND GENETIC-MAPPING AND POSITIONAL CLONING OF DISEASE GENES IN XCEN-]Q21 by Chelly, J, Rider, S, Fairweather, N, Ishikawabrush, Y, Muscatelli, F, Monaco, A

Isolation and characterization of a MAGE gene family in the Xp21.3 region. by Muscatelli, F, Walker, A, De Plaen, E, Stafford, A, Monaco, A

Isolation of new probes from Xq12-->q13: an example of the screening of reference libraries with Alu-PCR products from radiation hybrids. by Muscatelli, F, Monaco, A, Goodfellow, P, Hors-Cayla, M, Lehrach, H, Fontes, M

PHYSICAL MAPPING AND POSITIONAL CLONING OF DISEASE GENES IN XP21 by Walker, A, Ho, M, Muscatelli, F, Chelly, J, Clarke, E, Ishikawabrush, Y, Monaco, A

Mutations in the DAX-1 gene give rise to both X-linked adrenal hypoplasia congenita and hypogonadotropic hypogonadism. by Muscatelli, F, Strom, T, Walker, A, Zanaria, E, Récan, D, Meindl, A, Bardoni, B, Guioli, S, Zehetner, G, Rabl, W

An unusual member of the nuclear hormone receptor superfamily responsible for X-linked adrenal hypoplasia congenita. by Zanaria, E, Muscatelli, F, Bardoni, B, Strom, T, Guioli, S, Guo, W, Lalli, E, Moser, C, Walker, A, McCabe, E

Two members of the human MAGEB gene family located in Xp21.3 are expressed in tumors of various histological origins. by Lurquin, C, De Smet, C, Brasseur, F, Muscatelli, F, Martelange, V, De Plaen, E, Brasseur, R, Monaco, A, Boon, T

Mutations and phenotype in isolated glycerol kinase deficiency. by Walker, A, Muscatelli, F, Stafford, A, Chelly, J, Dahl, N, Blomquist, H, Delanghe, J, Willems, P, Steinmann, B, Monaco, A