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 *

79 related articles for article (PubMed ID: 9128934)

  • 1. Inherited unbalanced subtelomeric translocation in a child with 8p- and Angelman syndromes.
    Wenger SL; Sell SL; Painter MJ; Steele MW
    Am J Med Genet; 1997 May; 70(2):150-4. PubMed ID: 9128934
    [TBL] [Abstract][Full Text] [Related]  

  • 2. True telomeric translocation in a baby with the Prader-Willi phenotype.
    Reeve A; Norman A; Sinclair P; Whittington-Smith R; Hamey Y; Donnai D; Read A
    Am J Med Genet; 1993 Aug; 47(1):1-6. PubMed ID: 8368237
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Recurrent rearrangements in the proximal 15q11-q14 region: a new breakpoint cluster specific to unbalanced translocations.
    Mignon-Ravix C; Depetris D; Luciani JJ; Cuoco C; Krajewska-Walasek M; Missirian C; Collignon P; Delobel B; Croquette MF; Moncla A; Kroisel PM; Mattei MG
    Eur J Hum Genet; 2007 Apr; 15(4):432-40. PubMed ID: 17264869
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Familial complex chromosome rearrangement giving rise to balanced and unbalanced recombination products.
    Zahed L; Der Kaloustian V; Batanian JR
    Am J Med Genet; 1998 Aug; 79(1):30-4. PubMed ID: 9738865
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Difficulties of genetic counseling and prenatal diagnosis in a consanguineous couple segregating for the same translocation (14;15) (q11;q13) and at risk for Prader-Willi and Angelman syndromes.
    Flori E; Biancalana V; Girard-Lemaire F; Favre R; Flori J; Doray B; Mandel JL
    Eur J Hum Genet; 2004 Mar; 12(3):181-6. PubMed ID: 14694357
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [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]  

  • 8. Investigations with fluorescence in situ hybridization (FISH) demonstrate loss of the telomeres on the reciprocal chromosome in three unbalanced translocations involving chromosome 15 in the Prader-Willi and Angelman syndromes.
    Jauch A; Robson L; Smith A
    Hum Genet; 1995 Sep; 96(3):345-9. PubMed ID: 7649555
    [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. Detection of a novel familial deletion of four genes between BP1 and BP2 of the Prader-Willi/Angelman syndrome critical region by oligo-array CGH in a child with neurological disorder and speech impairment.
    Murthy SK; Nygren AO; El Shakankiry HM; Schouten JP; Al Khayat AI; Ridha A; Al Ali MT
    Cytogenet Genome Res; 2007; 116(1-2):135-40. PubMed ID: 17268193
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Identification of a subtle t(16;19)(p13.3;p13.3) in an infant with multiple congenital abnormalities using a 12-colour multiplex FISH telomere assay, M-TEL.
    Brown J; Horsley SW; Jung C; Saracoglu K; Janssen B; Brough M; Daschner M; Beedgen B; Kerkhoffs G; Eils R; Harris PC; Jauch A; Kearney L
    Eur J Hum Genet; 2000 Dec; 8(12):903-10. PubMed ID: 11175277
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
    Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
    J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Maternal disomy and Prader-Willi syndrome consistent with gamete complementation in a case of familial translocation (3;15) (p25;q11.2).
    Park JP; Moeschler JB; Hani VH; Hawk AB; Belloni DR; Noll WW; Mohandas TK
    Am J Med Genet; 1998 Jun; 78(2):134-9. PubMed ID: 9674903
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Paternal uniparental disomy in a child with a balanced 15;15 translocation and Angelman syndrome.
    Freeman SB; May KM; Pettay D; Fernhoff PM; Hassold TJ
    Am J Med Genet; 1993 Mar; 45(5):625-30. PubMed ID: 8456836
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Electroclinical characteristics of seizures-comparing Prader--Willi syndrome with Angelman syndrome.
    Wang PJ; Hou JW; Sue WC; Lee WT
    Brain Dev; 2005 Mar; 27(2):101-7. PubMed ID: 15668048
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Unbalanced translocation der(11)t(11;12)(q23;q13): a new recurrent cytogenetic aberration in myelodysplastic syndrome with a complex karyotype.
    Yamamoto K; Hato A; Minagawa K; Yakushijin K; Urahama N; Gomyo H; Sada A; Okamura A; Ito M; Matsui T
    Cancer Genet Cytogenet; 2004 Nov; 155(1):67-73. PubMed ID: 15527905
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 4.