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4. Prader-Willi syndrome and a deletion/duplication within the 15q11-q13 region. Butler MG; Bittel D; Talebizadeh Z J Med Genet; 2002 Mar; 39(3):202-4. PubMed ID: 11897825 [No Abstract] [Full Text] [Related]
5. [Molecular analysis in Prader-Willi syndrome diagnosis]. Szpecht-Potocka A Med Wieku Rozwoj; 1999; 3(3):407-19. PubMed ID: 10910667 [TBL] [Abstract][Full Text] [Related]
6. Approaches to the prenatal diagnosis of the Prader-Willi syndrome. Schinzel A Hum Genet; 1986 Nov; 74(3):327. PubMed ID: 3781563 [No Abstract] [Full Text] [Related]
7. [The use of molecular cytogenetic and cytogenetic techniques for the diagnosis of Prader-Willi and Angelman syndrome]. Iourov IY; Vorsanova SG; Kurinnaaya OS; Kolotii AD; Demidova IA; Kravets VS; Yurov YB Zh Nevrol Psikhiatr Im S S Korsakova; 2014; 114(1):49-53. PubMed ID: 24637817 [TBL] [Abstract][Full Text] [Related]
8. [Prader-Willi-Labhart syndrome: relations with the hypothalamus and chromosome 15]. Touraine P; Mbikay M; Seidah NG; Chrétien M Ann Endocrinol (Paris); 1990; 51(5-6):202-8. PubMed ID: 2130760 [TBL] [Abstract][Full Text] [Related]
9. Genetic testing for Prader-Willi and Angelman syndromes. Schad CR; Jalal SM; Thibodeau SN Mayo Clin Proc; 1995 Dec; 70(12):1195-6. PubMed ID: 7490922 [No Abstract] [Full Text] [Related]
10. Molecular screening for proximal 15q abnormalities in a mentally retarded population. Jacobsen J; King BH; Leventhal BL; Christian SL; Ledbetter DH; Cook EH J Med Genet; 1998 Jul; 35(7):534-8. PubMed ID: 9678696 [TBL] [Abstract][Full Text] [Related]
11. A multiplex molecular assay for the detection of uniparental disomy for human chromosome 15. Giardina E; Peconi C; Cascella R; Sinibaldi C; Nardone AM; Novelli G Electrophoresis; 2008 Dec; 29(23):4775-9. PubMed ID: 19053076 [TBL] [Abstract][Full Text] [Related]
12. Characterization of an autism-associated segmental maternal heterodisomy of the chromosome 15q11-13 region. Kwasnicka-Crawford DA; Roberts W; Scherer SW J Autism Dev Disord; 2007 Apr; 37(4):694-702. PubMed ID: 17006779 [TBL] [Abstract][Full Text] [Related]
13. [Unbalanced translocation t (5;15) in a patient with Prader-Willi syndrome]. Bai JL; Wang H; Yang YL; Song F Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Dec; 27(6):664-7. PubMed ID: 21154328 [TBL] [Abstract][Full Text] [Related]
15. The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13. Hogart A; Wu D; LaSalle JM; Schanen NC Neurobiol Dis; 2010 May; 38(2):181-91. PubMed ID: 18840528 [TBL] [Abstract][Full Text] [Related]
16. Prenatal diagnosis of Prader-Willi syndrome and Angelman syndrome for fetuses with suspicious deletion of chromosomal region 15q11-q13. Chang CW; Hsu HK; Kao CC; Huang JY; Kuo PL Int J Gynaecol Obstet; 2014 Apr; 125(1):18-21. PubMed ID: 24434231 [TBL] [Abstract][Full Text] [Related]
17. A combination of five short tandem repeats of chromosome 15 significantly improves the identification of Prader-Willi syndrome etiology in the Argentinean population. Aráoz HV; Torrado M; Barreiro C; Chertkoff L Genet Mol Res; 2006 Jun; 5(2):390-8. PubMed ID: 16819717 [TBL] [Abstract][Full Text] [Related]
18. Isochromosome 15q of maternal origin in two Prader-Willi syndrome patients previously diagnosed erroneously as cytogenetic deletions. Saitoh S; Mutirangura A; Kuwano A; Ledbetter DH; Niikawa N Am J Med Genet; 1994 Mar; 50(1):64-7. PubMed ID: 7909198 [TBL] [Abstract][Full Text] [Related]
19. Unique maternal deletion of 15q in a patient with some symptoms of Prader-Willi syndrome. Ninomiya S; Yokoyama Y; Kawakami M; Une T; Maruyama H; Morishima T Pediatr Int; 2005 Oct; 47(5):541-5. PubMed ID: 16190961 [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]