187 related articles for article (PubMed ID: 8644742)
21. Detection of aberrant DNA methylation in unique Prader-Willi syndrome patients and its diagnostic implications.
Buiting K; Dittrich B; Robinson WP; Guitart M; Abeliovich D; Lerer I; Horsthemke B
Hum Mol Genet; 1994 Jun; 3(6):893-5. PubMed ID: 7951232
[TBL] [Abstract][Full Text] [Related]
22. Allele-specific replication of 15q11-q13 loci: a diagnostic test for detection of uniparental disomy.
White LM; Rogan PK; Nicholls RD; Wu BL; Korf B; Knoll JH
Am J Hum Genet; 1996 Aug; 59(2):423-30. PubMed ID: 8755930
[TBL] [Abstract][Full Text] [Related]
23. The chromosome 15 imprinting centre (IC) region has undergone multiple duplication events and contains an upstream exon of SNRPN that is deleted in all Angelman syndrome patients with an IC microdeletion.
Färber C; Dittrich B; Buiting K; Horsthemke B
Hum Mol Genet; 1999 Feb; 8(2):337-43. PubMed ID: 9931342
[TBL] [Abstract][Full Text] [Related]
24. Deletions of a differentially methylated CpG island at the SNRPN gene define a putative imprinting control region.
Sutcliffe JS; Nakao M; Christian S; Orstavik KH; Tommerup N; Ledbetter DH; Beaudet AL
Nat Genet; 1994 Sep; 8(1):52-8. PubMed ID: 7987392
[TBL] [Abstract][Full Text] [Related]
25. FISH ordering of reference markers and of the gene for the alpha 5 subunit of the gamma-aminobutyric acid receptor (GABRA5) within the Angelman and Prader-Willi syndrome chromosomal regions.
Knoll JH; Sinnett D; Wagstaff J; Glatt K; Wilcox AS; Whiting PM; Wingrove P; Sikela JM; Lalande M
Hum Mol Genet; 1993 Feb; 2(2):183-9. PubMed ID: 8388764
[TBL] [Abstract][Full Text] [Related]
26. A case of Prader-Willi syndrome arising as a result of familial unbalanced translocation t(11;15)(q25;q13).
Krajewska Walasek M; Gutkowska A; Bielińska B; Goryluk-Kozakiewicz B; Popowska E
Clin Genet; 1998 Jul; 54(1):60-4. PubMed ID: 9727742
[TBL] [Abstract][Full Text] [Related]
27. Mouse imprinting defect mutations that model Angelman syndrome.
Wu MY; Chen KS; Bressler J; Hou A; Tsai TF; Beaudet AL
Genesis; 2006 Jan; 44(1):12-22. PubMed ID: 16397868
[TBL] [Abstract][Full Text] [Related]
28. FISH detection of chromosome 15 deletions in Prader-Willi and Angelman syndromes.
Teshima I; Chadwick D; Chitayat D; Kobayashi J; Ray P; Shuman C; Siegel-Bartelt J; Strasberg P; Weksberg R
Am J Med Genet; 1996 Mar; 62(3):217-23. PubMed ID: 8882776
[TBL] [Abstract][Full Text] [Related]
29. [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]
30. Methylation analysis at three different loci within the imprinted region of chromosome 15q11-13.
Buchholz T; Jackson J; Smith A
Am J Med Genet; 1997 Oct; 72(1):117-9. PubMed ID: 9295088
[No Abstract] [Full Text] [Related]
31. Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene.
Dittrich B; Buiting K; Korn B; Rickard S; Buxton J; Saitoh S; Nicholls RD; Poustka A; Winterpacht A; Zabel B; Horsthemke B
Nat Genet; 1996 Oct; 14(2):163-70. PubMed ID: 8841186
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Imprinting analysis of three genes in the Prader-Willi/Angelman region: SNRPN, E6-associated protein, and PAR-2 (D15S225E).
Nakao M; Sutcliffe JS; Durtschi B; Mutirangura A; Ledbetter DH; Beaudet AL
Hum Mol Genet; 1994 Feb; 3(2):309-15. PubMed ID: 8004100
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Angelman syndrome associated with a maternal 15q11-13 deletion of less than 200 kb.
Buxton JL; Chan CT; Gilbert H; Clayton-Smith J; Burn J; Pembrey M; Malcolm S
Hum Mol Genet; 1994 Aug; 3(8):1409-13. PubMed ID: 7987324
[TBL] [Abstract][Full Text] [Related]
36. Breakage in the SNRPN locus in a balanced 46,XY,t(15;19) Prader-Willi syndrome patient.
Sun Y; Nicholls RD; Butler MG; Saitoh S; Hainline BE; Palmer CG
Hum Mol Genet; 1996 Apr; 5(4):517-24. PubMed ID: 8845846
[TBL] [Abstract][Full Text] [Related]
37. Counselling dilemmas associated with the molecular characterisation of two Angelman syndrome families.
Gilbert HL; Buxton JL; Chan CT; McKay T; Cottrell S; Ramsden S; Winter RM; Pembrey ME; Malcolm S
J Med Genet; 1997 Aug; 34(8):651-5. PubMed ID: 9279757
[TBL] [Abstract][Full Text] [Related]
38. The SNRPN promoter is not required for genomic imprinting of the Prader-Willi/Angelman domain in mice.
Bressler J; Tsai TF; Wu MY; Tsai SF; Ramirez MA; Armstrong D; Beaudet AL
Nat Genet; 2001 Jul; 28(3):232-40. PubMed ID: 11431693
[TBL] [Abstract][Full Text] [Related]
39. DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting.
Glenn CC; Deng G; Michaelis RC; Tarleton J; Phelan MC; Surh L; Yang TP; Driscoll DJ
Prenat Diagn; 2000 Apr; 20(4):300-6. PubMed ID: 10740202
[TBL] [Abstract][Full Text] [Related]
40. A targeted deletion upstream of Snrpn does not result in an imprinting defect.
Peery EG; Elmore MD; Resnick JL; Brannan CI; Johnstone KA
Mamm Genome; 2007 Apr; 18(4):255-62. PubMed ID: 17514346
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
