455 related articles for article (PubMed ID: 18564498)
1. Boy with seizures (West syndrome) and distal 7q duplication syndrome due to an unbalanced 7q;9p translocation.
Tüysüz B; Demirel A; Uysal S; Beyer V; Bartsch O
Genet Couns; 2008; 19(1):29-35. PubMed ID: 18564498
[TBL] [Abstract][Full Text] [Related]
2. Small inherited terminal duplication of 7q with hydrocephalus, cleft palate, joint contractures, and severe hypotonia.
Morava E; Bartsch O; Czakó M; Frensel A; Kalscheuer V; Kárteszi J; Kosztolányi G
Clin Dysmorphol; 2003 Apr; 12(2):123-7. PubMed ID: 12868476
[TBL] [Abstract][Full Text] [Related]
3. Duplication of 7p21.2-->pter due to maternal 7p;21q translocation: implications for critical segment assignment in the 7p duplication syndrome.
Cai T; Yu P; Tagle DA; Xia J
Am J Med Genet; 1999 Oct; 86(4):305-11. PubMed ID: 10494083
[TBL] [Abstract][Full Text] [Related]
4. Spectral karyotyping and fluorescence in situ hybridization analysis of de novo partial trisomy 7p (7p21.2-->pter) and partial monosomy 12q (12q24.33-->qter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Huang JK; Lee CC; Wang W
Genet Couns; 2006; 17(1):57-63. PubMed ID: 16719278
[TBL] [Abstract][Full Text] [Related]
5. Distal monosomy 16p13.3/distal trisomy 2p24.2-pter: molecular-cytogenetic characterisation and phenotype.
Mach M; Windpassinger C; Wagner K; Kroisel PM; Petek E
Genet Couns; 2007; 18(1):9-16. PubMed ID: 17515297
[TBL] [Abstract][Full Text] [Related]
6. Translocation/duplication of 9p onto a duplicated 4q.
Rivera H; Figuera LE; Vasquez AI
Genet Couns; 1992; 3(4):201-3. PubMed ID: 1472355
[TBL] [Abstract][Full Text] [Related]
7. Clinical diagnosis of partial duplication 7q.
Bartsch O; Kalbe U; Ngo TK; Lettau R; Schwinger E
Am J Med Genet; 1990 Oct; 37(2):254-7. PubMed ID: 2248294
[TBL] [Abstract][Full Text] [Related]
8. Duplication 5q and deletion 9p due to a t(5;9)(q34;p23) in 2 cousins with features of Hunter-McAlpine syndrome and hypothyroidism.
Vásquez-Velásquez AI; García-Castillo HA; González-Mercado MG; Dávalos IP; Raca G; Xu X; Dwyer E; Rivera H
Cytogenet Genome Res; 2011; 132(4):233-8. PubMed ID: 21063078
[TBL] [Abstract][Full Text] [Related]
9. A report of a patient with duplication of 7p13-->pter and deletion of 2p23-->pter due to a maternal 2p;7p translocation.
Türköver BB; Sayar C; Toksoy G; Elçioğlu N
Turk J Pediatr; 2009; 51(2):174-9. PubMed ID: 19480332
[TBL] [Abstract][Full Text] [Related]
10. Additional chromosome in a child as a result of a balanced reciprocal translocation t(12;18)(p13;q12) in his mother's karyotype.
Lassota M; Przełozna B; Płodzien M; Bugno M; Wnuk M; Kotylak Z; Słota E
J Appl Genet; 2005; 46(4):419-21. PubMed ID: 16278518
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Complex rearrangement involving 9p deletion and duplication in a syndromic patient: genotype/phenotype correlation and review of the literature.
Recalcati MP; Bellini M; Norsa L; Ballarati L; Caselli R; Russo S; Larizza L; Giardino D
Gene; 2012 Jul; 502(1):40-5. PubMed ID: 22537675
[TBL] [Abstract][Full Text] [Related]
13. Partial trisomy 13q identified by sequential fluorescence in situ hybridization.
Rao VV; Carpenter NJ; Gucsavas M; Coldwell J; Say B
Am J Med Genet; 1995 Jul; 58(1):50-3. PubMed ID: 7573156
[TBL] [Abstract][Full Text] [Related]
14. Malformation syndrome of duplication 12q24.1 leads to qter.
Melnyk AR; Weiss L; Van Dyke DL; Jarvi P
Am J Med Genet; 1981; 10(4):357-65. PubMed ID: 7332029
[TBL] [Abstract][Full Text] [Related]
15. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
El-Ruby M; Hemly NA; Zaki MS
Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
[TBL] [Abstract][Full Text] [Related]
16. Trisomy of 8q22.3 approximately q23-qter following an unbalanced 1;8 translocation in a boy with multiple anomalies.
Ergun MA; Balci S; Konaç E; Kan D; Menevşe S; Bartsch O
Turk J Pediatr; 2004; 46(4):384-7. PubMed ID: 15641279
[TBL] [Abstract][Full Text] [Related]
17. Duplication of distal 19q: clinical report and review.
Boyd E; Grass FS; Parke JC; Knutson K; Stevenson RE
Am J Med Genet; 1992 Feb; 42(3):326-30. PubMed ID: 1536172
[TBL] [Abstract][Full Text] [Related]
18. Congenital glaucoma and Silver-Russell phenotype associated with partial trisomy 7q and monosomy 15q.
Kato R; Kishibayashi J; Shimokawa O; Harada N; Niikawa N; Matsumoto N
Am J Med Genet; 2001 Dec; 104(4):319-22. PubMed ID: 11754068
[TBL] [Abstract][Full Text] [Related]
19. Mosaic dup (9p) diagnosed by fluorescence in situ hybridization (FISH).
Petty EM; Gibson LH; Breg WR; Burns JP; Yang-Feng TL
Am J Med Genet; 1993 Mar; 45(6):770-3. PubMed ID: 8456860
[TBL] [Abstract][Full Text] [Related]
20. A severely mental and motor retarded boy with monosomy 9pter-->p22 trisomy 10q26-->qter due to paternal reciprocal translocation 46,XY,t(9;10)(p23;q26).
Akbas E; Polat S; Karakas-Celik S; Altintas ZM; Yildirim M; Yilgor E
Genet Couns; 2011; 22(4):417-23. PubMed ID: 22303803
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
