154 related articles for article (PubMed ID: 2730469)
1. A survey of 22 individuals with Prader-Willi syndrome in New South Wales.
Gavranich J; Selikowitz M
Aust Paediatr J; 1989 Feb; 25(1):43-6. PubMed ID: 2730469
[TBL] [Abstract][Full Text] [Related]
2. The changing purpose of Prader-Willi syndrome clinical diagnostic criteria and proposed revised criteria.
Gunay-Aygun M; Schwartz S; Heeger S; O'Riordan MA; Cassidy SB
Pediatrics; 2001 Nov; 108(5):E92. PubMed ID: 11694676
[TBL] [Abstract][Full Text] [Related]
3. Expression of 4 genes between chromosome 15 breakpoints 1 and 2 and behavioral outcomes in Prader-Willi syndrome.
Bittel DC; Kibiryeva N; Butler MG
Pediatrics; 2006 Oct; 118(4):e1276-83. PubMed ID: 16982806
[TBL] [Abstract][Full Text] [Related]
4. Early diagnosis of Prader-Willi syndrome in a newborn.
Chen CJ; Hsu ML; Yuh YS; Cheng SN; Kuo PL; Lee CM
Acta Paediatr Taiwan; 2004; 45(2):108-10. PubMed ID: 15335123
[TBL] [Abstract][Full Text] [Related]
5. Pure distal monosomy 10q26 in a patient displaying clinical features of Prader-Willi syndrome during infancy and distinct behavioural phenotype in adolescence.
Lukusa T; Fryns JP
Genet Couns; 2000; 11(2):119-26. PubMed ID: 10893663
[TBL] [Abstract][Full Text] [Related]
6. Neonatal diagnosis of Prader-Willi syndrome and its implications.
Greenberg F; Elder FF; Ledbetter DH
Am J Med Genet; 1987 Dec; 28(4):845-56. PubMed ID: 3688023
[TBL] [Abstract][Full Text] [Related]
7. Psychological profile and behavioural characteristics in 12 patients with Prader-Willi syndrome.
Borghgraef M; Fryns JP; Van Den Berghe H
Genet Couns; 1990; 1(2):141-50. PubMed ID: 1706926
[TBL] [Abstract][Full Text] [Related]
8. Severe neonatal-onset panniculitis in a female infant with Prader-Willi syndrome.
Sakthivel M; Hughes SM; Riley P; Arkwright PD; Mukherjee A; Ramsden S; Urquhart J; Crow YJ
Am J Med Genet A; 2011 Dec; 155A(12):3087-9. PubMed ID: 22052851
[TBL] [Abstract][Full Text] [Related]
9. The neonatal presentation of Prader-Willi syndrome revisited.
Miller SP; Riley P; Shevell MI
J Pediatr; 1999 Feb; 134(2):226-8. PubMed ID: 9931534
[TBL] [Abstract][Full Text] [Related]
10. Comparison of high resolution cytogenetics, fluorescence in situ hybridisation, and DNA studies to validate the diagnosis of Prader-Willi and Angelman's syndromes.
Smith A; Prasad M; Deng ZM; Robson L; Woodage T; Trent RJ
Arch Dis Child; 1995 May; 72(5):397-402. PubMed ID: 7618904
[TBL] [Abstract][Full Text] [Related]
11. Prader-Willi syndrome: clinical and molecular cytogenetic investigations.
Hou JW; Wang TR
J Formos Med Assoc; 1996 Jun; 95(6):474-9. PubMed ID: 8772055
[TBL] [Abstract][Full Text] [Related]
12. Prader-Willi syndrome.
Cassidy SB; Ledbetter DH
Neurol Clin; 1989 Feb; 7(1):37-54. PubMed ID: 2646521
[TBL] [Abstract][Full Text] [Related]
13. [Cytogenetic detection of Prader-Willi syndrome in infancy].
Götz J; Krüger G; Westphal BC; Pelz L
Kinderarztl Prax; 1989 May; 57(5):239-43. PubMed ID: 2747122
[TBL] [Abstract][Full Text] [Related]
14. [Infant hypotonia, obesity, hypogenitalism and oligophrenia--new viewpoints on the etiology and symptoms of Prader-Willi syndrome].
Witkowski R; Ullrich E; Pietsch P; Weber K; Heller K; Losanowa T; Nitz I
Psychiatr Neurol Med Psychol (Leipz); 1985 May; 37(5):255-61. PubMed ID: 4023109
[TBL] [Abstract][Full Text] [Related]
15. Clinical correlates of chromosome 15 deletions and maternal disomy in Prader-Willi syndrome.
Lai LW; Erickson RP; Cassidy SB
Am J Dis Child; 1993 Nov; 147(11):1217-23. PubMed ID: 7901987
[TBL] [Abstract][Full Text] [Related]
16. Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome.
Butler MG; Kaler SG; Yu PL; Meaney FJ
Clin Genet; 1982 Dec; 22(6):315-20. PubMed ID: 7160103
[TBL] [Abstract][Full Text] [Related]
17. Deletion of chromosome 15 (q11-13) in a Prader-Labhart-Willi syndrome clinic population.
Cassidy SB; Thuline HC; Holm VA
Am J Med Genet; 1984 Feb; 17(2):485-95. PubMed ID: 6336316
[TBL] [Abstract][Full Text] [Related]
18. Neonatal presentation of Prader Willi sindrome. Personal records.
Maggio MC; Corsello M; Piccione M; Piro E; Giuffrè M; Liotta A
Minerva Pediatr; 2007 Dec; 59(6):817-23. PubMed ID: 17978792
[TBL] [Abstract][Full Text] [Related]
19. [Neonatal hypotonia in Prader-Willi syndrome due to t(15;16)].
Fernández-Novoa MC; Vargas MT; Santano MR; Moya J; Garnacho MC
Rev Neurol; 2000 Sep 1-15; 31(5):499-500. PubMed ID: 11027108
[No Abstract] [Full Text] [Related]
20. [Prader-Labhart-Willi syndrome in infants].
Schmeling H; Gillessen-Kaesbach G; Schulte-Mattler U; Burdach S; Horneff G
Klin Padiatr; 2002; 214(2):51-3. PubMed ID: 11972309
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
