352 related articles for article (PubMed ID: 1427794)
21. 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]
22. 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]
23. Prader-Willi syndrome and Angelman syndrome.
Buiting K
Am J Med Genet C Semin Med Genet; 2010 Aug; 154C(3):365-76. PubMed ID: 20803659
[TBL] [Abstract][Full Text] [Related]
24. Prader-Willi and Angelman syndromes. Disorders of genomic imprinting.
Cassidy SB; Schwartz S
Medicine (Baltimore); 1998 Mar; 77(2):140-51. PubMed ID: 9556704
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. A rapid, PCR based test for differential molecular diagnosis of Prader-Willi and Angelman syndromes.
Chotai KA; Payne SJ
J Med Genet; 1998 Jun; 35(6):472-5. PubMed ID: 9643288
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. Towards a molecular understanding of Prader-Willi and Angelman syndromes.
Mann MR; Bartolomei MS
Hum Mol Genet; 1999; 8(10):1867-73. PubMed ID: 10469839
[TBL] [Abstract][Full Text] [Related]
29. Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11-q13 imprinting region.
Mim RA; Soorajkumar A; Kosaji N; Rahman MM; Sarker S; Karuvantevida N; Eshaque TB; Rahaman MA; Islam A; Chowdhury MSJ; Shams N; Uddin KMF; Akter H; Uddin M
Brain Behav; 2024 Apr; 14(4):e3437. PubMed ID: 38616334
[TBL] [Abstract][Full Text] [Related]
30. Allele specificity of DNA replication timing in the Angelman/Prader-Willi syndrome imprinted chromosomal region.
Knoll JH; Cheng SD; Lalande M
Nat Genet; 1994 Jan; 6(1):41-6. PubMed ID: 8136833
[TBL] [Abstract][Full Text] [Related]
31. Cloning of the breakpoints of a submicroscopic deletion in an Angelman syndrome patient.
Greger V; Woolf E; Lalande M
Hum Mol Genet; 1993 Jul; 2(7):921-4. PubMed ID: 8364575
[TBL] [Abstract][Full Text] [Related]
32. Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations.
Saitoh S; Buiting K; Rogan PK; Buxton JL; Driscoll DJ; Arnemann J; König R; Malcolm S; Horsthemke B; Nicholls RD
Proc Natl Acad Sci U S A; 1996 Jul; 93(15):7811-5. PubMed ID: 8755558
[TBL] [Abstract][Full Text] [Related]
33. Molecular diagnosis of Prader-Willi and Angelman syndromes by methylation-specific melting analysis and methylation-specific multiplex ligation-dependent probe amplification.
Procter M; Chou LS; Tang W; Jama M; Mao R
Clin Chem; 2006 Jul; 52(7):1276-83. PubMed ID: 16690734
[TBL] [Abstract][Full Text] [Related]
34. A transgene insertion creating a heritable chromosome deletion mouse model of Prader-Willi and angelman syndromes.
Gabriel JM; Merchant M; Ohta T; Ji Y; Caldwell RG; Ramsey MJ; Tucker JD; Longnecker R; Nicholls RD
Proc Natl Acad Sci U S A; 1999 Aug; 96(16):9258-63. PubMed ID: 10430930
[TBL] [Abstract][Full Text] [Related]
35. The mechanisms involved in formation of deletions and duplications of 15q11-q13.
Robinson WP; Dutly F; Nicholls RD; Bernasconi F; Peñaherrera M; Michaelis RC; Abeliovich D; Schinzel AA
J Med Genet; 1998 Feb; 35(2):130-6. PubMed ID: 9580159
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. Familial interstitial 570 kbp deletion of the UBE3A gene region causing Angelman syndrome but not Prader-Willi syndrome.
Bürger J; Horn D; Tönnies H; Neitzel H; Reis A
Am J Med Genet; 2002 Aug; 111(3):233-7. PubMed ID: 12210318
[TBL] [Abstract][Full Text] [Related]
38. Genome organization, function, and imprinting in Prader-Willi and Angelman syndromes.
Nicholls RD; Knepper JL
Annu Rev Genomics Hum Genet; 2001; 2():153-75. PubMed ID: 11701647
[TBL] [Abstract][Full Text] [Related]
39. Familial translocation t(Y;15)(q12;p11) and de novo deletion of the Prader-Willi syndrome (PWS) critical region on 15q11-q13.
Eliez S; Morris MA; Dahoun-Hadorn S; DeLozier-Blanchet CD; Gos A; Sizonenko P; Antonarakis SE
Am J Med Genet; 1997 Jun; 70(3):222-8. PubMed ID: 9188657
[TBL] [Abstract][Full Text] [Related]
40. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
Saitoh S; Buiting K; Cassidy SB; Conroy JM; Driscoll DJ; Gabriel JM; Gillessen-Kaesbach G; Glenn CC; Greenswag LR; Horsthemke B; Kondo I; Kuwajima K; Niikawa N; Rogan PK; Schwartz S; Seip J; Williams CA; Nicholls RD
Am J Med Genet; 1997 Jan; 68(2):195-206. PubMed ID: 9028458
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]