424 related articles for article (PubMed ID: 7815414)
1. Inv dup(15) supernumerary marker chromosomes.
Webb T
J Med Genet; 1994 Aug; 31(8):585-94. PubMed ID: 7815414
[No Abstract] [Full Text] [Related]
2. Clinical and molecular analysis of five inv dup(15) patients.
Robinson WP; Binkert F; Giné R; Vazquez C; Müller W; Rosenkranz W; Schinzel A
Eur J Hum Genet; 1993; 1(1):37-50. PubMed ID: 8069650
[TBL] [Abstract][Full Text] [Related]
3. Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.
Hou JW; Wang TR
Eur J Pediatr; 1998 Feb; 157(2):122-7. PubMed ID: 9504785
[TBL] [Abstract][Full Text] [Related]
4. Application of fluorescence in situ hybridization for early prenatal diagnosis of partial trisomy 6p/monosomy 6q due to a familial pericentric inversion.
Wauters JG; Bossuyt PJ; Roelen L; van Roy B; Dumon J
Clin Genet; 1993 Nov; 44(5):262-9. PubMed ID: 8313624
[TBL] [Abstract][Full Text] [Related]
5. FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation.
Cockwell AE; Dávalos IP; Rivera HR; Crolla JA
Am J Med Genet; 2001 Nov; 103(4):289-94. PubMed ID: 11746008
[TBL] [Abstract][Full Text] [Related]
6. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).
Battaglia A
Orphanet J Rare Dis; 2008 Nov; 3():30. PubMed ID: 19019226
[TBL] [Abstract][Full Text] [Related]
7. Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomes.
Abeliovich D; Dagan J; Werner M; Lerer I; Shapira Y; Meiner V
Eur J Hum Genet; 1995; 3(1):49-55. PubMed ID: 7767656
[TBL] [Abstract][Full Text] [Related]
8. Unique mosaicism in Prader-Labhart-Willi syndrome--a contiguous gene or aneuploidy syndrome?
Kousseff BG; Diamond T; Essig Y; Miller K; Tedesco T
Am J Med Genet; 1987 Dec; 28(4):803-11. PubMed ID: 3688018
[TBL] [Abstract][Full Text] [Related]
9. Application of fluorescence in situ hybridization to the identification of different marker chromosomes.
Verschraegen-Spae MR; Quack B; Rousseaux S; Pison H; Messiaen L; De Paepe A; Lespinasse J
Ann Genet; 1998; 41(1):5-10. PubMed ID: 9599644
[TBL] [Abstract][Full Text] [Related]
10. Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.
Leana-Cox J; Jenkins L; Palmer CG; Plattner R; Sheppard L; Flejter WL; Zackowski J; Tsien F; Schwartz S
Am J Hum Genet; 1994 May; 54(5):748-56. PubMed ID: 8178816
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.
Cheng SD; Spinner NB; Zackai EH; Knoll JH
Am J Hum Genet; 1994 Oct; 55(4):753-9. PubMed ID: 7942854
[TBL] [Abstract][Full Text] [Related]
14. Mosaic paternally derived inv dup(15) may partially rescue the Prader-Willi syndrome phenotype with uniparental disomy.
Saitoh S; Hosoki K; Takano K; Tonoki H
Clin Genet; 2007 Oct; 72(4):378-80. PubMed ID: 17850637
[No Abstract] [Full Text] [Related]
15. A supernumerary marker chromosome 15 tetrasomic for the Prader-Willi/Angelman syndrome critical region in a patient with a severe phenotype.
Maggouta F; Roberts SE; Dennis NR; Veltman MW; Crolla JA
J Med Genet; 2003 Jul; 40(7):e84. PubMed ID: 12843333
[No Abstract] [Full Text] [Related]
16. Developmental delay caused by a supernumerary chromosome, inv dup (15), identified by fluorescent in situ hybridization.
Abuelo D; Mark HF; Bier JA
Clin Pediatr (Phila); 1995 Apr; 34(4):223-6. PubMed ID: 7540523
[No Abstract] [Full Text] [Related]
17. 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]
18. Refined molecular characterization of the breakpoints in small inv dup(15) chromosomes.
Huang B; Crolla JA; Christian SL; Wolf-Ledbetter ME; Macha ME; Papenhausen PN; Ledbetter DH
Hum Genet; 1997 Jan; 99(1):11-7. PubMed ID: 9003485
[TBL] [Abstract][Full Text] [Related]
19. Prenatal diagnosis of mosaic tetrasomy 5p.
Park JP; Barefoot KH; Ornvold K; Berg SZ; Dossu JR; Mohandas TK
Prenat Diagn; 2001 May; 21(5):351-3. PubMed ID: 11360274
[TBL] [Abstract][Full Text] [Related]
20. Prenatal molecular cytogenetic diagnosis of partial tetrasomy 10p due to neocentromere formation in an inversion duplication analphoid marker chromosome.
Levy B; Papenhausen P; Tepperberg J; Dunn T; Fallet S; Magid M; Kardon N; Hirschhorn K; Warburton P
Cytogenet Cell Genet; 2000; 91(1-4):165-70. PubMed ID: 11173851
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
