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5. Sacrococcygeal teratoma in two cases of Sotos syndrome. Leonard NJ; Cole T; Bhargava R; Honoré LH; Watt J Am J Med Genet; 2000 Nov; 95(2):182-4. PubMed ID: 11078573 [No Abstract] [Full Text] [Related]
6. Diagnosing Sotos syndrome in the setting of global developmental delay and macrocephaly. Srour M; Mazer B; Shevell MI J Child Neurol; 2006 Apr; 21(4):287-90. PubMed ID: 16900922 [TBL] [Abstract][Full Text] [Related]
7. Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes. Türkmen S; Gillessen-Kaesbach G; Meinecke P; Albrecht B; Neumann LM; Hesse V; Palanduz S; Balg S; Majewski F; Fuchs S; Zschieschang P; Greiwe M; Mennicke K; Kreuz FR; Dehmel HJ; Rodeck B; Kunze J; Tinschert S; Mundlos S; Horn D Eur J Hum Genet; 2003 Nov; 11(11):858-65. PubMed ID: 14571271 [TBL] [Abstract][Full Text] [Related]
8. Spectrum of NSD1 gene mutations in southern Chinese patients with Sotos syndrome. Tong TM; Hau EW; Lo IF; Chan DH; Lam ST Chin Med J (Engl); 2005 Sep; 118(18):1499-506. PubMed ID: 16232326 [TBL] [Abstract][Full Text] [Related]
9. Spectrum of NSD1 mutations in Sotos and Weaver syndromes. Rio M; Clech L; Amiel J; Faivre L; Lyonnet S; Le Merrer M; Odent S; Lacombe D; Edery P; Brauner R; Raoul O; Gosset P; Prieur M; Vekemans M; Munnich A; Colleaux L; Cormier-Daire V J Med Genet; 2003 Jun; 40(6):436-40. PubMed ID: 12807965 [TBL] [Abstract][Full Text] [Related]
10. Dysmorphism, variable overgrowth, normal bone age, and severe developmental delay: a "Sotos-like" syndrome? Amiel J; Faivre L; Wilson L; Le Merrer M; Munnich A; Winter R; Lyonnet S; Cormier-Daire V J Med Genet; 2002 Feb; 39(2):148-52. PubMed ID: 11836369 [No Abstract] [Full Text] [Related]
12. MLPA analysis in 30 Sotos syndrome patients revealed one total NSD1 deletion and two partial deletions not previously reported. Fagali C; Kok F; Nicola P; Kim C; Bertola D; Albano L; Koiffmann CP Eur J Med Genet; 2009; 52(5):333-6. PubMed ID: 19596467 [TBL] [Abstract][Full Text] [Related]
13. Behavioural and emotional characteristics in children with Sotos syndrome and learning disabilities. Sarimski K Dev Med Child Neurol; 2003 Mar; 45(3):172-8. PubMed ID: 12613773 [TBL] [Abstract][Full Text] [Related]
14. [Hypotrophy in infants due to emotional deprivation. Study of 18 cases]. Ollivier A; Rapoport D; Etevenaux J; Guilhaume A; Richardet JM Ann Pediatr (Paris); 1983 Apr; 30(4):263-9. PubMed ID: 6190425 [No Abstract] [Full Text] [Related]
15. Lymphoproliferative disorders in Sotos syndrome: observation of two cases. Corsello G; Giuffrè M; Carcione A; Cuzto ML; Piccione M; Ziino O Am J Med Genet; 1996 Sep; 64(4):588-93. PubMed ID: 8870927 [TBL] [Abstract][Full Text] [Related]
16. Reply to "lymphoproliferative disorders in Sotos syndrome: observation in two cases". Cole T; Allanson J Am J Med Genet; 1998 Jan; 75(2):226-7. PubMed ID: 9450893 [No Abstract] [Full Text] [Related]
17. The syndromes of Sotos and Weaver: reports and review. Opitz JM; Weaver DW; Reynolds JF Am J Med Genet; 1998 Oct; 79(4):294-304. PubMed ID: 9781911 [TBL] [Abstract][Full Text] [Related]
18. Combined immunodeficiency, facial dysmorphism, optic nerve atrophy, skeletal anomalies and developmental delay: a new syndrome. Roifman CM; Chitayat D Clin Genet; 2009 Nov; 76(5):449-57. PubMed ID: 19863561 [TBL] [Abstract][Full Text] [Related]
19. Sotos syndrome: a study of the diagnostic criteria and natural history. Cole TR; Hughes HE J Med Genet; 1994 Jan; 31(1):20-32. PubMed ID: 7512144 [TBL] [Abstract][Full Text] [Related]