These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
234 related articles for article (PubMed ID: 23894085)
1. 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]
2. 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]
3. 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]
4. 7p22.1 microduplication syndrome: Clinical and molecular characterization of an adult case and review of the literature. Caselli R; Ballarati L; Vignoli A; Peron A; Recalcati MP; Catusi I; Larizza L; Giardino D Eur J Med Genet; 2015 Nov; 58(11):578-83. PubMed ID: 26297194 [TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
7. Duplication of AKT3 as a cause of macrocephaly in duplication 1q43q44. Wang D; Zeesman S; Tarnopolsky MA; Nowaczyk MJ Am J Med Genet A; 2013 Aug; 161A(8):2016-9. PubMed ID: 23794269 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. 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]
10. Pure interstitial duplication of chromosome 7q (7q31.2-->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and intellectual disability. Chen CP; Lin SP; Chern SR; Tsai FJ; Lee MS; Chen YJ; Wang W Genet Couns; 2011; 22(4):425-30. PubMed ID: 22303804 [TBL] [Abstract][Full Text] [Related]
11. Subtelomeric 6.7 Mb trisomy 10p and 5.6 Mb monosomy 21q detected by FISH and array-CGH in three related patients. Szabó GP; Knegt AC; Ujfalusi A; Balogh E; Szabó T; Oláh É Am J Med Genet A; 2012 Apr; 158A(4):869-76. PubMed ID: 22407767 [TBL] [Abstract][Full Text] [Related]
12. A novel 5p15.33-14.1 deletion and 4q34.24-35.2 duplication in a patient with mental retardation, dysmorphic features and severe speech delay. Cao Q; Peng Y; Ge J; Zhang Y; Zhu J; Zhao L J Genet; 2014 Apr; 93(1):159-62. PubMed ID: 24840832 [No Abstract] [Full Text] [Related]
13. Genotype-phenotype correlation of deletions and duplications of 4p: case reports and literature review. Zhang X; Lu H; Yang H; Ji Y; Liu H; Liu W; Li J; Yang Z; Sun W Front Genet; 2023; 14():1174314. PubMed ID: 37388934 [TBL] [Abstract][Full Text] [Related]
14. Association of structural and numerical anomalies of chromosome 22 in a patient with syndromic intellectual disability. Naoufal R; Legendre M; Couet D; Gilbert-Dussardier B; Kitzis A; Bilan F; Harbuz R Eur J Med Genet; 2016 Sep; 59(9):483-7. PubMed ID: 27452446 [TBL] [Abstract][Full Text] [Related]
15. [Phenotypic and genetic analysis of a pedigree with 4p16 microduplication and 8p23 microdeletion]. Li C; Hou R; Liu C; Li LJ; Lyu Y Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2019 Oct; 36(10):989-992. PubMed ID: 31598942 [TBL] [Abstract][Full Text] [Related]
16. [Familial subtelomeric abnormality der(4)t(4p16.3;21q22.3) as a cause of mental retardation and mild dysmorphic features]. Obersztyn E; Klapecki J; Helias-Rodzewicz Z; Bocian E; Mazurczak T Med Wieku Rozwoj; 2006; 10(1 Pt 2):199-209. PubMed ID: 17028389 [TBL] [Abstract][Full Text] [Related]
17. 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]
18. Inherited duplication of the short arm of chromosome 18p11.32-p11.31 associated with developmental delay/intellectual disability. Balasubramanian M; Sithambaram S; Smith K Clin Dysmorphol; 2016 Jan; 25(1):19-22. PubMed ID: 26287558 [TBL] [Abstract][Full Text] [Related]
19. Delineating the Clinical Spectrum Associated With Xq25q26.2 Duplications: Report of 2 Families and Review of the Literature. Herriges JC; Arch EM; Burgio PA; Baldwin EE; LaGrave D; Lamb AN; Toydemir RM J Child Neurol; 2019 Feb; 34(2):86-93. PubMed ID: 30458662 [TBL] [Abstract][Full Text] [Related]
20. "Tandem" duplication of 4p16.1p16.3 chromosome region associated with 4p16.3pter molecular deletion resulting in Wolf-Hirschhorn syndrome phenotype. Zollino M; Wright TJ; Di Stefano C; Tosolini A; Battaglia A; Altherr MR; Neri G Am J Med Genet; 1999 Feb; 82(5):371-5. PubMed ID: 10069706 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]