84 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]