114 related articles for article (PubMed ID: 9738866)
1. Centric fission of chromosome 9 in a boy with trisomy 9p.
Concolino D; Cinti R; Moricca M; Andria G; Strisciuglio P
Am J Med Genet; 1998 Aug; 79(1):35-7. PubMed ID: 9738866
[TBL] [Abstract][Full Text] [Related]
2. Localization by FISH of centric fission breakpoints in a de novo trisomy 9p patient with i(9p) and t(9q;11p).
Petit P; Devriendt K; Vermeesch JR; Meireleire J; Fryns JP
Genet Couns; 1998; 9(3):215-21. PubMed ID: 9777345
[TBL] [Abstract][Full Text] [Related]
3. Two cases of 9p deletion syndrome and a case of partial trisomy 8 and partial monosomy 9p.
Okten G; Sezer O; Günes S; Küçüködük S; Oğur G
Genet Couns; 2009; 20(4):341-7. PubMed ID: 20162869
[TBL] [Abstract][Full Text] [Related]
4. Pure 9p trisomy derived from a terminal balanced unreciprocal translocation.
Brambila-Tapia AJ; Neira VA; Vásquez-Velásquez AI; Jimenez-Arredondo RE; Chávez-González EL; Picos-Cárdenas VJ; Fletes-Rayas AL; Figuera LE
Genet Couns; 2014; 25(3):289-97. PubMed ID: 25365851
[TBL] [Abstract][Full Text] [Related]
5. Two cases with partial trisomy 9p: molecular cytogenetic characterization and clinical follow-up.
Littooij AS; Hochstenbach R; Sinke RJ; van Tintelen P; Giltay JC
Am J Med Genet; 2002 Apr; 109(2):125-32. PubMed ID: 11977161
[TBL] [Abstract][Full Text] [Related]
6. Phenotypic and cytogenetic spectrum of 9p trisomy.
Temtamy SA; Kamel AK; Ismail S; Helmy NA; Aglan MS; El Gammal M; El Ruby M; Mohamed AM
Genet Couns; 2007; 18(1):29-48. PubMed ID: 17515299
[TBL] [Abstract][Full Text] [Related]
7. Trisomy 9p syndrome in two brothers: with new clinical findings and review of the literature.
Hacihanefioğlu S; Güven GS; Deviren A; Silahtaroğlu AN; Yosunvkaya Fenerci E; Ozkiliç A; Yüksel A
Genet Couns; 2002; 13(1):41-8. PubMed ID: 12017237
[TBL] [Abstract][Full Text] [Related]
8. Another rare case of a child with de novo terminal 9p deletion and co-existing interstitial 9p duplication: clinical findings and molecular cytogenetic study by array-CGH.
Kowalczyk M; Tomaszewska A; Podbioł-Palenta A; Constantinou M; Wawrzkiewicz-Witkowska A; Kowalski J; Kałużewski B; Zajączek S; Srebniak MI
Cytogenet Genome Res; 2013; 139(1):9-16. PubMed ID: 22965227
[TBL] [Abstract][Full Text] [Related]
9. Fluorescence in situ hybridization reveals trisomy 2q by insertion into 9p in hepatoblastoma.
Balogh E; Swanton S; Kiss C; Jakab ZS; Secker-Walker LM; Oláh E
Cancer Genet Cytogenet; 1998 Apr; 102(2):148-50. PubMed ID: 9546070
[TBL] [Abstract][Full Text] [Related]
10. Supernumerary chromosome inherited from a maternal balanced translocation leading to pure trisomy 9p.
Tihy F; Lemyre E; Dallaire L; Lemieux N
Am J Med Genet; 2000 Apr; 91(5):383-6. PubMed ID: 10767003
[TBL] [Abstract][Full Text] [Related]
11. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
Chen CP; Su YN; Chern SR; Hsu CY; Tsai FJ; Wu PC; Lee CC; Chen YT; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2011 Mar; 50(1):67-73. PubMed ID: 21482378
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication.
Chen CP; Lin CJ; Chern SR; Wu PS; Chen YN; Chen SW; Lee CC; Chen LF; Yang CW; Wang W
Taiwan J Obstet Gynecol; 2016 Aug; 55(4):596-601. PubMed ID: 27590390
[TBL] [Abstract][Full Text] [Related]
13. Maternal origin of a unique extra chromosome, der(9)(pter-->q13::q13-->q12:) in a girl with typical trisomy 9p syndrome.
Teraoka M; Narahara K; Yokoyama Y; Ninomiya S; Mizuta S; Une T; Seino Y
Am J Med Genet; 2001 Jul; 102(1):25-8. PubMed ID: 11471168
[TBL] [Abstract][Full Text] [Related]
14. Trisomy 9p resulting from de novo 9/15 translocation and a 9p isochromosome.
Sandig KR; Mücke J; Veit H
Hum Genet; 1979 Nov; 52(2):175-8. PubMed ID: 511173
[TBL] [Abstract][Full Text] [Related]
15. Pure and complete 12p trisomy due to a maternal centric fission of chromosome 12.
Cetin Z; Mihci E; Yakut S; Keser I; Karauzum SB; Luleci G
Am J Med Genet A; 2011 Feb; 155A(2):349-52. PubMed ID: 21271652
[TBL] [Abstract][Full Text] [Related]
16. Characterization of a Complex Chromosomal Rearrangement Involving a de novo Duplication of 9p and 9q and a Deletion of 9q.
Martín-De Saro MD; Valdés-Miranda JM; Plaza-Benhumea L; Pérez-Cabrera A; Gonzalez-Huerta LM; Guevara-Yañez R; Cuevas-Covarrubias SA
Cytogenet Genome Res; 2015; 147(2-3):124-9. PubMed ID: 26900692
[TBL] [Abstract][Full Text] [Related]
17. Molecular cytogenetic characterisation of the first familial case of partial 9p duplication (p22p24).
Haddad BR; Lin AE; Wyandt H; Milunsky A
J Med Genet; 1996 Dec; 33(12):1045-7. PubMed ID: 9004142
[TBL] [Abstract][Full Text] [Related]
18. Prenatal diagnosis and molecular cytogenetic characterization of a derivative chromosome der(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting as apparent isochromosome 18q in a fetus with holoprosencephaly.
Chen CP; Kuo YK; Su YN; Chern SR; Tsai FJ; Wu PC; Chen YT; Town DD; Wang W
Taiwan J Obstet Gynecol; 2011 Jun; 50(2):182-7. PubMed ID: 21791305
[TBL] [Abstract][Full Text] [Related]
19. Familial whole-arm translocations (1;19), (9;13), and (12;21): a review of 101 constitutional exchanges.
Vázquez-Cárdenas A; Vásquez-Velásquez AI; Barros-Núñez P; Mantilla-Capacho J; Rocchi M; Rivera H
J Appl Genet; 2007; 48(3):261-8. PubMed ID: 17666779
[TBL] [Abstract][Full Text] [Related]
20. [Trisomy 9p and clinical heterogeneity: case report of an unusual presentation].
Lengyel A; Kosik A; Pinti É; Lódi C; Tory K; Fekete G; Haltrich I
Orv Hetil; 2018 Nov; 159(47):1994-2000. PubMed ID: 30474384
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]