459 related articles for article (PubMed ID: 2812027)
1. 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]
2. Chromosome 15 uniparental disomy is not frequent in Angelman syndrome.
Knoll JH; Glatt KA; Nicholls RD; Malcolm S; Lalande M
Am J Hum Genet; 1991 Jan; 48(1):16-21. PubMed ID: 1985457
[TBL] [Abstract][Full Text] [Related]
3. The frequency of uniparental disomy in Prader-Willi syndrome. Implications for molecular diagnosis.
Mascari MJ; Gottlieb W; Rogan PK; Butler MG; Waller DA; Armour JA; Jeffreys AJ; Ladda RL; Nicholls RD
N Engl J Med; 1992 Jun; 326(24):1599-607. PubMed ID: 1584261
[TBL] [Abstract][Full Text] [Related]
4. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion.
Knoll JH; Nicholls RD; Magenis RE; Graham JM; Lalande M; Latt SA
Am J Med Genet; 1989 Feb; 32(2):285-90. PubMed ID: 2564739
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Multiplex PCR of three dinucleotide repeats in the Prader-Willi/Angelman critical region (15q11-q13): molecular diagnosis and mechanism of uniparental disomy.
Mutirangura A; Greenberg F; Butler MG; Malcolm S; Nicholls RD; Chakravarti A; Ledbetter DH
Hum Mol Genet; 1993 Feb; 2(2):143-51. PubMed ID: 8499903
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Familial Prader-Willi syndrome: case report and a literature review.
McEntagart ME; Webb T; Hardy C; King MD
Clin Genet; 2000 Sep; 58(3):216-23. PubMed ID: 11076044
[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. A molecular and cytogenetic study in Finnish Prader-Willi patients.
Kokkonen H; Kähkönen M; Leisti J
Hum Genet; 1995 May; 95(5):568-71. PubMed ID: 7759080
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Exclusion of SNRPN as a major determinant of Prader-Willi syndrome by a translocation breakpoint.
Schulze A; Hansen C; Skakkebaek NE; Brøndum-Nielsen K; Ledbeter DH; Tommerup N
Nat Genet; 1996 Apr; 12(4):452-4. PubMed ID: 8630505
[TBL] [Abstract][Full Text] [Related]
14. Family studies in Prader-Willi syndrome.
Webb T; Hardy CA; Dahlitz M; Watkiss E; Clarke D
Genet Couns; 1994; 5(4):329-36. PubMed ID: 7888134
[TBL] [Abstract][Full Text] [Related]
15. Localization of the gene encoding the GABAA receptor beta 3 subunit to the Angelman/Prader-Willi region of human chromosome 15.
Wagstaff J; Knoll JH; Fleming J; Kirkness EF; Martin-Gallardo A; Greenberg F; Graham JM; Menninger J; Ward D; Venter JC
Am J Hum Genet; 1991 Aug; 49(2):330-7. PubMed ID: 1714232
[TBL] [Abstract][Full Text] [Related]
16. Prader-Willi syndrome due to uniparental disomy in a patient with a balanced chromosomal translocation.
Calounova G; Novotna D; Simandlova M; Havlovicova M; Zumrová A; Kocarek E; Sedlacek Z
Neuro Endocrinol Lett; 2006 Oct; 27(5):579-85. PubMed ID: 17159828
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Salivary abnormalities in Prader-Willi syndrome.
Hart PS
Ann N Y Acad Sci; 1998 Apr; 842():125-31. PubMed ID: 9599302
[TBL] [Abstract][Full Text] [Related]
19. Maternal but not paternal transmission of 15q11-13-linked nondeletion Angelman syndrome leads to phenotypic expression.
Wagstaff J; Knoll JH; Glatt KA; Shugart YY; Sommer A; Lalande M
Nat Genet; 1992 Jul; 1(4):291-4. PubMed ID: 1338769
[TBL] [Abstract][Full Text] [Related]
20. Why is there no diploid overdose effect in Prader-Willi syndrome due to uniparental disomy?
Smith A
Acta Genet Med Gemellol (Roma); 1996; 45(1-2):179-89. PubMed ID: 8872029
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
