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European Journal of Pediatrics|April 6, 1976
Studies of malformation syndromes of man XXXXIA: anatomical studies in the Hanhart syndrome--a pathogenetic hypothesisE T Bersu, J C Pettersen, W J Charboneau, et al.
American Journal of Medical Genetics|February 1, 1982
Phenotypic effects of inherited balanced translocationZ Ying, C Zaiyu, L Chunyun, et al.
American Journal of Medical Genetics|August 1, 1985
An X-linked recessive basal ganglia disorder with mental retardationR Laxova, E S Brown, K Hogan, et al.
Pediatrics|August 1, 1980
The MIller-Dieker syndromeK L Jones, E F Gilbert, E G Kaveggia, et al.
American Journal of Medical Genetics|January 1, 1979
The Johanson-Blizzard syndrome: case report and autopsy findingsD L Daentl, J L Frías, E F Gilbert, et al.
American Journal of Medical Genetics|July 27, 2001
Evidence for the "midline" hypothesis in associated defects of laterality formation and multiple midline anomaliesE Gilbert-Barness, D Debich-Spicer, M M Cohen, et al.
American Journal of Medical Genetics. Supplement|January 1, 1986
Two sporadic cases of amelia/phocomelia with similar phenotype: rare and unusually symmetrical form of FFU dysostosis or separate entity?N B Kardon, L P Dana, J M FitzGerald, et al.
European Journal of Pediatrics|March 18, 1977
Absence of spermatogonia in the Prader-Willi syndromeM L Katcher, G J Bargman, E F Gilbert, et al.
American Journal of Medical Genetics|October 1, 1993
Acrofacial dysostoses: review and report of a previously undescribed condition: the autosomal or X-linked dominant Catania form of acrofacial dysostosisJ M Opitz, F Mollica, G Sorge, et al.
American Journal of Medical Genetics|May 1, 1988
FG syndrome update 1988: note of 5 new patients and bibliographyJ M Opitz, A Richieri-da Costa, J M Aase, et al.
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