289 related articles for article (PubMed ID: 25832033)
1. Phenotype of a child with Angelman syndrome born to a woman with Prader-Willi syndrome.
Ostergaard JR
Am J Med Genet A; 2015 Sep; 167A(9):2138-44. PubMed ID: 25832033
[TBL] [Abstract][Full Text] [Related]
2. Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region.
Jiang YH; Wauki K; Liu Q; Bressler J; Pan Y; Kashork CD; Shaffer LG; Beaudet AL
BMC Genomics; 2008 Jan; 9():50. PubMed ID: 18226259
[TBL] [Abstract][Full Text] [Related]
3. Identification of novel imprinted transcripts in the Prader-Willi syndrome and Angelman syndrome deletion region: further evidence for regional imprinting control.
Lee S; Wevrick R
Am J Hum Genet; 2000 Mar; 66(3):848-58. PubMed ID: 10712201
[TBL] [Abstract][Full Text] [Related]
4. Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes.
Glenn CC; Driscoll DJ; Yang TP; Nicholls RD
Mol Hum Reprod; 1997 Apr; 3(4):321-32. PubMed ID: 9237260
[TBL] [Abstract][Full Text] [Related]
5. Mechanisms of imprinting of the Prader-Willi/Angelman region.
Horsthemke B; Wagstaff J
Am J Med Genet A; 2008 Aug; 146A(16):2041-52. PubMed ID: 18627066
[TBL] [Abstract][Full Text] [Related]
6. Congenital ichthyosis in Prader-Willi syndrome associated with maternal chromosome 15 uniparental disomy: Case report and review of autosomal recessive conditions unmasked by UPD.
Muthusamy K; Macke EL; Klee EW; Tebben PJ; Hand JL; Hasadsri L; Marcou CA; Schimmenti LA
Am J Med Genet A; 2020 Oct; 182(10):2442-2449. PubMed ID: 32815268
[TBL] [Abstract][Full Text] [Related]
7. Fertility in Prader-Willi syndrome: a case report with Angelman syndrome in the offspring.
Schulze A; Mogensen H; Hamborg-Petersen B; Graem N; Ostergaard JR; Brøndum-Nielsen K
Acta Paediatr; 2001 Apr; 90(4):455-9. PubMed ID: 11332942
[TBL] [Abstract][Full Text] [Related]
8. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
Clayton-Smith J; Driscoll DJ; Waters MF; Webb T; Andrews T; Malcolm S; Pembrey ME; Nicholls RD
Am J Med Genet; 1993 Oct; 47(5):683-6. PubMed ID: 8266996
[TBL] [Abstract][Full Text] [Related]
9. Are Angelman and Prader-Willi syndromes more similar than we thought? Food-related behavior problems in Angelman, Cornelia de Lange, fragile X, Prader-Willi and 1p36 deletion syndromes.
Welham A; Lau J; Moss J; Cullen J; Higgs S; Warren G; Wilde L; Marr A; Cook F; Oliver C
Am J Med Genet A; 2015 Mar; 167A(3):572-8. PubMed ID: 25691410
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Modification of 15q11-q13 DNA methylation imprints in unique Angelman and Prader-Willi patients.
Glenn CC; Nicholls RD; Robinson WP; Saitoh S; Niikawa N; Schinzel A; Horsthemke B; Driscoll DJ
Hum Mol Genet; 1993 Sep; 2(9):1377-82. PubMed ID: 8242060
[TBL] [Abstract][Full Text] [Related]
12. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
Kalsner L; Chamberlain SJ
Pediatr Clin North Am; 2015 Jun; 62(3):587-606. PubMed ID: 26022164
[TBL] [Abstract][Full Text] [Related]
13. Familial translocations involving 15q11-q13 can give rise to interstitial deletions causing Prader-Willi or Angelman syndrome.
Horsthemke B; Maat-Kievit A; Sleegers E; van den Ouweland A; Buiting K; Lich C; Mollevanger P; Beverstock G; Gillessen-Kaesbach G; Schwanitz G
J Med Genet; 1996 Oct; 33(10):848-51. PubMed ID: 8933339
[TBL] [Abstract][Full Text] [Related]
14. Does parent of origin matter? Methylation studies should be performed on patients with multiple copies of the Prader-Willi/Angelman syndrome critical region.
Aypar U; Brodersen PR; Lundquist PA; Dawson DB; Thorland EC; Hoppman N
Am J Med Genet A; 2014 Oct; 164A(10):2514-20. PubMed ID: 24975781
[TBL] [Abstract][Full Text] [Related]
15. Combined cytogenetic and molecular analyses for the diagnosis of Prader-Willi/Angelman syndromes.
Borelina D; Engel N; Esperante S; Ferreiro V; Ferrer M; Torrado M; Goldschmidt E; Francipane L; Szijan I
J Biochem Mol Biol; 2004 Sep; 37(5):522-6. PubMed ID: 15479613
[TBL] [Abstract][Full Text] [Related]
16. Molecular characterization of two proximal deletion breakpoint regions in both Prader-Willi and Angelman syndrome patients.
Christian SL; Robinson WP; Huang B; Mutirangura A; Line MR; Nakao M; Surti U; Chakravarti A; Ledbetter DH
Am J Hum Genet; 1995 Jul; 57(1):40-8. PubMed ID: 7611294
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Imprinting center analysis in Prader-Willi and Angelman syndrome patients with typical and atypical phenotypes.
Camprubí C; Coll MD; Villatoro S; Gabau E; Kamli A; Martínez MJ; Poyatos D; Guitart M
Eur J Med Genet; 2007; 50(1):11-20. PubMed ID: 17095305
[TBL] [Abstract][Full Text] [Related]
19. Genomic imprinting and uniparental disomy in Angelman and Prader-Willi syndromes: a review.
Nicholls RD
Am J Med Genet; 1993 Apr; 46(1):16-25. PubMed ID: 8388169
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]