135 related articles for article (PubMed ID: 3799724)
1. 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]
2. The cytogenetic controversy in the Prader-Labhart-Willi syndrome.
Kousseff BG
Am J Med Genet; 1982 Dec; 13(4):431-9. PubMed ID: 7158643
[TBL] [Abstract][Full Text] [Related]
3. 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]
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. Unique karyotypes in two patients with Prader-Willi syndrome.
Narahara K; Hiramoto K; Murakami M; Miyake S; Tsuji K; Yokoyama Y; Namba H; Ninomiya S; Murakami R; Seino Y
Am J Med Genet; 1992 Mar; 42(5):671-7. PubMed ID: 1632436
[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. Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndrome.
Qumsiyeh MB; Dalton JD; Gordon PL; Wilroy RS; Tharapel AT
Am J Med Genet; 1992 Jan; 42(1):109-11. PubMed ID: 1308348
[TBL] [Abstract][Full Text] [Related]
9. Deletions of proximal 15q without Prader-Willi syndrome.
Greenberg F; Ledbetter DH
Am J Med Genet; 1987 Dec; 28(4):813-20. PubMed ID: 3688019
[TBL] [Abstract][Full Text] [Related]
10. Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes.
Schwartz S; Max SR; Panny SR; Cohen MM
Am J Med Genet; 1985 Feb; 20(2):255-63. PubMed ID: 2858158
[TBL] [Abstract][Full Text] [Related]
11. [Chromosome aberrations in Prader-Willi-Labhart syndrome--critical review, documented by 4 unusual cases].
Pfeiffer RA; Tschech L; Irle U; Wündisch GF
Klin Padiatr; 1987; 199(5):329-35. PubMed ID: 3316824
[TBL] [Abstract][Full Text] [Related]
12. Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
Gilhuis HJ; van Ravenswaaij CM; Hamel BJ; Gabreëls FJ
Eur J Paediatr Neurol; 2000; 4(1):39-43. PubMed ID: 10701104
[TBL] [Abstract][Full Text] [Related]
13. Duplication of proximal 15q as a cause of Prader-Willi syndrome.
Pettigrew AL; Gollin SM; Greenberg F; Riccardi VM; Ledbetter DH
Am J Med Genet; 1987 Dec; 28(4):791-802. PubMed ID: 3688017
[TBL] [Abstract][Full Text] [Related]
14. De novo (15;21) unbalanced translocation of paternal origin in a girl with Prader-Willi syndrome.
Cuoco C; Bicocchi MP; Granata D; Mezzano P; Serra G
Am J Med Genet; 1990 Sep; 37(1):62-4. PubMed ID: 2240045
[TBL] [Abstract][Full Text] [Related]
15. Classical Prader-Willi syndrome with trisomy 15(pter----q12) plus de novo variant 15p11.
Smith A; Den Dulk G; Lipson A; Suter M
Ann Genet; 1989; 32(1):39-42. PubMed ID: 2751247
[TBL] [Abstract][Full Text] [Related]
16. Proximal trisomy 13q and distal monosomy 8p in a dysmorphic and mentally retarded patient with an isodicentric chromosome 13q and a 13q/8p translocation chromosome.
Lukusa T; van den Berghe L; Smeets E; Fryns JP
Ann Genet; 1999; 42(4):215-20. PubMed ID: 10674161
[TBL] [Abstract][Full Text] [Related]
17. Neonatal diagnosis of Prader-Willi syndrome and its implications.
Greenberg F; Elder FF; Ledbetter DH
Am J Med Genet; 1987 Dec; 28(4):845-56. PubMed ID: 3688023
[TBL] [Abstract][Full Text] [Related]
18. Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?
Kousseff BG; Diamond T; Essig Y; Miller K; Tedesco T
Am J Med Genet; 1987 Dec; 28(4):803-11. PubMed ID: 3688018
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. t(15;21)(q15;q22.1) pat resulting in partial trisomy and partial monosomy of chromosomes 15 and 21 in two offspring.
Abeliovich D; Dagan J; Lerer I; Silberstein S; Katznelson MB; Frydman M
Am J Med Genet; 1996 Dec; 66(1):45-51. PubMed ID: 8957510
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
