199 related articles for article (PubMed ID: 2750788)
1. Quantitative calibration and use of DNA probes for investigating chromosome abnormalities in the Prader-Willi syndrome.
Tantravahi U; Nicholls RD; Stroh H; Ringer S; Neve RL; Kaplan L; Wharton R; Wurster-Hill D; Graham JM; Cantú ES
Am J Med Genet; 1989 May; 33(1):78-87. PubMed ID: 2750788
[TBL] [Abstract][Full Text] [Related]
2. Restriction fragment length polymorphisms within proximal 15q and their use in molecular cytogenetics and the Prader-Willi syndrome.
Nicholls RD; Knoll JH; Glatt K; Hersh JH; Brewster TD; Graham JM; Wurster-Hill D; Wharton R; Latt SA
Am J Med Genet; 1989 May; 33(1):66-77. PubMed ID: 2568752
[TBL] [Abstract][Full Text] [Related]
3. Detection of molecular rearrangements in Prader-Willi syndrome patients by using genomic probes recognizing four loci within the PWCR.
Gregory CA; Kirkilionis AJ; Greenberg CR; Chudley AE; Hamerton JL
Am J Med Genet; 1990 Apr; 35(4):536-45. PubMed ID: 1970703
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Molecular study of the Prader-Willi syndrome: deletion, RFLP, and phenotype analyses of 50 patients.
Hamabe J; Fukushima Y; Harada N; Abe K; Matsuo N; Nagai T; Yoshioka A; Tonoki H; Tsukino R; Niikawa N
Am J Med Genet; 1991 Oct; 41(1):54-63. PubMed ID: 1683159
[TBL] [Abstract][Full Text] [Related]
6. Difference in methylation patterns within the D15S9 region of chromosome 15q11-13 in first cousins with Angelman syndrome and Prader-Willi syndrome.
Clayton-Smith J; Driscoll DJ; Waters MF; Webb T; Andrews T; Malcolm S; Pembrey ME; Nicholls RD
Am J Med Genet; 1993 Oct; 47(5):683-6. PubMed ID: 8266996
[TBL] [Abstract][Full Text] [Related]
7. Prader-Willi syndrome resulting from an unbalanced translocation: characterization by array comparative genomic hybridization.
Klein OD; Cotter PD; Albertson DG; Pinkel D; Tidyman WE; Moore MW; Rauen KA
Clin Genet; 2004 Jun; 65(6):477-82. PubMed ID: 15151506
[TBL] [Abstract][Full Text] [Related]
8. Prenatal diagnosis of chromosome 15 abnormalities in the Prader-Willi/Angelman syndrome region by traditional and molecular cytogenetics.
Toth-Fejel S; Magenis RE; Leff S; Brown MG; Comegys B; Lawce H; Berry T; Kesner D; Webb MJ; Olson S
Am J Med Genet; 1995 Feb; 55(4):444-52. PubMed ID: 7762584
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Prader-Willi syndrome with an unusually large 15q deletion due to an unbalanced translocation t(4;15).
Varela MC; Lopes GM; Koiffmann CP
Ann Genet; 2004; 47(3):267-73. PubMed ID: 15337472
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Duplication of proximal 15q as a cause of Prader-Willi syndrome.
Pettigrew AL; Gollin SM; Greenberg F; Riccardi VM; Ledbetter DH
Am J Med Genet; 1987 Dec; 28(4):791-802. PubMed ID: 3688017
[TBL] [Abstract][Full Text] [Related]
13. Duplication within chromosome region 15q11-q13 in a patient with similarities to Prader-Willi syndrome confirmed by region-specific and band-specific fish.
Engelen JJ; Loots WJ; Albrechts JC; Schrander-Stumpel CT; Dirckx R; Smeets HJ; Hamers AJ; Geraedts JP
Genet Couns; 1999; 10(2):123-32. PubMed ID: 10422004
[TBL] [Abstract][Full Text] [Related]
14. A variety of genetic mechanisms are associated with the Prader-Willi syndrome.
Woodage T; Deng ZM; Prasad M; Smart R; Lindeman R; Christian SL; Ledbetter DH; Robson L; Smith A; Trent RJ
Am J Med Genet; 1994 Sep; 54(3):219-26. PubMed ID: 7810579
[TBL] [Abstract][Full Text] [Related]
15. Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation.
Saitoh S; Buiting K; Cassidy SB; Conroy JM; Driscoll DJ; Gabriel JM; Gillessen-Kaesbach G; Glenn CC; Greenswag LR; Horsthemke B; Kondo I; Kuwajima K; Niikawa N; Rogan PK; Schwartz S; Seip J; Williams CA; Nicholls RD
Am J Med Genet; 1997 Jan; 68(2):195-206. PubMed ID: 9028458
[TBL] [Abstract][Full Text] [Related]
16. Deletion of small nuclear ribonucleoprotein polypeptide N (SNRPN) in Prader-Willi syndrome detected by fluorescence in situ hybridization: two sibs with the typical phenotype without a cytogenetic deletion in chromosome 15q.
Ishikawa T; Kibe T; Wada Y
Am J Med Genet; 1996 Apr; 62(4):350-2. PubMed ID: 8723064
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Deletions and duplications of the 15q11-q13 region in spermatozoa from Prader-Willi syndrome fathers.
Molina O; Blanco J; Vidal F
Mol Hum Reprod; 2010 May; 16(5):320-8. PubMed ID: 20083560
[TBL] [Abstract][Full Text] [Related]
20. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.
Depienne C; Moreno-De-Luca D; Heron D; Bouteiller D; Gennetier A; Delorme R; Chaste P; Siffroi JP; Chantot-Bastaraud S; Benyahia B; Trouillard O; Nygren G; Kopp S; Johansson M; Rastam M; Burglen L; Leguern E; Verloes A; Leboyer M; Brice A; Gillberg C; Betancur C
Biol Psychiatry; 2009 Aug; 66(4):349-59. PubMed ID: 19278672
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
