264 related articles for article (PubMed ID: 9152837)
1. Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.
Devriendt K; Petit P; Matthijs G; Vermeesch JR; Holvoet M; De Muelenaere A; Marynen P; Cassiman JJ; Fryns JP
J Med Genet; 1997 May; 34(5):395-9. PubMed ID: 9152837
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. 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]
5. Nonreciprocal and jumping translocations of 15q1----qter in Prader-Willi syndrome.
Rivera H; Zuffardi O; Gargantini L
Am J Med Genet; 1990 Nov; 37(3):311-7. PubMed ID: 2260556
[TBL] [Abstract][Full Text] [Related]
6. Mosaicism of proximal 15q duplication/deletion resulting in Prader-Willi syndrome with normal methylation.
Boyd L; Brown MG; Kelson S; Lawce H; Shuttleworth S; Unsworth N; Magenis RE
Am J Med Genet A; 2005 Oct; 138A(2):181-4. PubMed ID: 16100727
[No Abstract] [Full Text] [Related]
7. 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]
8. Balanced translocation 46,XY,t(2;15)(q37.2;q11.2) associated with atypical Prader-Willi syndrome.
Conroy JM; Grebe TA; Becker LA; Tsuchiya K; Nicholls RD; Buiting K; Horsthemke B; Cassidy SB; Schwartz S
Am J Hum Genet; 1997 Aug; 61(2):388-94. PubMed ID: 9311744
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. A case of an atypically large proximal 15q deletion as cause for Prader-Willi syndrome arising from a de novo unbalanced translocation.
Hickey SE; Thrush DL; Walters-Sen L; Reshmi SC; Astbury C; Gastier-Foster JM; Atkin J
Eur J Med Genet; 2013 Sep; 56(9):510-4. PubMed ID: 23856564
[TBL] [Abstract][Full Text] [Related]
11. Prader-Willi syndrome in a child with mosaic trisomy 15 and mosaic triplo-X: a molecular analysis.
Devriendt K; Matthijs G; Claes S; Legius E; Proesmans W; Cassiman JJ; Fryns JP
J Med Genet; 1997 Apr; 34(4):318-22. PubMed ID: 9138157
[TBL] [Abstract][Full Text] [Related]
12. Interstitial telomeric sequences at the junction site of a jumping translocation.
Vermeesch JR; Petit P; Speleman F; Devriendt K; Fryns JP; Marynen P
Hum Genet; 1997 Jun; 99(6):735-7. PubMed ID: 9187665
[TBL] [Abstract][Full Text] [Related]
13. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.
Burrage LC; Person RE; Flores A; Villanos MT; Bi W; Wiszniewska J; Bacino CA
Am J Med Genet A; 2012 Oct; 158A(10):2557-63. PubMed ID: 22903639
[TBL] [Abstract][Full Text] [Related]
14. Trisomy 9p and Prader-Willi syndromes in an infant resulting from a de-novo unbalanced t(9;15) translocation.
Carter MT; Jacob FD; Sinclair-Bourque E; Ray R; Allanson JE
Clin Dysmorphol; 2009 Apr; 18(2):103-106. PubMed ID: 19282755
[TBL] [Abstract][Full Text] [Related]
15. Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndrome.
Schüle B; Albalwi M; Northrop E; Francis DI; Rowell M; Slater HR; Gardner RJ; Francke U
BMC Med Genet; 2005 May; 6():18. PubMed ID: 15877813
[TBL] [Abstract][Full Text] [Related]
16. Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint.
Schulze A; Hansen C; Skakkebaek NE; Brøndum-Nielsen K; Ledbeter DH; Tommerup N
Nat Genet; 1996 Apr; 12(4):452-4. PubMed ID: 8630505
[TBL] [Abstract][Full Text] [Related]
17. Molecular characterization of a unique de novo 15q deletion associated with Prader-Willi syndrome and central visual impairment.
Windpassinger C; Petek E; Wagner K; Langmann A; Buiting K; Kroisel PM
Clin Genet; 2003 Apr; 63(4):297-302. PubMed ID: 12702163
[TBL] [Abstract][Full Text] [Related]
18. Segmental maternal heterodisomy of the proximal part of chromosome 15 in an infant with Prader-Willi syndrome.
Nazarenko S; Sazhenova E; Baumer A; Schinzel A
Eur J Hum Genet; 2004 May; 12(5):411-4. PubMed ID: 14997184
[TBL] [Abstract][Full Text] [Related]
19. A patient with Prader-Willi syndrome and a supernumerary marker chromosome r(15)(q11.1-13p11.1)pat and maternal heterodisomy.
Werner M; Ben-Neriah Z; Silverstein S; Lerer I; Dagan Y; Abeliovich D
Am J Med Genet A; 2004 Aug; 129A(2):176-9. PubMed ID: 15316980
[TBL] [Abstract][Full Text] [Related]
20. Cytogenetic and age-dependent risk factors associated with uniparental disomy 15.
Robinson WP; Langlois S; Schuffenhauer S; Horsthemke B; Michaelis RC; Christian S; Ledbetter DH; Schinzel A
Prenat Diagn; 1996 Sep; 16(9):837-44. PubMed ID: 8905898
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]