154 related articles for article (PubMed ID: 7398114)
1. A new case of rearrangement of chromosome 15 associated with Prader Willi syndrome.
Guanti G
Clin Genet; 1980 Jun; 17(6):423-7. PubMed ID: 7398114
[TBL] [Abstract][Full Text] [Related]
2. [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]
3. 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
[TBL] [Abstract][Full Text] [Related]
4. Unbalanced reciprocal translocations in cases of Prader-Willi syndrome.
Duckett DP; Roberts SH; Davies P
Hum Genet; 1984; 67(2):156-61. PubMed ID: 6336319
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Translocations in Prader-Willi syndrome.
Charrow J; Balkin N; Cohen MM
Clin Genet; 1983 Apr; 23(4):304-7. PubMed ID: 6851221
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Duplication in chromosome 15q in a boy with the Prader-Willi syndrome; further cytogenetic confusion.
de France HF; Beemer FA; Ippel PF
Clin Genet; 1984 Oct; 26(4):379-82. PubMed ID: 6499252
[TBL] [Abstract][Full Text] [Related]
10. De novo (15;21) unbalanced translocation of paternal origin in a girl with Prader-Willi syndrome.
Cuoco C; Bicocchi MP; Granata D; Mezzano P; Serra G
Am J Med Genet; 1990 Sep; 37(1):62-4. PubMed ID: 2240045
[TBL] [Abstract][Full Text] [Related]
11. [Prader-Willi syndrome and translocation 15/15].
Tylki A; Lech H; Gurkau M; Parcheta B
Ann Genet; 1982; 25(3):183-4. PubMed ID: 6982673
[No Abstract] [Full Text] [Related]
12. A male with a de novo translocation involving loss of 15q11q13 material and Prader-Willi syndrome.
Vickers S; Dahlitz M; Hardy C; Kilpatrick M; Webb T
J Med Genet; 1994 Jun; 31(6):478-81. PubMed ID: 8071975
[TBL] [Abstract][Full Text] [Related]
13. A 15/17 translocation in a patient with Prader-Labhart-Willi syndrome.
Cavalli IJ; Sbalqueiro IJ; Wajntal A; Freire-Maia N
Hum Hered; 1982; 32(3):149-51. PubMed ID: 7106779
[No Abstract] [Full Text] [Related]
14. Microdeletion 15q26.2qter and Microduplication 18q23 in a Patient with Prader-Willi-Like Syndrome: Clinical Findings.
Dello Russo P; Demori E; Sechi A; Passon N; Romagno D; Gnan C; Zoratti R; Damante G
Cytogenet Genome Res; 2016; 148(1):14-8. PubMed ID: 27160288
[TBL] [Abstract][Full Text] [Related]
15. Chromosome 15 anomalies and the Prader-Willi syndrome: cytogenetic analysis.
Mattei MG; Souiah N; Mattei JF
Hum Genet; 1984; 66(4):313-34. PubMed ID: 6373566
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Trisomy 9p and Prader-Willi syndromes in an infant resulting from a de-novo unbalanced t(9;15) translocation.
Carter MT; Jacob FD; Sinclair-Bourque E; Ray R; Allanson JE
Clin Dysmorphol; 2009 Apr; 18(2):103-106. PubMed ID: 19282755
[TBL] [Abstract][Full Text] [Related]
18. Cytogenetic studies of familial Prader-Willi syndrome.
Hasegawa T; Hara M; Ando M; Osawa M; Fukuyama Y; Takahashi M; Yamada K
Hum Genet; 1984; 65(4):325-30. PubMed ID: 6693121
[TBL] [Abstract][Full Text] [Related]
19. A de novo unbalanced reciprocal translocation identified as paternal in origin in the Prader-Willi syndrome.
Smith A; Lindeman R; Volpato F; Kearney A; White S; Haan E; Trent RJ
Hum Genet; 1991 Mar; 86(5):534-6. PubMed ID: 2016095
[TBL] [Abstract][Full Text] [Related]
20. Microdissection of the Prader-Willi syndrome chromosome region and identification of potential gene sequences.
Buiting K; Neumann M; Lüdecke HJ; Senger G; Claussen U; Antich J; Passarge E; Horsthemke B
Genomics; 1990 Mar; 6(3):521-7. PubMed ID: 2328991
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]