607 related articles for article (PubMed ID: 15151506)
1. 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]
2. 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]
3. 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]
4. 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]
5. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.
Calounova G; Novotna D; Simandlova M; Havlovicova M; Zumrová A; Kocarek E; Sedlacek Z
Neuro Endocrinol Lett; 2006 Oct; 27(5):579-85. PubMed ID: 17159828
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. 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]
8. Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome.
Kubota T; Sutcliffe JS; Aradhya S; Gillessen-Kaesbach G; Christian SL; Horsthemke B; Beaudet AL; Ledbetter DH
Am J Med Genet; 1996 Dec; 66(1):77-80. PubMed ID: 8957518
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. 15q duplication associated with autism in a multiplex family with a familial cryptic translocation t(14;15)(q11.2;q13.3) detected using array-CGH.
Koochek M; Harvard C; Hildebrand MJ; Van Allen M; Wingert H; Mickelson E; Holden JJ; Rajcan-Separovic E; Lewis ME
Clin Genet; 2006 Feb; 69(2):124-34. PubMed ID: 16433693
[TBL] [Abstract][Full Text] [Related]
11. A Y/15 translocation in a 45,X male with Prader-Willi syndrome.
Puvabanditsin S; Garrow E; Razi S; Mohar AG; Tadros JJ; Phattraprayoon N; Patel P
Genet Couns; 2007; 18(4):417-21. PubMed ID: 18286823
[TBL] [Abstract][Full Text] [Related]
12. Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients.
Hamabe J; Fukushima Y; Harada N; Abe K; Matsuo N; Nagai T; Yoshioka A; Tonoki H; Tsukino R; Niikawa N
Am J Med Genet; 1991 Oct; 41(1):54-63. PubMed ID: 1683159
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. [Unbalanced translocation t (5;15) in a patient with Prader-Willi syndrome].
Bai JL; Wang H; Yang YL; Song F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):664-7. PubMed ID: 21154328
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A nonimprinted Prader-Willi Syndrome (PWS)-region gene regulates a different chromosomal domain in trans but the imprinted pws loci do not alter genome-wide mRNA levels.
Stefan M; Portis T; Longnecker R; Nicholls RD
Genomics; 2005 May; 85(5):630-40. PubMed ID: 15820315
[TBL] [Abstract][Full Text] [Related]
18. [Prader-Willi syndrome and genomic imprinting].
Wang W; Wang DF; Cui YF; Ni JH; Dong ZY; Fu MF; Fu HM; Lu GQ; Chen FS
Zhonghua Er Ke Za Zhi; 2003 Jun; 41(6):453-6. PubMed ID: 14749005
[TBL] [Abstract][Full Text] [Related]
19. Non-reciprocal translocation (5;15), isodicentric (15) and Prader-Willi syndrome.
Murdock RL; Wurster-Hill DH
Am J Med Genet; 1986 Sep; 25(1):61-9. PubMed ID: 3799724
[TBL] [Abstract][Full Text] [Related]
20. Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome.
Tantravahi U; Nicholls RD; Stroh H; Ringer S; Neve RL; Kaplan L; Wharton R; Wurster-Hill D; Graham JM; Cantú ES
Am J Med Genet; 1989 May; 33(1):78-87. PubMed ID: 2750788
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]