D. Eteson

Syndrome of multiple pterygia, camptodactyly, facial anomalies, hypoplastic lungs and heart, cystic hygroma, and skeletal anomalies: delineation of a new entity and review of lethal forms of multiple pterygium syndrome.

J. Opitz, D. Rimoin, Harold Chen, 1984, American journal of medical genetics.

Pseudodiastrophic dysplasia: a distinct newborn skeletal dysplasia.

D. Rimoin, G. Beluffi, C. Belloni, 1986, The Journal of pediatrics.

DOOR syndrome (deafness, onycho-osteodystrophy, and mental retardation): a new patient and delineation of neurologic variability among recessive cases.

R. Lachman, E. Kakkis, H. J. Lin, 1993, American journal of medical genetics.

The role of mesenchyme-like tissue in the pathogenesis of thanatophoric dysplasia.

R. Burgeson, D. Rimoin, A. Ornoy, 1985, American journal of medical genetics.

Fibrochondrogenesis: radiologic and histologic studies.

D. Rimoin, P. Mastroiacovo, A. Ornoy, 1984, American journal of medical genetics.

Fragilitas ossium (fro/fro) in the mouse: a model for a recessively inherited type of osteogenesis imperfecta.

D. Sillence, H. Ritchie, T. Dibbayawan, 1993, American journal of medical genetics.