Facial morphometry of Ecuadorian patients with growth hormone receptor deficiency/Laron syndrome.

Por Schaefer, G B, Rosenbloom, A L, Guevara-Aguirre, J, Campbell, E A, Ullrich, F, Patil, K, Frias, J L
Publicado em 1994

Linkage of a human brain malformation, familial holoprosencephaly, to chromosome 7 and evidence for genetic heterogeneity.

Por Muenke, M, Gurrieri, F, Bay, C, Yi, D H, Collins, A L, Johnson, V P, Hennekam, R C, Schaefer, G B, Weik, L, Lubinsky, M S
Publicado em 1994