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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.
Nucleic Acids Research|October 16, 2019
An improved platform for functional assessment of large protein libraries in mammalian cellsKenneth A Matreyek, Jason J Stephany, Melissa A Chiasson, et al.
American Journal of Medical Genetics. Part A|June 25, 2004
Perrault syndrome: evidence for progressive nervous system involvementAgata Fiumara, Giovanni Sorge, Antonio Toscano, et al.
American Journal of Medical Genetics. Part A|December 21, 2002
Documentation of anomalies not previously described in Fryns syndromeSonya Rae Arnold, Diane Debich-Spicer D, John M Opitz, et al.
Wiener Medizinische Wochenschrift (1946)|January 1, 1993
[Applied psychoacoustics in space flight]C Müller, P Schnider, A Persterer, 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.
Fetal and Pediatric Pathology|June 10, 2006
Segmentation anomalies of vertebrae and ribs with other abnormalities of blastogenesis: syndromes or associations?Enid Gilbert-Barness, Roelof-Jan Oostra, Archana Agarwal, et al.
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