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 *

90 related articles for article (PubMed ID: 9630080)

  • 21. Angelman syndrome in an inbred family.
    Beuten J; Hennekam RC; Van Roy B; Mangelschots K; Sutcliffe JS; Halley DJ; Hennekam FA; Beaudet AL; Willems PJ
    Hum Genet; 1996 Mar; 97(3):294-8. PubMed ID: 8786067
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A case of Angelman syndrome arising as a result of a de novo Robertsonian translocation.
    Ramsden S; Gaunt L; Seres-Santamaria A; Clayton-Smith J
    Acta Genet Med Gemellol (Roma); 1996; 45(1-2):255-61. PubMed ID: 8872042
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Phenotype-genotype correlation in 20 deletion and 20 non-deletion Angelman syndrome patients.
    Moncla A; Malzac P; Voelckel MA; Auquier P; Girardot L; Mattei MG; Philip N; Mattei JF; Lalande M; Livet MO
    Eur J Hum Genet; 1999; 7(2):131-9. PubMed ID: 10196695
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Molecular epigenetics of Angelman syndrome.
    Lalande M; Calciano MA
    Cell Mol Life Sci; 2007 Apr; 64(7-8):947-60. PubMed ID: 17347796
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Angelman syndrome].
    Moncla A; Livet MO; Malzac P; Voelckel MA; Mattei MG; Mattei JF; Giraud F
    Arch Pediatr; 1994 Dec; 1(12):1118-26. PubMed ID: 7849899
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Angelman syndrome with uniparental disomy due to paternal meiosis II nondisjunction.
    Gyftodimou J; Karadima G; Pandelia E; Vassilopoulos D; Petersen MB
    Clin Genet; 1999 Jun; 55(6):483-6. PubMed ID: 10450868
    [TBL] [Abstract][Full Text] [Related]  

  • 27. [Clinical manifestation and EEG characteristics of Angelman syndrome].
    Yang XY; Zou LP; Song F; Zhang LP; Zheng H; Wu HS; Xiao J
    Zhonghua Er Ke Za Zhi; 2010 Oct; 48(10):783-6. PubMed ID: 21176491
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Clinical Application of an Innovative Multiplex-Fluorescent-Labeled STRs Assay for Prader-Willi Syndrome and Angelman Syndrome.
    Zhang K; Liu S; Feng B; Yang Y; Zhang H; Dong R; Liu Y; Gai Z
    PLoS One; 2016; 11(2):e0147824. PubMed ID: 26841067
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Myoclonic status and central fever in Angelman syndrome due to paternal uniparental disomy.
    Nicita F; Garone G; Papetti L; Consoli F; Magliozzi M; De Luca A; Spalice A
    J Neurogenet; 2015; 29(4):178-82. PubMed ID: 26559560
    [TBL] [Abstract][Full Text] [Related]  

  • 30. The spectrum of mutations in UBE3A causing Angelman syndrome.
    Fang P; Lev-Lehman E; Tsai TF; Matsuura T; Benton CS; Sutcliffe JS; Christian SL; Kubota T; Halley DJ; Meijers-Heijboer H; Langlois S; Graham JM; Beuten J; Willems PJ; Ledbetter DH; Beaudet AL
    Hum Mol Genet; 1999 Jan; 8(1):129-35. PubMed ID: 9887341
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Just how happy is the happy puppet? An emotion signaling and kinship theory perspective on the behavioral phenotype of children with Angelman syndrome.
    Brown WM; Consedine NS
    Med Hypotheses; 2004; 63(3):377-85. PubMed ID: 15288352
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Angelman Syndrome due to a Maternally Inherited Intragenic Deletion Encompassing Exons 7 and 8 of the UBE3A Gene.
    Ververi A; Islam L; Bewes B; Busby L; Sullivan C; Canham N
    Cytogenet Genome Res; 2017; 152(3):132-136. PubMed ID: 28898887
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Rapid Diagnosis of Imprinting Disorders Involving Copy Number Variation and Uniparental Disomy Using Genome-Wide SNP Microarrays.
    Liu W; Zhang R; Wei J; Zhang H; Yu G; Li Z; Chen M; Sun X
    Cytogenet Genome Res; 2015; 146(1):9-18. PubMed ID: 26184742
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Angelman syndrome - insights into a rare neurogenetic disorder.
    Buiting K; Williams C; Horsthemke B
    Nat Rev Neurol; 2016 Oct; 12(10):584-93. PubMed ID: 27615419
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Prenatal testing for uniparental disomy: indications and clinical relevance.
    Kotzot D
    Ultrasound Obstet Gynecol; 2008 Jan; 31(1):100-5. PubMed ID: 18059071
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Angelman syndrome: physical characteristics and behavioural phenotype in 37 patients with confirmed genetic diagnosis].
    Galván-Manso M; Campistol J; Monros E; Póo P; Vernet AM; Pineda M; Sans A; Colomer J; Conill JJ; Sanmartí FX
    Rev Neurol; 2002 Sep 1-15; 35(5):425-9. PubMed ID: 12373673
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Neurologic manifestations of Angelman syndrome.
    Thibert RL; Larson AM; Hsieh DT; Raby AR; Thiele EA
    Pediatr Neurol; 2013 Apr; 48(4):271-9. PubMed ID: 23498559
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Genetic imprinting: the paradigm of Prader-Willi and Angelman syndromes.
    Gurrieri F; Accadia M
    Endocr Dev; 2009; 14():20-8. PubMed ID: 19293572
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Increased parental ages and uniparental disomy 15: a paternal age effect?
    Robinson WP; Lorda-Sanchez I; Malcolm S; Langlois S; Schuffenhauer S; Knoblauch H; Horsthemke B; Schinzel AA
    Eur J Hum Genet; 1993; 1(4):280-6. PubMed ID: 8081941
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 5.