216 related articles for article (PubMed ID: 19449429)
1. Inv dup del(4)(:p13-->p16.3::p16.3-->qter) in a girl without typical manifestations of Wolf-Hirschhorn syndrome.
Paskulin GA; Riegel M; Cotter PD; Kiss A; Rosa RF; Zen PR; Mombach R; Graziadio C
Am J Med Genet A; 2009 Jun; 149A(6):1302-7. PubMed ID: 19449429
[TBL] [Abstract][Full Text] [Related]
2. Inv dup del(4)(:p14 --> p16.3::p16.3 --> qter) with manifestations of partial duplication 4p and Wolf-Hirschhorn syndrome.
Kondoh Y; Toma T; Ohashi H; Harada N; Yoshiura K; Ohta T; Kishino T; Niikawa N; Matsumoto N
Am J Med Genet A; 2003 Jul; 120A(1):123-6. PubMed ID: 12794704
[TBL] [Abstract][Full Text] [Related]
3. Prenatal detection of a de novo terminal inverted duplication 4p in a fetus with the Wolf-Hirschhorn syndrome phenotype.
Beaujard MP; Jouannic JM; Bessières B; Borie C; Martin-Luis I; Fallet-Bianco C; Portnoï MF
Prenat Diagn; 2005 Jun; 25(6):451-5. PubMed ID: 15966060
[TBL] [Abstract][Full Text] [Related]
4. [Paternally originated Wolf-Hirschhorn syndrome detected by multiplex ligation-dependent probe amplification and microarray comparative genomic hybridization].
Zhu CJ; Huang ZY; Wu WQ; Zhao Q; Jiang HY; Xie JS
Zhonghua Er Ke Za Zhi; 2012 Jun; 50(6):460-4. PubMed ID: 22931946
[TBL] [Abstract][Full Text] [Related]
5. Unusual chromosomal mosaicism in Wolf-Hirschhorn syndrome: del(4)(p16)/der(4)(qter-q31.3::pter-qter).
Syrrou M; Borghgraef M; Fryns JP
Am J Med Genet; 2001 Dec; 104(3):199-203. PubMed ID: 11754044
[TBL] [Abstract][Full Text] [Related]
6. Loss of subtelomeric sequence associated with a terminal inversion duplication of the short arm of chromosome 4.
Cotter PD; Kaffe S; Li L; Gershin IF; Hirschhorn K
Am J Med Genet; 2001 Jul; 102(1):76-80. PubMed ID: 11471177
[TBL] [Abstract][Full Text] [Related]
7. Wolf-Hirschhorn (4p-) syndrome: prenatal diagnosis, molecular cytogenetic characterization and association with a 1.2-Mb microduplication at 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with an apparently pure 4p deletion.
Chen CP; Su YN; Chen YY; Su JW; Chern SR; Chen YT; Chen WL; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2011 Dec; 50(4):506-11. PubMed ID: 22212326
[TBL] [Abstract][Full Text] [Related]
8. Inv dup del(10q): identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements.
Chen CP; Chen M; Su YN; Huang JP; Ma GC; Chang SP; Chern SR; Chen YT; Su JW; Lee CC; Town DD; Wang W
Taiwan J Obstet Gynecol; 2012 Jun; 51(2):245-52. PubMed ID: 22795102
[TBL] [Abstract][Full Text] [Related]
9. Wolf-Hirschhorn syndrome: a case with normal karyotype, demonstrated by array CGH (aCGH).
Saberi A; Shariati G; Hamid M; Galehdari H; Abdorasouli N
Arch Iran Med; 2014 Sep; 17(9):642-4. PubMed ID: 25204484
[TBL] [Abstract][Full Text] [Related]
10. Submicroscopic duplication of the Wolf-Hirschhorn critical region with a 4p terminal deletion.
Roselló M; Monfort S; Orellana C; Ferrer-Bolufer I; Quiroga R; Oltra S; Martínez F
Cytogenet Genome Res; 2009; 125(2):103-8. PubMed ID: 19729912
[TBL] [Abstract][Full Text] [Related]
11. 4p16.3 microdeletions and microduplications detected by chromosomal microarray analysis: New insights into mechanisms and critical regions.
Bi W; Cheung SW; Breman AM; Bacino CA
Am J Med Genet A; 2016 Oct; 170(10):2540-50. PubMed ID: 27287194
[TBL] [Abstract][Full Text] [Related]
12. [Recombinant chromosome 4 with partial 4p deletion and 4q duplication inherited from paternal pericentric inversion].
Mun SJ; Cho EH; Chey MJ; Shim GH; Shin BM; Lee RK; Ko JK; Yoo SJ
Korean J Lab Med; 2010 Feb; 30(1):89-92. PubMed ID: 20197729
[TBL] [Abstract][Full Text] [Related]
13. A second case of inv(4)pat with both recombinants in the offspring: rec dup(4q) in a girl with Wolf-Hirschhorn syndrome and rec dup(4p).
Dufke A; Eggermann K; Balg S; Stengel-Rutkowski S; Enders H; Kaiser P
Cytogenet Cell Genet; 2000; 91(1-4):85-9. PubMed ID: 11173836
[TBL] [Abstract][Full Text] [Related]
14. Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delay.
Hannes F; Drozniewska M; Vermeesch JR; Haus O
Eur J Med Genet; 2010; 53(3):136-40. PubMed ID: 20197130
[TBL] [Abstract][Full Text] [Related]
15. Unusual 4p16.3 deletions suggest an additional chromosome region for the Wolf-Hirschhorn syndrome-associated seizures disorder.
Zollino M; Orteschi D; Ruiter M; Pfundt R; Steindl K; Cafiero C; Ricciardi S; Contaldo I; Chieffo D; Ranalli D; Acquafondata C; Murdolo M; Marangi G; Asaro A; Battaglia D
Epilepsia; 2014 Jun; 55(6):849-57. PubMed ID: 24738919
[TBL] [Abstract][Full Text] [Related]
16. Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16.
Zollino M; Lecce R; Murdolo M; Orteschi D; Marangi G; Selicorni A; Midro A; Sorge G; Zampino G; Memo L; Battaglia D; Petersen M; Pandelia E; Gyftodimou Y; Faravelli F; Tenconi R; Garavelli L; Mazzanti L; Fischetto R; Cavalli P; Savasta S; Rodriguez L; Neri G
Hum Genet; 2007 Dec; 122(5):423-30. PubMed ID: 17676343
[TBL] [Abstract][Full Text] [Related]
17. Comprehensive analysis of Wolf-Hirschhorn syndrome using array CGH indicates a high prevalence of translocations.
South ST; Whitby H; Battaglia A; Carey JC; Brothman AR
Eur J Hum Genet; 2008 Jan; 16(1):45-52. PubMed ID: 17726485
[TBL] [Abstract][Full Text] [Related]
18. Clinical, cytogenetic and molecular investigation in a fetus with Wolf-Hirschhorn syndrome with paternally derived 4p deletion. Case report and review of the literature.
Dietze I; Fritz B; Huhle D; Simoens W; Piecha E; Rehder H
Fetal Diagn Ther; 2004; 19(3):251-60. PubMed ID: 15067236
[TBL] [Abstract][Full Text] [Related]
19. Microarray analysis of unbalanced translocation in Wolf-Hirschhorn syndrome.
Dai Y; Yang J; Chen Y; Bao L; Cheng Q
Pediatr Int; 2013 Jun; 55(3):368-70. PubMed ID: 23782367
[TBL] [Abstract][Full Text] [Related]
20. De novo inv del(4) in an infant with the Wolf-Hirschhorn syndrome.
Serville F; Saura R; Billeaud C; Girard S; Choiset A; Longy M; Sandler B
Ann Genet; 1987; 30(3):170-4. PubMed ID: 3499855
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
