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Journal Abstract Search
196 related items for PubMed ID: 6748325
1. 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]
7. [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 Mar; 22(4):210-3. PubMed ID: 317782 [Abstract] [Full Text] [Related]
8. 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 [Abstract] [Full Text] [Related]
11. Prader--Willi syndrome associated with an interstitial deletion of chromosome 15. Bonuccelli CM, Stetten G, Levitt RC, Levin LS, Pyeritz RE. Johns Hopkins Med J; 1982 Nov; 151(5):237-42. PubMed ID: 7143875 [No Abstract] [Full Text] [Related]
12. The Prader-Willi syndrome with a 15/3 translocation. Kucerová M, Straková M, Polívková Z. J Med Genet; 1979 Jun; 16(3):234-5. PubMed ID: 469905 [Abstract] [Full Text] [Related]
13. Unbalanced translocation (15;17)(q13;13.3) with apparent Prader-Willi syndrome but without Miller-Dieker syndrome. Elder FF, Nichols MM, Hood OJ, Harrison WR. Am J Med Genet; 1985 Mar; 20(3):519-24. PubMed ID: 3993677 [Abstract] [Full Text] [Related]
20. 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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]