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 *

99 related articles for article (PubMed ID: 10563486)

  • 1. Interstitial 4p deletion in a child with an Angelman syndrome-like phenotype.
    Innes AM; Chudley AE; Carson NL; Dawson AJ
    Clin Genet; 1999 Sep; 56(3):238-41. PubMed ID: 10563486
    [No Abstract]   [Full Text] [Related]  

  • 2. A de novo 15q13.2q13.3 deletion in a boy with an Angelman syndrome like phenotype.
    Barøy T; Misceo D; Braaten O; Helle JR; Fannemel M; Strømme P; Frengen E
    Eur J Med Genet; 2010; 53(4):221-4. PubMed ID: 20382277
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Angelman syndrome in three siblings: genetic model of epilepsy associated with chromosomal DNA deletion of the GABAA receptor.
    Sugimoto T; Araki A; Yasuhara A; Woo M; Nishida N; Sasaki T
    Jpn J Psychiatry Neurol; 1994 Jun; 48(2):271-3. PubMed ID: 7807743
    [No Abstract]   [Full Text] [Related]  

  • 4. Angelman syndrome with a chromosomal inversion 15 inv(p11q13) accompanied by a deletion in 15q11q13.
    Webb T; Clayton-Smith J; Cheng XJ; Knoll JH; Lalande M; Pembrey ME; Malcolm S
    J Med Genet; 1992 Dec; 29(12):921-4. PubMed ID: 1362225
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exclusion of the GABAA-receptor beta 3 subunit gene as the Angelman's syndrome gene.
    Reis A; Kunze J; Ladanyi L; Enders H; Klein-Vogler U; Niemann G
    Lancet; 1993 Jan; 341(8837):122-3. PubMed ID: 8093396
    [No Abstract]   [Full Text] [Related]  

  • 6. Angelman syndrome caused by an identical familial 1,487-kb deletion.
    Sato K; Iwakoshi M; Shimokawa O; Sakai H; Ohta T; Saitoh S; Miyake N; Niikawa N; Harada N; Saitsu H; Mizuguchi T; Matsumoto N
    Am J Med Genet A; 2007 Jan; 143A(1):98-101. PubMed ID: 17152063
    [No Abstract]   [Full Text] [Related]  

  • 7. Deletion of 15q12 in Angelman syndrome: report of 3 new cases.
    Tonk V; Wyandt HE; Michand L; Milunsky A
    Clin Genet; 1992 Nov; 42(5):229-33. PubMed ID: 1486699
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.
    Robinson WP; Wagstaff J; Bernasconi F; Baccichetti C; Artifoni L; Franzoni E; Suslak L; Shih LY; Aviv H; Schinzel AA
    J Med Genet; 1993 Sep; 30(9):756-60. PubMed ID: 8411071
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Deletion involving D15S113 in a mother and son without Angelman syndrome: refinement of the Angelman syndrome critical deletion region.
    Michaelis RC; Skinner SA; Lethco BA; Simensen RJ; Donlon TA; Tarleton J; Phelan MC
    Am J Med Genet; 1995 Jan; 55(1):120-6. PubMed ID: 7702085
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Toxic hepatitis in a case of Angelman syndrome associated with Lennox-Gastaut syndrome.
    Deda G; Caksen H; Kansu A; Girgin N; Suskan E; Uysal S; Tükün A
    Genet Couns; 2004; 15(3):357-61. PubMed ID: 15517829
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Angelman syndrome caused by loss of a marker chromosome: cytogenetic and fluorescence in situ hybridization analysis.
    Arrieta I; Criado B; Nuñez T; Telez M; Echarri A; Martinez B; Castedo S
    Psychiatr Genet; 1997; 7(4):153-8. PubMed ID: 9460799
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Are specific short arm variants or heteromorphisms over-represented in the chromosome 15 deletion in Angelman or Prader-Willi syndrome patients?
    Butler MG
    Am J Med Genet; 1994 Mar; 50(1):42-5. PubMed ID: 8160752
    [No Abstract]   [Full Text] [Related]  

  • 13. Periventricular heterotopia in a boy with interstitial deletion of chromosome 4p.
    Gawlik-Kuklinska K; Wierzba J; Wozniak A; Iliszko M; Debiec-Rychter M; Dubaniewicz-Wybieralska M; Limon J
    Eur J Med Genet; 2008; 51(2):165-71. PubMed ID: 18243084
    [TBL] [Abstract][Full Text] [Related]  

  • 14. The human genome: detecting chromosomal deletions: Angelman and Prader-Willi syndromes.
    Morris-Rosendahl DJ; Back E
    Am J Psychiatry; 2002 Mar; 159(3):372. PubMed ID: 11869997
    [No Abstract]   [Full Text] [Related]  

  • 15. Robertsonian (15q;15q) translocation in a child with Angelman syndrome: evidence of uniparental disomy.
    Tonk V; Schultz RA; Christian SL; Kubota T; Ledbetter DH; Wilson GN
    Am J Med Genet; 1996 Dec; 66(4):426-8. PubMed ID: 8989460
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Environmental influences on the behavioral phenotype of Angelman syndrome.
    Horsler K; Oliver C
    Am J Ment Retard; 2006 Sep; 111(5):311-21. PubMed ID: 16968140
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Mild phenotype in interstitial 4p deletion: another patient and review of the literature.
    Van de Graaf G; Sijstermans JM; Engelen JJ; Schrander-Stumpel CT
    Genet Couns; 1997; 8(1):13-8. PubMed ID: 9101273
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Supernumerary inv dup(15) in a patient with Angelman syndrome and a deletion of 15q11-q13.
    Spinner NB; Zackai E; Cheng SD; Knoll JH
    Am J Med Genet; 1995 May; 57(1):61-5. PubMed ID: 7645601
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10).
    Erdel M; Schuffenhauer S; Buchholz B; Barth-Witte U; Köchl S; Utermann B; Duba HC; Utermann G
    Hum Genet; 1996 Jun; 97(6):784-93. PubMed ID: 8641697
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Apparent germline mosaicism for a 15q11-q13 deletion causing recurrent Angelman syndrome in a Chinese family.
    Tang HS; Wang DG; Xie XM; Li DZ
    Eur J Obstet Gynecol Reprod Biol; 2019 May; 236():255-257. PubMed ID: 30890277
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 5.