39 related articles for article (PubMed ID: 11076044)
1. A 5-year-old white girl with Prader-Willi syndrome and a submicroscopic deletion of chromosome 15q11q13.
Butler MG; Christian SL; Kubota T; Ledbetter DH
Am J Med Genet; 1996 Oct; 65(2):137-41. PubMed ID: 8911606
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. INTRAFAMILIAL AND MIDPARENTAL-CHILD CORRELATIONS AND HERITABILITY ESTIMATES OF ANTHROPOMETRIC MEASUREMENTS IN PRADER-WILLI SYNDROME FAMILIES.
Butler MG; Haynes JL; Meaney FJ
Dysmorphol Clin Genet; 1990; 4(1):2-6. PubMed ID: 25505360
[TBL] [Abstract][Full Text] [Related]
4. Special clinical entity with 15q26 deletion: a novel case report.
Panteleev D; Sadova A; Pavlova G
J Genet; 2024; 103():. PubMed ID: 38831650
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Imprinted segments in the human genome: different DNA methylation patterns in the Prader-Willi/Angelman syndrome region as determined by the genomic sequencing method.
Zeschnigk M; Schmitz B; Dittrich B; Buiting K; Horsthemke B; Doerfler W
Hum Mol Genet; 1997 Mar; 6(3):387-95. PubMed ID: 9147641
[TBL] [Abstract][Full Text] [Related]
7. Three siblings with Prader-Willi syndrome caused by imprinting center microdeletions and review.
Hartin SN; Hossain WA; Weisensel N; Butler MG
Am J Med Genet A; 2018 Apr; 176(4):886-895. PubMed ID: 29437285
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. Submicroscopic deletion in cousins with Prader-Willi syndrome causes a grandmatrilineal inheritance pattern: effects of imprinting.
Ming JE; Blagowidow N; Knoll JH; Rollings L; Fortina P; McDonald-McGinn DM; Spinner NB; Zackai EH
Am J Med Genet; 2000 May; 92(1):19-24. PubMed ID: 10797418
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
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.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
14.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
15.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
