These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
271 related articles for article (PubMed ID: 3953677)
1. Clinical and cytogenetic survey of 39 individuals with Prader-Labhart-Willi syndrome. Butler MG; Meaney FJ; Palmer CG Am J Med Genet; 1986 Mar; 23(3):793-809. PubMed ID: 3953677 [TBL] [Abstract][Full Text] [Related]
2. Hypopigmentation: a common feature of Prader-Labhart-Willi syndrome. Butler MG Am J Hum Genet; 1989 Jul; 45(1):140-6. PubMed ID: 2741944 [TBL] [Abstract][Full Text] [Related]
3. 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]
4. Analysis of chromosome breakage in the Prader-Labhart-Willi syndrome. Butler MG; Jenkins BB Am J Med Genet; 1989 Apr; 32(4):514-9. PubMed ID: 2505618 [TBL] [Abstract][Full Text] [Related]
5. The cytogenetic controversy in the Prader-Labhart-Willi syndrome. Kousseff BG Am J Med Genet; 1982 Dec; 13(4):431-9. PubMed ID: 7158643 [TBL] [Abstract][Full Text] [Related]
6. Comparison of the 15q deletions in Prader-Willi and Angelman syndromes: specific regions, extent of deletions, parental origin, and clinical consequences. Magenis RE; Toth-Fejel S; Allen LJ; Black M; Brown MG; Budden S; Cohen R; Friedman JM; Kalousek D; Zonana J Am J Med Genet; 1990 Mar; 35(3):333-49. PubMed ID: 2309780 [TBL] [Abstract][Full Text] [Related]
8. An anthropometric study of 38 individuals with Prader-Labhart-Willi syndrome. Butler MG; Meaney FJ Am J Med Genet; 1987 Feb; 26(2):445-55. PubMed ID: 3812595 [TBL] [Abstract][Full Text] [Related]
9. Sister chromatid exchange analysis in the Prader-Labhart-Willi syndrome. Butler MG; Jenkins BB Am J Med Genet; 1987 Dec; 28(4):821-7. PubMed ID: 3688020 [TBL] [Abstract][Full Text] [Related]
10. Plasma immunoreactive beta-melanocyte stimulating hormone (lipotropin) levels in individuals with Prader-Labhart-Willi syndrome. Butler MG; Jenkins BB; Orth DN Am J Med Genet; 1987 Dec; 28(4):839-44. PubMed ID: 3688022 [TBL] [Abstract][Full Text] [Related]
11. Dermatoglyphic features in Prader-Willi syndrome with respect to chromosomal findings. Reed T; Butler MG Clin Genet; 1984 Apr; 25(4):341-6. PubMed ID: 6713710 [TBL] [Abstract][Full Text] [Related]
12. 'Expanded' Prader-Willi syndrome in a boy with an unusual 15q chromosome deletion. Pauli RM; Meisner LF; Szmanda RJ Am J Dis Child; 1983 Nov; 137(11):1087-9. PubMed ID: 6637912 [TBL] [Abstract][Full Text] [Related]
14. Metacarpophalangeal pattern profile analysis in Prader-Willi syndrome. A follow-up report on 38 cases. Butler MG; Meaney FJ Clin Genet; 1985 Jul; 28(1):27-30. PubMed ID: 4028497 [TBL] [Abstract][Full Text] [Related]
15. [Self-induced cutaneous lesions in Prader-Willi syndrome]. Plantin P; Milochau P; Broussine L; Blondin G Ann Dermatol Venereol; 1997; 124(5):390-2. PubMed ID: 9739896 [TBL] [Abstract][Full Text] [Related]
16. Can women with the Prader-Labhart-Willi syndrome (PLWS) reproduce? Does the deletion (15)(q 11-13) occur in individuals not affected with PLWS? Zellweger H Am J Med Genet; 1988 Mar; 29(3):669-72. PubMed ID: 3377010 [No Abstract] [Full Text] [Related]
17. 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]
18. Clinical and cytogenetic studies of the Prader-Willi syndrome: evidence of phenotype-karyotype correlation. Niikawa N; Ishikiriyama S Hum Genet; 1985; 69(1):22-7. PubMed ID: 3855404 [TBL] [Abstract][Full Text] [Related]
19. Comparison of phenotype between patients with Prader-Willi syndrome due to deletion 15q and uniparental disomy 15. Cassidy SB; Forsythe M; Heeger S; Nicholls RD; Schork N; Benn P; Schwartz S Am J Med Genet; 1997 Feb; 68(4):433-40. PubMed ID: 9021017 [TBL] [Abstract][Full Text] [Related]
20. Deficiency, transposition, and duplication of one 15q region may be alternatively associated with Prader-Willi (or a similar) syndrome. Analysis of seven cases after varying ascertainment. Fraccaro M; Zuffardi O; Bühler E; Schinzel A; Simoni G; Witkowski R; Bonifaci E; Caufin D; Cignacco G; Delendi N Hum Genet; 1983; 64(4):388-94. PubMed ID: 6618490 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]