BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

183 related articles for article (PubMed ID: 16192740)

  • 1. Genetic analysis of tall stature.
    Kant SG; Wit JM; Breuning MH
    Horm Res; 2005; 64(3):149-56. PubMed ID: 16192740
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Clinical and molecular overlap in overgrowth syndromes.
    Baujat G; Rio M; Rossignol S; Sanlaville D; Lyonnet S; Le Merrer M; Munnich A; Gicquel C; Colleaux L; Cormier-Daire V
    Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):4-11. PubMed ID: 16010674
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Prenatal findings and the genetic diagnosis of fetal overgrowth disorders: Simpson-Golabi-Behmel syndrome, Sotos syndrome, and Beckwith-Wiedemann syndrome.
    Chen CP
    Taiwan J Obstet Gynecol; 2012 Jun; 51(2):186-91. PubMed ID: 22795092
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular basis of Sotos syndrome.
    Niikawa N
    Horm Res; 2004; 62 Suppl 3():60-5. PubMed ID: 15539801
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Tall stature in children and adolescents.
    Urakami T
    Minerva Pediatr; 2020 Dec; 72(6):472-483. PubMed ID: 32748612
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Two cases of Sotos syndrome with novel mutations of the NSD1 gene.
    Fryssira H; Drossatou P; Sklavou R; Barambouti F; Manolaki N
    Genet Couns; 2010; 21(1):53-9. PubMed ID: 20420030
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [Diagnosis and therapy of gigantism].
    Sorgo W; Teller WM
    Klin Padiatr; 1987; 199(2):63-9. PubMed ID: 3586561
    [TBL] [Abstract][Full Text] [Related]  

  • 10. NSD1 mutations in Sotos syndrome.
    Faravelli F
    Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):24-31. PubMed ID: 16010675
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Tall stature and duplication of the insulin-like growth factor I receptor gene.
    Kant SG; Kriek M; Walenkamp MJ; Hansson KB; van Rhijn A; Clayton-Smith J; Wit JM; Breuning MH
    Eur J Med Genet; 2007; 50(1):1-10. PubMed ID: 17056309
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. Psychosocial, cognitive, and motor functioning in patients with suspected Sotos syndrome: a comparison between patients with and without NSD1 gene alterations.
    de Boer L; Röder I; Wit JM
    Dev Med Child Neurol; 2006 Jul; 48(7):582-8. PubMed ID: 16780628
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Haploinsufficiency of NSD1 causes Sotos syndrome.
    Kurotaki N; Imaizumi K; Harada N; Masuno M; Kondoh T; Nagai T; Ohashi H; Naritomi K; Tsukahara M; Makita Y; Sugimoto T; Sonoda T; Hasegawa T; Chinen Y; Tomita Ha HA; Kinoshita A; Mizuguchi T; Yoshiura Ki K; Ohta T; Kishino T; Fukushima Y; Niikawa N; Matsumoto N
    Nat Genet; 2002 Apr; 30(4):365-6. PubMed ID: 11896389
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diagnosis of treatable types of short and tall stature.
    Zachmann M
    Postgrad Med J; 1978; 54 Suppl 1():121-32. PubMed ID: 364452
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. How to investigate a child with excessive growth?
    Coutant R; Donzeau A; Decrequy A; Louvigné M; Bouhours-Nouet N
    Ann Endocrinol (Paris); 2017 Jun; 78(2):98-103. PubMed ID: 28483364
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genotype-phenotype correlation in patients suspected of having Sotos syndrome.
    de Boer L; Kant SG; Karperien M; van Beers L; Tjon J; Vink GR; van Tol D; Dauwerse H; le Cessie S; Beemer FA; van der Burgt I; Hamel BC; Hennekam RC; Kuhnle U; Mathijssen IB; Veenstra-Knol HE; Stumpel CT; Breuning MH; Wit JM
    Horm Res; 2004; 62(4):197-207. PubMed ID: 15452385
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Exclusion of growth factor gene mutations as a common cause of Sotos syndrome.
    Lin AE; Liu Q; Mannheim GB; Darras BT
    Am J Med Genet; 2001 Jan; 98(1):101-2. PubMed ID: 11426446
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Three novel mutations in greek sotos patients with rare clinical manifestations.
    Leventopoulos G; Kitsiou-Tzeli S; Psoni S; Mavrou A; Kanavakis E; Willems P; Fryssira H
    Horm Res; 2009 Jan; 71(1):45-51. PubMed ID: 19039236
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.