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Photo essay--Noonan syndrome.
Sommer A. Sommer A. Am J Med Genet C Semin Med Genet. 2007 Aug 15;145C(3):273. doi: 10.1002/ajmg.c.30147. Am J Med Genet C Semin Med Genet. 2007. PMID: 17640055 No abstract available.
12q14 microdeletion associated with HMGA2 gene disruption and growth restriction.
Alyaqoub F, Pyatt RE, Bailes A, Brock A, Deeg C, McKinney A, Astbury C, Reshmi S, Shane KP, Thrush DL, Sommer A, Gastier-Foster JM. Alyaqoub F, et al. Among authors: sommer a. Am J Med Genet A. 2012 Nov;158A(11):2925-30. doi: 10.1002/ajmg.a.35610. Epub 2012 Sep 14. Am J Med Genet A. 2012. PMID: 22987822
Craniofacial-deafness-hand syndrome revisited.
Sommer A, Bartholomew DW. Sommer A, et al. Am J Med Genet A. 2003 Nov 15;123A(1):91-4. doi: 10.1002/ajmg.a.20501. Am J Med Genet A. 2003. PMID: 14556253
In 1983 Sommer described a new syndrome in a mother and her infant daughter which was subsequently called the syndrome of craniofacial, hand anomalies and sensorineural deafness. The syndrome consisted of a normal calvarium with a flat facial pr …
In 1983 Sommer described a new syndrome in a mother and her infant daughter which was subsequently called the syndrome …
Photo essay--Seckel syndrome.
Sommer A. Sommer A. Am J Med Genet C Semin Med Genet. 2007 Aug 15;145C(3):230-1. doi: 10.1002/ajmg.c.30144. Am J Med Genet C Semin Med Genet. 2007. PMID: 17640052 No abstract available.
Familial occurrence of primary fibromyalgia.
Pellegrino MJ, Waylonis GW, Sommer A. Pellegrino MJ, et al. Among authors: sommer a. Arch Phys Med Rehabil. 1989 Jan;70(1):61-3. Arch Phys Med Rehabil. 1989. PMID: 2916922
1,129 results