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1977 | 1 |
2021 | 1 |
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Eye and ocular adnexa manifestations of MED12-related disorders.
Ophthalmic Genet. 2022 Feb;43(1):126-129. doi: 10.1080/13816810.2021.1989601. Epub 2021 Oct 20.
Ophthalmic Genet. 2022.
PMID: 34670449
The FG syndrome: further characterization, report of a third family, and of a sporadic case.
Riccardi VM, Hässler E, Lubinsky MS.
Riccardi VM, et al.
Am J Med Genet. 1977;1(1):47-58. doi: 10.1002/ajmg.1320010106.
Am J Med Genet. 1977.
PMID: 565138
We report 5 new cases of the FG syndrome, 1 sporadic, 3 brothers from a European family, and another affected male born in the first FG syndrome family reported by Opitz and Kaveggia in 1974. ...
We report 5 new cases of the FG syndrome, 1 sporadic, 3 brothers from a European family, and another affected male born …
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