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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

98 related articles for article (PubMed ID: 10669209)

  • 1. Aggressive behavior in patients with Sotos syndrome.
    Mauceri L; Sorge G; Baieli S; Rizzo R; Pavone L; Coleman M
    Pediatr Neurol; 2000 Jan; 22(1):64-7. PubMed ID: 10669209
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Neuroradiologic findings in Sotos syndrome.
    Horikoshi H; Kato Z; Masuno M; Asano T; Nagase T; Yamagishi Y; Kozawa R; Arai T; Aoki M; Teramoto T; Omoya K; Matsumoto N; Kurotaki N; Shimokawa O; Kurosawa K; Kondo N
    J Child Neurol; 2006 Jul; 21(7):614-8. PubMed ID: 16970856
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Growth and development potpourri.
    Levitsky LL
    Curr Opin Endocrinol Diabetes Obes; 2012 Feb; 19(1):26-7. PubMed ID: 22157407
    [No Abstract]   [Full Text] [Related]  

  • 4. Further delineation of Weaver syndrome.
    Ardinger HH; Hanson JW; Harrod MJ; Cohen MM; Tibbles JA; Welch JP; Young-Wee T; Sommer A; Goldberg R; Shprintzen RJ
    J Pediatr; 1986 Feb; 108(2):228-35. PubMed ID: 2418189
    [TBL] [Abstract][Full Text] [Related]  

  • 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]  

  • 11. Cutis laxa with growth and developmental delay.
    Karakurt C; Sipahi T; Ceylaner S; Senocak F; Karademir S; Becer M
    Clin Pediatr (Phila); 2001 Jul; 40(7):422-3. PubMed ID: 11491141
    [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]  

  • 20. Developmental Foix-Chavany-Marie syndrome: polymicrogyria or macrogyria?
    Becker PS
    Ann Neurol; 1990 Jun; 27(6):693-4. PubMed ID: 1694420
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.