405 related articles for article (PubMed ID: 15479613)
41. [Quick diagnosis of Prader-Willi and Angelman syndromes by means of methylation test by PCR].
Huerta Rivas C; Barabash Bustelo A; Gallego Merlo J; Ramos Corrales C; Osorio Cabrero A; Robledo Batanero M; Benítez Ortiz J
An Esp Pediatr; 1998 Jun; 48(6):583-6. PubMed ID: 9662840
[TBL] [Abstract][Full Text] [Related]
42. A modified MS-PCR approach to diagnose patients with Prader-Willi and Angelman syndrome.
Dos Santos JF; Mota LR; Rocha PH; Ferreira de Lima RL
Mol Biol Rep; 2016 Nov; 43(11):1221-1225. PubMed ID: 27535666
[TBL] [Abstract][Full Text] [Related]
43. Prader-Willi syndrome: clinical genetics, cytogenetics and molecular biology.
Bittel DC; Butler MG
Expert Rev Mol Med; 2005 Jul; 7(14):1-20. PubMed ID: 16038620
[TBL] [Abstract][Full Text] [Related]
44. Mosaicism for maternal uniparental disomy 15 in a boy with some clinical features of Prader-Willi syndrome.
Zilina O; Kahre T; Talvik I; Oiglane-Shlik E; Tillmann V; Ounap K
Eur J Med Genet; 2014; 57(6):279-83. PubMed ID: 24704109
[TBL] [Abstract][Full Text] [Related]
45. [Molecular genetic study of causes of the Prader-Willi and Angelman syndrome].
Capková CP; Vrtĕl R; Santavá A; Zapletalová J; Krsiaková J; Hyjánek J; Santavý J
Cas Lek Cesk; 2005; 144(2):113-8. PubMed ID: 15807298
[TBL] [Abstract][Full Text] [Related]
46. Validation studies of SNRPN methylation as a diagnostic test for Prader-Willi syndrome.
Kubota T; Sutcliffe JS; Aradhya S; Gillessen-Kaesbach G; Christian SL; Horsthemke B; Beaudet AL; Ledbetter DH
Am J Med Genet; 1996 Dec; 66(1):77-80. PubMed ID: 8957518
[TBL] [Abstract][Full Text] [Related]
47. 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]
48. Referral diagnosis of Prader-Willi syndrome and Angelman syndrome based on methylation-specific polymerase chain reaction.
Teng YN; Tsai WH; Wu CJ; Lin SJ; Chen YJ; Kuo PL
J Formos Med Assoc; 2002 Jul; 101(7):488-94. PubMed ID: 12353341
[TBL] [Abstract][Full Text] [Related]
49. [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]
50. Molecular genetic diagnostics of Prader-Willi Syndrome: a validation of linkage analysis for the Chinese population.
Li H; Meng S; Chen Z; Li H; Du M; Ma H; Wei H; Duan H; Zheng H; Wenren Q; Song X
J Genet Genomics; 2007 Oct; 34(10):885-91. PubMed ID: 17945167
[TBL] [Abstract][Full Text] [Related]
51. Prevalence of Angelman syndrome and Prader-Willi syndrome in Estonian children: sister syndromes not equally represented.
Oiglane-Shlik E; Talvik T; Zordania R; Põder H; Kahre T; Raukas E; Ilus T; Tasa G; Bartsch O; Väisänen ML; Ounap K
Am J Med Genet A; 2006 Sep; 140(18):1936-43. PubMed ID: 16906556
[TBL] [Abstract][Full Text] [Related]
52. 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]
53. Maternal uniparental disomy in a patient with Prader-Willi syndrome with an additional small inv dup(15) chromosome.
Wang YM; Chuang L; Wang BT; Kuo PL
J Formos Med Assoc; 2004 Dec; 103(12):943-7. PubMed ID: 15624046
[TBL] [Abstract][Full Text] [Related]
54. 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]
55. 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]
56. Methylation-specific multiplex ligation-dependent probe amplification analysis of subjects with chromosome 15 abnormalities.
Bittel DC; Kibiryeva N; Butler MG
Genet Test; 2007; 11(4):467-75. PubMed ID: 18294067
[TBL] [Abstract][Full Text] [Related]
57. Angelman syndrome and prenatally diagnosed Prader-Willi syndrome in first cousins.
Ranganath P; Agarwal M; Phadke SR
Am J Med Genet A; 2011 Nov; 155A(11):2788-90. PubMed ID: 21964995
[TBL] [Abstract][Full Text] [Related]
58. De novo interstitial duplication of 15q11.2-q13.1 with complex maternal uniparental trisomy for the 15q11-q13 region in a patient with Prader-Willi syndrome.
Burrage LC; Person RE; Flores A; Villanos MT; Bi W; Wiszniewska J; Bacino CA
Am J Med Genet A; 2012 Oct; 158A(10):2557-63. PubMed ID: 22903639
[TBL] [Abstract][Full Text] [Related]
59. Clinical-neurologic, cytogenetic and molecular aspects of the Prader-Willi and Angelman syndromes.
de Pina-Neto JM; Ferraz VE; de Molfetta GA; Buxton J; Richards S; Malcolm S
Arq Neuropsiquiatr; 1997 Jun; 55(2):199-208. PubMed ID: 9629378
[TBL] [Abstract][Full Text] [Related]
60. Molecular, cytogenetic, and clinical investigations of Prader-Willi syndrome patients.
Robinson WP; Bottani A; Xie YG; Balakrishman J; Binkert F; Mächler M; Prader A; Schinzel A
Am J Hum Genet; 1991 Dec; 49(6):1219-34. PubMed ID: 1684085
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
