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9. [Intra uterine major dwarfism with dysmorphia and severe encephalopathy. Bird head dwarfism (Virchow-Seckel type)]. Toudic L; Roche J; Alix D; Le Bars C; Dantoine G; Castel Y Ann Pediatr (Paris); 1977 Oct; 24(10):653-6. PubMed ID: 16211901 [No Abstract] [Full Text] [Related]
11. Seckel's dwarfism: analysis of chromosome breakage and sister chromatid exchanges. Cervenka J; Tsuchiya H; Ishiki T; Suzuki M; Mori H Am J Dis Child; 1979 May; 133(5):555-6. PubMed ID: 433882 [No Abstract] [Full Text] [Related]
12. [A new (brachymelic) type of primordial dwarfism (author's transl)]. Majewski F; Spranger J Monatsschr Kinderheilkd (1902); 1976 Jun; 124(6):499-503. PubMed ID: 934161 [TBL] [Abstract][Full Text] [Related]
13. Seckel syndrome: report of three sibships with the type I primordial dwarfism. Possible linkage with HLA locus. Stoppoloni G; Stabile M; Rinaldi MM; Prisco F; Rabuano RG; Pace E; Iafusco D; Stoppoloni F; Greco N Ann Genet; 1992; 35(4):213-6. PubMed ID: 1296517 [TBL] [Abstract][Full Text] [Related]
14. [Seckel syndrome: a case report]. Ortega MA; Infante-Velásquez EJ; Pérez del Campo YH Rev Neurol; 2002 Jul 1-15; 35(1):99-100. PubMed ID: 12389203 [No Abstract] [Full Text] [Related]
15. Seckel syndrome in a family with three affected children and hematological manifestations associated with chromosome instability. Syrrou M; Georgiou I; Paschopoulos M; Lolis D Genet Couns; 1995; 6(1):37-41. PubMed ID: 7794560 [TBL] [Abstract][Full Text] [Related]
16. Do some patients with Seckel syndrome have hematological problems and/or chromosome breakage? Butler MG; Hall BD; Maclean RN; Lozzio CB Am J Med Genet; 1987 Jul; 27(3):645-9. PubMed ID: 3115102 [TBL] [Abstract][Full Text] [Related]
17. Microcephaly, micrognathia, and bird-headed dwarfism: prenatal diagnosis of a Seckel-like syndrome. Majoor-Krakauer DF; Wladimiroff JW; Stewart PA; van de Harten JJ; Niermeijer MF Am J Med Genet; 1987 May; 27(1):183-8. PubMed ID: 3300331 [TBL] [Abstract][Full Text] [Related]
18. Osteodysplastic variant of primordial dwarfism. Shebib S; Hugosson C; Sakati N; Nyhan WL Am J Med Genet; 1991 Aug; 40(2):146-50. PubMed ID: 1897566 [TBL] [Abstract][Full Text] [Related]