545 related articles for article (PubMed ID: 27287194)
1. 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]
2. 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]
3. Microarray and FISH-based genotype-phenotype analysis of 22 Japanese patients with Wolf-Hirschhorn syndrome.
Shimizu K; Wakui K; Kosho T; Okamoto N; Mizuno S; Itomi K; Hattori S; Nishio K; Samura O; Kobayashi Y; Kako Y; Arai T; Tsutomu OI; Kawame H; Narumi Y; Ohashi H; Fukushima Y
Am J Med Genet A; 2014 Mar; 164A(3):597-609. PubMed ID: 24357569
[TBL] [Abstract][Full Text] [Related]
4. A large Indian family with rearrangement of chromosome 4p16 and 3p26.3 and divergent clinical presentations.
Iype T; Alakbarzade V; Iype M; Singh R; Sreekantan-Nair A; Chioza BA; Mohapatra TM; Baple EL; Patton MA; Warner TT; Proukakis C; Kulkarni A; Crosby AH
BMC Med Genet; 2015 Nov; 16():104. PubMed ID: 26554554
[TBL] [Abstract][Full Text] [Related]
5. Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with Wolf-Hirschhorn syndrome.
Yang WX; Pan H; Wang ST; Li L; Wu HR; Qi Y
Taiwan J Obstet Gynecol; 2016 Feb; 55(1):104-8. PubMed ID: 26927259
[TBL] [Abstract][Full Text] [Related]
6. Chromosomal microarray testing identifies a 4p terminal region associated with seizures in Wolf-Hirschhorn syndrome.
Ho KS; South ST; Lortz A; Hensel CH; Sdano MR; Vanzo RJ; Martin MM; Peiffer A; Lambert CG; Calhoun A; Carey JC; Battaglia A
J Med Genet; 2016 Apr; 53(4):256-63. PubMed ID: 26747863
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones.
Chen CP; Chen CY; Chern SR; Wu PS; Chen SW; Lai ST; Chuang TY; Yang CW; Chen LF; Wang W
Taiwan J Obstet Gynecol; 2017 Dec; 56(6):821-826. PubMed ID: 29241927
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Co-occurrence of 4p16.3 deletions with both paternal and maternal duplications of 11p15: modification of the Wolf-Hirschhorn syndrome phenotype by genetic alterations predicted to result in either a Beckwith-Wiedemann or Russell-Silver phenotype.
South ST; Whitby H; Maxwell T; Aston E; Brothman AR; Carey JC
Am J Med Genet A; 2008 Oct; 146A(20):2691-7. PubMed ID: 18798325
[TBL] [Abstract][Full Text] [Related]
11. 109 kb deletion of chromosome 4p16.3 in a patient with mild phenotype of Wolf-Hirschhorn syndrome.
Okamoto N; Ohmachi K; Shimada S; Shimojima K; Yamamoto T
Am J Med Genet A; 2013 Jun; 161A(6):1465-9. PubMed ID: 23637096
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. 4p16.1-p15.31 duplication and 4p terminal deletion in a 3-years old Chinese girl: Array-CGH, genotype-phenotype and neurological characterization.
Piccione M; Salzano E; Vecchio D; Ferrara D; Malacarne M; Pierluigi M; Ferrara I; Corsello G
Eur J Paediatr Neurol; 2015 Jul; 19(4):477-83. PubMed ID: 25769226
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Identification of a critical region on chromosome 4p16.3 for Wolf-Hirschhorn syndrome-associated fetal growth retardation].
Zheng W; Chen B; Yin Z; Huang X; Liang Y
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2020 Jul; 37(7):731-735. PubMed ID: 32619252
[TBL] [Abstract][Full Text] [Related]
16. A novel 4p16.3 microduplication distal to WHSC1 and WHSC2 characterized by oligonucleotide array with new phenotypic features.
Cyr AB; Nimmakayalu M; Longmuir SQ; Patil SR; Keppler-Noreuil KM; Shchelochkov OA
Am J Med Genet A; 2011 Sep; 155A(9):2224-8. PubMed ID: 21815251
[TBL] [Abstract][Full Text] [Related]
17. Segregation of a 4p16.3 duplication with a characteristic appearance, macrocephaly, speech delay and mild intellectual disability in a 3-generation family.
Schönewolf-Greulich B; Ravn K; Hamborg-Petersen B; Brøndum-Nielsen K; Tümer Z
Am J Med Genet A; 2013 Sep; 161A(9):2358-62. PubMed ID: 23894085
[TBL] [Abstract][Full Text] [Related]
18. On the nosology and pathogenesis of Wolf-Hirschhorn syndrome: genotype-phenotype correlation analysis of 80 patients and literature review.
Zollino M; Murdolo M; Marangi G; Pecile V; Galasso C; Mazzanti L; Neri G
Am J Med Genet C Semin Med Genet; 2008 Nov; 148C(4):257-69. PubMed ID: 18932124
[TBL] [Abstract][Full Text] [Related]
19. Microduplication of 4p16.3 due to an unbalanced translocation resulting in a mild phenotype.
Carmany EP; Bawle EV
Am J Med Genet A; 2011 Apr; 155A(4):819-24. PubMed ID: 21412978
[TBL] [Abstract][Full Text] [Related]
20. Prenatal Diagnosis and Molecular Cytogenetic Analyses of a de novo Deletion on Chromosome 4p16.3p15.33.
Luo H; Chang R; Liu F; Gao X
Altern Ther Health Med; 2023 Nov; 29(8):907-909. PubMed ID: 37708564
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
