These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
31. Facio-cutaneous-skeletal syndrome is the Costello syndrome. Martin RA; Jones KL Am J Med Genet; 1993 Aug; 47(2):169, 73. PubMed ID: 8213899 [No Abstract] [Full Text] [Related]
32. Characteristic facial dysmorphism, arachnodactyly and mental handicap in two unrelated girls: a distinct MCA/MR syndrome? de Die-Smulders C; Vles H; Fryns JP Genet Couns; 1993; 4(2):165-7. PubMed ID: 8357568 [TBL] [Abstract][Full Text] [Related]
33. Further delineation of Costello syndrome. Teebi AS; Shaabani IS Am J Med Genet; 1993 Aug; 47(2):166-8. PubMed ID: 8213898 [TBL] [Abstract][Full Text] [Related]
34. Syndrome identification case report 93: unusual facies, hypotonia and constipation. Sondheimer JM J Clin Dysmorphol; 1983; 1(1):23-5. PubMed ID: 6580386 [No Abstract] [Full Text] [Related]
35. Costello or facio-cutaneous-skeletal syndrome? Teebi AS Am J Med Genet; 1993 Aug; 47(2):172-3; author reply 174. PubMed ID: 8213901 [No Abstract] [Full Text] [Related]
36. Hypotonic syndrome accompanied by paroxysmal paralyses and skew deviation. Havlová M; Otradovec J; Dittrich J Acta Univ Carol Med Monogr; 1976; (75):54-5. PubMed ID: 1088730 [No Abstract] [Full Text] [Related]
37. [Supravalvular aortic stenosis (Williams-Beuren syndrome). Report of a case]. de Oliveira Júnior W; Albuquerque MA; Albuquerque MA; Assi N; Moreira CR; de Melo Júnior MG; Lins M; Japiassu G; Papa R Arq Bras Cardiol; 1982 Dec; 39(6):399-404. PubMed ID: 7186395 [No Abstract] [Full Text] [Related]
39. [Cerebral gigantism (Sotos syndrome) in 7 Puerto Rican children]. Toro Solá M; Rivera Reyes L Bol Asoc Med P R; 1984 Apr; 76(4):146-50. PubMed ID: 6586192 [No Abstract] [Full Text] [Related]
40. Microcephaly, macrotia, unusual mimics and mental retardation syndrome: new syndrome or variant of De Lange type 2 syndrome. Verloes A; Lesenfants S; Philippet B; Iyawa A; Laloux F; Koulischer L Genet Couns; 1996; 7(4):277-82. PubMed ID: 8985731 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]