186 related articles for article (PubMed ID: 7767656)
21. Trisomy 15 rescue with jumping translocation of distal 15q in Prader-Willi syndrome.
Devriendt K; Petit P; Matthijs G; Vermeesch JR; Holvoet M; De Muelenaere A; Marynen P; Cassiman JJ; Fryns JP
J Med Genet; 1997 May; 34(5):395-9. PubMed ID: 9152837
[TBL] [Abstract][Full Text] [Related]
22. Two Prader-Willi/Angelman syndrome loci present in an isodicentric marker chromosome.
Luke S; Verma RS; Giridharan R; Conte RA; Macera MJ
Am J Med Genet; 1994 Jul; 51(3):232-3. PubMed ID: 7521122
[TBL] [Abstract][Full Text] [Related]
23. Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome.
Chen CP; Lin SP; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Town DD; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Oct; 55(5):728-732. PubMed ID: 27751425
[TBL] [Abstract][Full Text] [Related]
24. Duplication of chromosome 15 in the region 15q11-13 in a patient with developmental delay and ataxia with similarities to Angelman syndrome.
Clayton-Smith J; Webb T; Cheng XJ; Pembrey ME; Malcolm S
J Med Genet; 1993 Jun; 30(6):529-31. PubMed ID: 8326502
[TBL] [Abstract][Full Text] [Related]
25. Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis.
Kuwano A; Mutirangura A; Dittrich B; Buiting K; Horsthemke B; Saitoh S; Niikawa N; Ledbetter SA; Greenberg F; Chinault AC
Hum Mol Genet; 1992 Sep; 1(6):417-25. PubMed ID: 1363801
[TBL] [Abstract][Full Text] [Related]
26. Atypical Prader-Willi and 15q13.3 Microdeletion Syndromes in a Patient with an Unbalanced Translocation.
Colovati MES; Grossi BM; Nunes GD; Fock RA; Guedes DR; Melaragno MI; Cernach MCSP
Cytogenet Genome Res; 2019; 158(4):192-198. PubMed ID: 31394532
[TBL] [Abstract][Full Text] [Related]
27. The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.
Battaglia A; Gurrieri F; Bertini E; Bellacosa A; Pomponi MG; Paravatou-Petsotas M; Mazza S; Neri G
Neurology; 1997 Apr; 48(4):1081-6. PubMed ID: 9109904
[TBL] [Abstract][Full Text] [Related]
28. Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15--case report plus review of similar cases.
Liehr T; Brude E; Gillessen-Kaesbach G; König R; Mrasek K; von Eggeling F; Starke H
Eur J Med Genet; 2005; 48(2):175-81. PubMed ID: 16053909
[TBL] [Abstract][Full Text] [Related]
29. Dinucleotide repeat polymorphism at the D15S11 locus in the Angelman/Prader-Willi region (AS/PWS) of chromosome 15.
Mutirangura A; Kuwano A; Ledbetter SA; Chinault AC; Ledbetter DH
Hum Mol Genet; 1992 May; 1(2):139. PubMed ID: 1301155
[No Abstract] [Full Text] [Related]
30. Unbalanced translocation t(15;22) in "severe" Prader-Willi syndrome.
Smith A; Jauch A; St Heaps L; Robson L; Kearney B
Ann Genet; 2000; 43(3-4):125-30. PubMed ID: 11164193
[TBL] [Abstract][Full Text] [Related]
31. A familial balanced inverted insertion ins(15)(q15q13q11.2) producing Prader-Willi syndrome, Angelman syndrome and duplication of 15q11.2-q13 in a single family: Importance of differentiation from a paracentric inversion.
Collinson MN; Roberts SE; Crolla JA; Dennis NR
Am J Med Genet A; 2004 Apr; 126A(1):27-32. PubMed ID: 15039970
[TBL] [Abstract][Full Text] [Related]
32. Molecular characterisation of four cases of intrachromosomal triplication of chromosome 15q11-q14.
Ungaro P; Christian SL; Fantes JA; Mutirangura A; Black S; Reynolds J; Malcolm S; Dobyns WB; Ledbetter DH
J Med Genet; 2001 Jan; 38(1):26-34. PubMed ID: 11134237
[TBL] [Abstract][Full Text] [Related]
33. Molecular cytogenetic evidence for a common breakpoint in the largest inverted duplications of chromosome 15.
Wandstrat AE; Leana-Cox J; Jenkins L; Schwartz S
Am J Hum Genet; 1998 Apr; 62(4):925-36. PubMed ID: 9529335
[TBL] [Abstract][Full Text] [Related]
34. Two inv dup(15) chromosomes in a woman with repeated abortions.
Shim SH; Lee CH; Park YJ; Lee HJ; Park WI; Cho YH
Am J Med Genet; 2001 Dec; 104(4):303-6. PubMed ID: 11754065
[TBL] [Abstract][Full Text] [Related]
35. Prader-Willi, Angelman, and 15q11-q13 Duplication Syndromes.
Kalsner L; Chamberlain SJ
Pediatr Clin North Am; 2015 Jun; 62(3):587-606. PubMed ID: 26022164
[TBL] [Abstract][Full Text] [Related]
36. [Phenotypic and genetic analysis of an inv dup(15) case with a BP3:BP3 rearrangement].
Zhong F; Lan F; Zhang X; Lin Y; Lin Y; Yan A; Tu X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun; 34(3):402-405. PubMed ID: 28604965
[TBL] [Abstract][Full Text] [Related]
37. Paternally derived de novo interstitial duplication of proximal 15q in a patient with developmental delay.
Mohandas TK; Park JP; Spellman RA; Filiano JJ; Mamourian AC; Hawk AB; Belloni DR; Noll WW; Moeschler JB
Am J Med Genet; 1999 Feb; 82(4):294-300. PubMed ID: 10051161
[TBL] [Abstract][Full Text] [Related]
38. The inv dup(15) or idic(15) syndrome: a clinically recognisable neurogenetic disorder.
Battaglia A
Brain Dev; 2005 Aug; 27(5):365-9. PubMed ID: 16023554
[TBL] [Abstract][Full Text] [Related]
39. Nonreciprocal and jumping translocations of 15q1----qter in Prader-Willi syndrome.
Rivera H; Zuffardi O; Gargantini L
Am J Med Genet; 1990 Nov; 37(3):311-7. PubMed ID: 2260556
[TBL] [Abstract][Full Text] [Related]
40. Inherited DNA amplification of the proximal 15q region: cytogenetic and molecular studies.
Mignon C; Parente F; Stavropoulou C; Collignon P; Moncla A; Turc-Carel C; Mattei MG
J Med Genet; 1997 Mar; 34(3):217-22. PubMed ID: 9132493
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
