BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

226 related articles for article (PubMed ID: 10570915)

  • 1. Prader-Willi syndrome in a child with XYY.
    Honma A; Ishii R; Ito A; Kato M; Saitoh S; Hayasaka K
    J Hum Genet; 1999; 44(6):412-3. PubMed ID: 10570915
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular diagnosis of Prader-Willi syndrome.
    Pangkanon S
    J Med Assoc Thai; 2003 Aug; 86 Suppl 3():S510-6. PubMed ID: 14700141
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Sporadic occurrence of nondeletion Prader-Willi syndrome in two cases: a female with maternal uniparental disomy and a male with complex chromosomal rearrangement.
    Murthy SK; al-Nassar KE; Verghese L
    Nutrition; 1995; 11(5 Suppl):650-2. PubMed ID: 8748243
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The contribution of uniparental disomy to congenital development defects in children born to mothers at advanced childbearing age.
    Ginsburg C; Fokstuen S; Schinzel A
    Am J Med Genet; 2000 Dec; 95(5):454-60. PubMed ID: 11146466
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.
    Calounova G; Novotna D; Simandlova M; Havlovicova M; Zumrová A; Kocarek E; Sedlacek Z
    Neuro Endocrinol Lett; 2006 Oct; 27(5):579-85. PubMed ID: 17159828
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Fetal phenotype of Prader-Willi syndrome due to maternal disomy for chromosome 15.
    L'Herminé AC; Aboura A; Brisset S; Cuisset L; Castaigne V; Labrune P; Frydman R; Tachdjian G
    Prenat Diagn; 2003 Nov; 23(11):938-43. PubMed ID: 14634983
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Complex rearrangements of chromosome 15 in two patients with mild/atypical Prader Willi syndrome.
    Salavoura K; Kolialexi A; Sofocleous C; Kalaitzidaki M; Pampanos A; Kitsiou S; Mavrou A
    Genet Couns; 2008; 19(2):219-24. PubMed ID: 18618997
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
    Gilhuis HJ; van Ravenswaaij CM; Hamel BJ; Gabreëls FJ
    Eur J Paediatr Neurol; 2000; 4(1):39-43. PubMed ID: 10701104
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Differences in behavioural phenotype between parental deletion and maternal uniparental disomy in Prader-Willi syndrome: an ERP study.
    Stauder JE; Boer H; Gerits RH; Tummers A; Whittington J; Curfs LM
    Clin Neurophysiol; 2005 Jun; 116(6):1464-70. PubMed ID: 15978509
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Clinical management of a child with Prader-Willi Syndrome from maternal uniparental disomy (UPD) genetic inheritance.
    Bellon-Harn ML
    J Commun Disord; 2005; 38(6):459-72. PubMed ID: 15979635
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic basis of Prader-Willi syndrome in Korea: less uniparental disomy than has been recognized?
    Kim HJ; Cho HJ; Jin DK; Kwon EK; Ki CS; Kim JW; Kim SH
    Clin Genet; 2004 Oct; 66(4):368-72. PubMed ID: 15355442
    [No Abstract]   [Full Text] [Related]  

  • 12. [Prader-Willi syndrome--clinical picture and genetics].
    Schulze AH; Petersen MB; Blichfeldt SS; Kastrup KW; Brøndum-Nielsen K
    Ugeskr Laeger; 1995 Mar; 157(11):1513-9. PubMed ID: 7725549
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Somatic mosaicism for maternal uniparental disomy 15 in a girl with Prader-Willi syndrome: confirmation by cell cloning and identification of candidate downstream genes.
    Horsthemke B; Nazlican H; Hüsing J; Klein-Hitpass L; Claussen U; Michel S; Lich C; Gillessen-Kaesbach G; Buiting K
    Hum Mol Genet; 2003 Oct; 12(20):2723-32. PubMed ID: 12944418
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes.
    Camprubí C; Coll MD; Villatoro S; Gabau E; Kamli A; Martínez MJ; Poyatos D; Guitart M
    Eur J Med Genet; 2007; 50(1):11-20. PubMed ID: 17095305
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).
    Varela MC; Lopes GM; Koiffmann CP
    Ann Genet; 2004; 47(3):267-73. PubMed ID: 15337472
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Screening of Prader-Willi syndrome and Angelman syndrome in school children with moderate to profound mental retardation in southern Taiwan.
    Su MT; Teng YN; Kuo PL
    Acta Paediatr Taiwan; 2007; 48(2):73-6. PubMed ID: 17626606
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A combination of five short tandem repeats of chromosome 15 significantly improves the identification of Prader-Willi syndrome etiology in the Argentinean population.
    Aráoz HV; Torrado M; Barreiro C; Chertkoff L
    Genet Mol Res; 2006 Jun; 5(2):390-8. PubMed ID: 16819717
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Molecular diagnosis of Prader-Willi and Angelman syndromes: methylation, cytogenetics and FISH analysis].
    Santa María L; Curotto B; Cortés F; Rojas C; Alliende MA
    Rev Med Chil; 2001 Apr; 129(4):367-74. PubMed ID: 11413988
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Molecular markers for diagnosis of Prader-Willi syndrome in thai patients by fish.
    Wiriyaukaradecha S; Patmasiriwat P; Wasant P; Tantiniti P
    Southeast Asian J Trop Med Public Health; 2003 Dec; 34(4):881-6. PubMed ID: 15115105
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
    Klein OD; Cotter PD; Albertson DG; Pinkel D; Tidyman WE; Moore MW; Rauen KA
    Clin Genet; 2004 Jun; 65(6):477-82. PubMed ID: 15151506
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 12.