329 related articles for article (PubMed ID: 6336316)
1. 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]
2. 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]
3. Unique karyotypes in two patients with Prader-Willi syndrome.
Narahara K; Hiramoto K; Murakami M; Miyake S; Tsuji K; Yokoyama Y; Namba H; Ninomiya S; Murakami R; Seino Y
Am J Med Genet; 1992 Mar; 42(5):671-7. PubMed ID: 1632436
[TBL] [Abstract][Full Text] [Related]
4. The Prader-Willi syndrome and interstitial deletion of chromosome 15: high-resolution chromosome analyses of 14 patients with the Prader-Willi syndrome and of 5 suspected infants.
Fukushima Y; Niikawa N; Kuroki Y
Jinrui Idengaku Zasshi; 1984 Mar; 29(1):1-6. PubMed ID: 6748325
[No Abstract] [Full Text] [Related]
5. Deletion of chromosome 15pter-->q11.2 due to t(Y;15) in a boy with Prader-Willi syndrome.
Qumsiyeh MB; Dalton JD; Gordon PL; Wilroy RS; Tharapel AT
Am J Med Genet; 1992 Jan; 42(1):109-11. PubMed ID: 1308348
[TBL] [Abstract][Full Text] [Related]
6. [A jumping translocation (5p;15q), (8q;15q), and (12q;15q) (author's transl)].
Lejeune J; Maunoury C; Prieur M; Van den Akker J
Ann Genet; 1979; 22(4):210-3. PubMed ID: 317782
[TBL] [Abstract][Full Text] [Related]
7. [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]
8. Prader-Willi syndrome.
Cassidy SB; Ledbetter DH
Neurol Clin; 1989 Feb; 7(1):37-54. PubMed ID: 2646521
[TBL] [Abstract][Full Text] [Related]
9. Molecular markers for diagnosis of Prader-Willi syndrome in thai patients by fish.
Wiriyaukaradecha S; Patmasiriwat P; Wasant P; Tantiniti P
Southeast Asian J Trop Med Public Health; 2003 Dec; 34(4):881-6. PubMed ID: 15115105
[TBL] [Abstract][Full Text] [Related]
10. Deletions of proximal 15q and non-classical Prader-Willi syndrome phenotypes.
Schwartz S; Max SR; Panny SR; Cohen MM
Am J Med Genet; 1985 Feb; 20(2):255-63. PubMed ID: 2858158
[TBL] [Abstract][Full Text] [Related]
11. A case of Prader Willi syndrome with del 15 (q11-->q13).
Tunçman G; Tükün A; Yalaz K; Bökesoy I
Turk J Pediatr; 1993; 35(4):333-6. PubMed ID: 8160287
[TBL] [Abstract][Full Text] [Related]
12. Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?
Kousseff BG; Diamond T; Essig Y; Miller K; Tedesco T
Am J Med Genet; 1987 Dec; 28(4):803-11. PubMed ID: 3688018
[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. Comparison of high resolution chromosome banding and fluorescence in situ hybridization (FISH) for the laboratory evaluation of Prader-Willi syndrome and Angelman syndrome.
Delach JA; Rosengren SS; Kaplan L; Greenstein RM; Cassidy SB; Benn PA
Am J Med Genet; 1994 Aug; 52(1):85-91. PubMed ID: 7977469
[TBL] [Abstract][Full Text] [Related]
15. Interstitial 6q deletion with a Prader-Willi-like phenotype: a new case and review of the literature.
Gilhuis HJ; van Ravenswaaij CM; Hamel BJ; Gabreëls FJ
Eur J Paediatr Neurol; 2000; 4(1):39-43. PubMed ID: 10701104
[TBL] [Abstract][Full Text] [Related]
16. [High-resolution cytogenetic study of a patient with Prader-Willi syndrome].
Shi Y
Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Jun; 15(3):217-20. PubMed ID: 8222009
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. The Prader-Willi syndrome: a study of 40 patients and a review of the literature.
Bray GA; Dahms WT; Swerdloff RS; Fiser RH; Atkinson RL; Carrel RE
Medicine (Baltimore); 1983 Mar; 62(2):59-80. PubMed ID: 6338343
[TBL] [Abstract][Full Text] [Related]
19. [Chromosome aberrations in Prader-Willi-Labhart syndrome--critical review, documented by 4 unusual cases].
Pfeiffer RA; Tschech L; Irle U; Wündisch GF
Klin Padiatr; 1987; 199(5):329-35. PubMed ID: 3316824
[TBL] [Abstract][Full Text] [Related]
20. Deletions of proximal 15q without Prader-Willi syndrome.
Greenberg F; Ledbetter DH
Am J Med Genet; 1987 Dec; 28(4):813-20. PubMed ID: 3688019
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
