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Peters' anomaly and systemic defects.
van Schooneveld MJ, Delleman JW, Beemer FA, Bleeker-Wagemakers LM. van Schooneveld MJ, et al. Among authors: beemer fa. Arch Ophthalmol. 1986 Aug;104(8):1130. doi: 10.1001/archopht.1986.01050200036031. Arch Ophthalmol. 1986. PMID: 3741236 No abstract available.
Peters'-plus: a new syndrome.
van Schooneveld MJ, Delleman JW, Beemer FA, Bleeker-Wagemakers EM. van Schooneveld MJ, et al. Among authors: beemer fa. Ophthalmic Paediatr Genet. 1984 Dec;4(3):141-5. doi: 10.3109/13816818409006113. Ophthalmic Paediatr Genet. 1984. PMID: 6443615
Familial elastosis perforans serpiginosa.
Langeveld-Wildschut EG, Toonstra J, van Vloten WA, Beemer FA. Langeveld-Wildschut EG, et al. Among authors: beemer fa. Arch Dermatol. 1993 Feb;129(2):205-7. Arch Dermatol. 1993. PMID: 7679569
Oculocerebrocutaneous syndrome.
Bleeker-Wagemakers LM, Hamel BC, Hennekam RC, Beemer FA, Oorthuys HW. Bleeker-Wagemakers LM, et al. Among authors: beemer fa. J Med Genet. 1990 Jan;27(1):69-70. doi: 10.1136/jmg.27.1.69. J Med Genet. 1990. PMID: 2407849 Free PMC article. Review. No abstract available.
Overt cleft palate phenotype and TBX1 genotype correlations in velo-cardio-facial/DiGeorge/22q11.2 deletion syndrome patients.
Herman SB, Guo T, McGinn DM, Blonska A, Shanske AL, Bassett AS, Chow EW, Bowser M, Sheridan M, Beemer F, Devriendt K, Swillen A, Breckpot J, Digilio MC, Marino B, Dallapiccola B, Carpenter C, Zheng X, Johnson J, Chung J, Higgins AM, Philip N, Simon T, Coleman K, Heine-Suner D, Rosell J, Kates W, Devoto M, Zackai E, Wang T, Shprintzen R, Emanuel BS, Morrow BE; International Chromosome 22q11.2 Consortium. Herman SB, et al. Am J Med Genet A. 2012 Nov;158A(11):2781-7. doi: 10.1002/ajmg.a.35512. Epub 2012 Oct 3. Am J Med Genet A. 2012. PMID: 23034814 Free PMC article.
227 results