175 related articles for article (PubMed ID: 1683645)
1. Somatic recombination rather than uniparental disomy suggested as another mechanism by which genetic imprinting may play a role in the etiology of Prader-Willi syndrome.
Gregory CA; Schwartz J; Kirkilionis AJ; Rudd N; Hamerton JL
Hum Genet; 1991 Nov; 88(1):42-8. PubMed ID: 1683645
[TBL] [Abstract][Full Text] [Related]
2. Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.
Gregory CA; Kirkilionis AJ; Greenberg CR; Chudley AE; Hamerton JL
Am J Med Genet; 1990 Apr; 35(4):536-45. PubMed ID: 1970703
[TBL] [Abstract][Full Text] [Related]
3. Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome.
Nicholls RD; Knoll JH; Glatt K; Hersh JH; Brewster TD; Graham JM; Wurster-Hill D; Wharton R; Latt SA
Am J Med Genet; 1989 May; 33(1):66-77. PubMed ID: 2568752
[TBL] [Abstract][Full Text] [Related]
4. Prader-Willi syndrome: diagnostic strategy with a cytogenetic and molecular approach.
Malzac P; Moncla A; Voelckel MA; Livet MO; Girardot L; Mattei MG; Mattei JF
Neuromuscul Disord; 1993; 3(5-6):493-6. PubMed ID: 7910502
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes.
Driscoll DJ; Waters MF; Williams CA; Zori RT; Glenn CC; Avidano KM; Nicholls RD
Genomics; 1992 Aug; 13(4):917-24. PubMed ID: 1505981
[TBL] [Abstract][Full Text] [Related]
7. Molecular and cytogenetic studies of the Prader-Willi syndrome.
Trent RJ; Volpato F; Smith A; Lindeman R; Wong MK; Warne G; Haan E
J Med Genet; 1991 Oct; 28(10):649-54. PubMed ID: 1682493
[TBL] [Abstract][Full Text] [Related]
8. The impact of imprinting: Prader-Willi syndrome resulting from chromosome translocation, recombination, and nondisjunction.
Toth-Fejel S; Olson S; Gunter K; Quan F; Wolford J; Popovich BW; Magenis RE
Am J Hum Genet; 1996 May; 58(5):1008-16. PubMed ID: 8651261
[TBL] [Abstract][Full Text] [Related]
9. Bloom syndrome and maternal uniparental disomy for chromosome 15.
Woodage T; Prasad M; Dixon JW; Selby RE; Romain DR; Columbano-Green LM; Graham D; Rogan PK; Seip JR; Smith A
Am J Hum Genet; 1994 Jul; 55(1):74-80. PubMed ID: 7912890
[TBL] [Abstract][Full Text] [Related]
10. Sporadic occurrence of nondeletion Prader-Willi syndrome in two cases: a female with maternal uniparental disomy and a male with complex chromosomal rearrangement.
Murthy SK; al-Nassar KE; Verghese L
Nutrition; 1995; 11(5 Suppl):650-2. PubMed ID: 8748243
[TBL] [Abstract][Full Text] [Related]
11. Isochromosome 15q of maternal origin in two Prader-Willi syndrome patients previously diagnosed erroneously as cytogenetic deletions.
Saitoh S; Mutirangura A; Kuwano A; Ledbetter DH; Niikawa N
Am J Med Genet; 1994 Mar; 50(1):64-7. PubMed ID: 7909198
[TBL] [Abstract][Full Text] [Related]
12. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome.
Nicholls RD; Knoll JH; Butler MG; Karam S; Lalande M
Nature; 1989 Nov; 342(6247):281-5. PubMed ID: 2812027
[TBL] [Abstract][Full Text] [Related]
13. Origin of uniparental disomy 15 in patients with Prader-Willi or Angelman syndrome.
Fridman C; Koiffmann CP
Am J Med Genet; 2000 Sep; 94(3):249-53. PubMed ID: 10995513
[TBL] [Abstract][Full Text] [Related]
14. Exclusion mapping of the Cohen syndrome gene from the Prader-Willi syndrome locus.
Kondo I; Hamabe J; Yamamoto K; Niikawa N
Clin Genet; 1990 Dec; 38(6):422-6. PubMed ID: 1981180
[TBL] [Abstract][Full Text] [Related]
15. DNA deletion and its parental origin in Angelman syndrome patients.
Hamabe J; Kuroki Y; Imaizumi K; Sugimoto T; Fukushima Y; Yamaguchi A; Izumikawa Y; Niikawa N
Am J Med Genet; 1991 Oct; 41(1):64-8. PubMed ID: 1683160
[TBL] [Abstract][Full Text] [Related]
16. A variety of genetic mechanisms are associated with the Prader-Willi syndrome.
Woodage T; Deng ZM; Prasad M; Smart R; Lindeman R; Christian SL; Ledbetter DH; Robson L; Smith A; Trent RJ
Am J Med Genet; 1994 Sep; 54(3):219-26. PubMed ID: 7810579
[TBL] [Abstract][Full Text] [Related]
17. Routine screening for microdeletions by FISH in 77 patients suspected of having Prader-Willi or Angelman syndromes using YAC clone 273A2 (D15S10).
Erdel M; Schuffenhauer S; Buchholz B; Barth-Witte U; Köchl S; Utermann B; Duba HC; Utermann G
Hum Genet; 1996 Jun; 97(6):784-93. PubMed ID: 8641697
[TBL] [Abstract][Full Text] [Related]
18. A de novo unbalanced reciprocal translocation identified as paternal in origin in the Prader-Willi syndrome.
Smith A; Lindeman R; Volpato F; Kearney A; White S; Haan E; Trent RJ
Hum Genet; 1991 Mar; 86(5):534-6. PubMed ID: 2016095
[TBL] [Abstract][Full Text] [Related]
19. A genetic model for the Prader-Willi syndrome and its implication for Angelman syndrome.
Kennerknecht I
Hum Genet; 1992; 90(1-2):91-8. PubMed ID: 1427794
[TBL] [Abstract][Full Text] [Related]
20. Long-range restriction mapping and linkage analysis of the Prader-Willi chromosome region (PWCR).
Kirkilionis AJ; Gregory CA; Hamerton JL
Genomics; 1991 Mar; 9(3):524-35. PubMed ID: 2032723
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
