264 related articles for article (PubMed ID: 8291556)
1. Inverted duplication of chromosome 5p14p15.3 confirmed with in situ hybridization.
Zenger-Hain JL; Van Dyke DL; Wiktor A; Walker H; Feldman GL
Am J Med Genet; 1993 Dec; 47(8):1198-201. PubMed ID: 8291556
[TBL] [Abstract][Full Text] [Related]
2. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.
Harrison KJ; Teshima IE; Silver MM; Jay V; Unger S; Robinson WP; James A; Levin A; Chitayat D
Am J Med Genet; 1998 Sep; 79(2):103-7. PubMed ID: 9741467
[TBL] [Abstract][Full Text] [Related]
3. Molecular and cytogenetic characterization of 9p- abnormalities.
Teebi AS; Gibson L; McGrath J; Meyn MS; Breg WR; Yang-Feng TL
Am J Med Genet; 1993 May; 46(3):288-92. PubMed ID: 8488873
[TBL] [Abstract][Full Text] [Related]
4. A paternally derived inverted duplication of 7q with evidence of a telomeric deletion.
Stetten G; Charity LL; Kasch LM; Scott AF; Berman CL; Pressman E; Blakemore KJ
Am J Med Genet; 1997 Jan; 68(1):76-81. PubMed ID: 8986281
[TBL] [Abstract][Full Text] [Related]
5. Clinical and cytogenetic findings in seven cases of inverted duplication of 8p with evidence of a telomeric deletion using fluorescence in situ hybridization.
Guo WJ; Callif-Daley F; Zapata MC; Miller ME
Am J Med Genet; 1995 Sep; 58(3):230-6. PubMed ID: 8533823
[TBL] [Abstract][Full Text] [Related]
6. A patient with a de novo t (6;9) and an interstitial duplication of (9)(q21.2q22.1).
Mohrschladt MF; Bijlsma EK; Sluijter S; De Coo RF; Hoovers JM; Leschot NJ
Clin Dysmorphol; 1999 Jul; 8(3):211-4. PubMed ID: 10457857
[TBL] [Abstract][Full Text] [Related]
7. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
[TBL] [Abstract][Full Text] [Related]
8. Identification and molecular confirmation of a small chromosome 10q duplication [dir dup(10)(q24.2-->q24.3)] inherited from a mother mosaic for the abnormality.
Tonk V; Schneider NR; Delgado MR; Mao J; Schultz RA
Am J Med Genet; 1996 Jan; 61(1):16-20. PubMed ID: 8741911
[TBL] [Abstract][Full Text] [Related]
9. First clinical case of small de novo duplication of 19q (13.3-13.4) confirmed by FISH.
Bhat M; Morrison PJ; Getty A; McManus D; Tubman R; Nevin NC
Am J Med Genet; 2000 Mar; 91(3):201-3. PubMed ID: 10756343
[TBL] [Abstract][Full Text] [Related]
10. Precise mapping of a de novo duplication 18(q21-->q22) utilizing cytogenetic, biochemical, and molecular techniques.
Wolff DJ; Schwartz MF; Cohen MM; Schwartz S
Am J Med Genet; 1993 Jun; 46(5):520-3. PubMed ID: 8322813
[TBL] [Abstract][Full Text] [Related]
11. [Inverted duplication of the short arm of chromosome 8].
Rodríguez Martínez L; Jiménez Muñoz-Delgado N; Nieto C; Martínez Carrascal A; López Grondona F; Martínez Frías ML
An Esp Pediatr; 2001 Nov; 55(5):458-62. PubMed ID: 11696311
[TBL] [Abstract][Full Text] [Related]
12. Boy with an interstitial 1q (q31q41) duplication confirmed by fluorescent in situ hybridisation.
Sillén A; Wadelius C; Annerén G
Am J Med Genet; 1998 Nov; 80(2):163-8. PubMed ID: 9805135
[TBL] [Abstract][Full Text] [Related]
13. Cytogenetic and molecular identification of a de novo direct duplication of the long arm of chromosome 4(q21.3-->q31.3).
Jeziorowska A; Ciesla W; Houck GE; Yao XL; Harris MS; Truszczak B; Skorski M; Jakubowski L; Jenkins EC; Kaluzewski B
Am J Med Genet; 1993 Apr; 46(1):83-7. PubMed ID: 7684191
[TBL] [Abstract][Full Text] [Related]
14. Duplication of chromosome region 8p23.1-->p23.3: a benign variant?
Engelen JJ; Moog U; Evers JL; Dassen H; Albrechts JC; Hamers AJ
Am J Med Genet; 2000 Mar; 91(1):18-21. PubMed ID: 10751083
[TBL] [Abstract][Full Text] [Related]
15. 10p duplication characterized by fluorescence in situ hybridization.
Wiktor A; Feldman GL; Kratkoczki P; Ditmars DM; Van Dyke DL
Am J Med Genet; 1994 Sep; 52(3):315-8. PubMed ID: 7528972
[TBL] [Abstract][Full Text] [Related]
16. Characterization of a complex chromosomal rearrangement in a patient with a typical catlike cry and no other clinical findings of cri-du-chat syndrome.
Sreekantaiah C; Kronn D; Marinescu RC; Goldin B; Overhauser J
Am J Med Genet; 1999 Sep; 86(3):264-8. PubMed ID: 10482877
[TBL] [Abstract][Full Text] [Related]
17. Characterization of an inversion duplication of the short arm of chromosome 8 by fluorescent in situ hybridization.
Henderson KG; Dill FJ; Wood S
Am J Med Genet; 1992 Nov; 44(5):615-8. PubMed ID: 1481820
[TBL] [Abstract][Full Text] [Related]
18. Four new cases of inverted terminal duplication: a modified hypothesis of mechanism of origin.
Hoo JJ; Chao M; Szego K; Rauer M; Echiverri SC; Harris C
Am J Med Genet; 1995 Sep; 58(4):299-304. PubMed ID: 8533837
[TBL] [Abstract][Full Text] [Related]
19. De novo pericentric inversion of chromosome 4, inv(4)(p16q12) in a boy with piebaldism and mental retardation.
Ramadevi AR; Naik U; Dutta U; Srikanth ; Prabhakara K
Am J Med Genet; 2002 Nov; 113(2):190-2. PubMed ID: 12407711
[TBL] [Abstract][Full Text] [Related]
20. Duplication of chromosome region (16)(p11.2 --> p12.1) in a mother and daughter with mild mental retardation.
Engelen JJ; de Die-Smulders CE; Dirckx R; Verhoeven WM; Tuinier S; Curfs LM; Hamers AJ
Am J Med Genet; 2002 Apr; 109(2):149-53. PubMed ID: 11977164
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]