Similar articles for PMID: 24962056

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1

Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.

Vona B, Nanda I, Neuner C, Schröder J, Kalscheuer VM, Shehata-Dieler W, Haaf T. Vona B, et al. BMC Med Genet. 2014 Jun 25;15:72. doi: 10.1186/1471-2350-15-72. BMC Med Genet. 2014. PMID: 24962056 Free PMC article. Review.

2

Genotype-phenotype analysis of 4q deletion syndrome: proposal of a critical region.

Strehle EM, Yu L, Rosenfeld JA, Donkervoort S, Zhou Y, Chen TJ, Martinez JE, Fan YS, Barbouth D, Zhu H, Vaglio A, Smith R, Stevens CA, Curry CJ, Ladda RL, Fan ZJ, Fox JE, Martin JA, Abdel-Hamid HZ, McCracken EA, McGillivray BC, Masser-Frye D, Huang T. Strehle EM, et al. Am J Med Genet A. 2012 Sep;158A(9):2139-51. doi: 10.1002/ajmg.a.35502. Epub 2012 Jul 27. Am J Med Genet A. 2012. PMID: 22847869

3

Prenatal Diagnosis of 4q Terminal Deletion and Review of the Literature.

Tidrenczel Z, Tardy EP, Pikó H, Sarkadi E, Böjtös I, Demeter J, Simon J, Kósa JP, Beke A. Tidrenczel Z, et al. Cytogenet Genome Res. 2019;158(2):63-73. doi: 10.1159/000500735. Epub 2019 Jul 2. Cytogenet Genome Res. 2019. PMID: 31261151 Review.

4

4q34.1-q35.2 deletion in a boy with phenotype resembling 22q11.2 deletion syndrome.

Cuturilo G, Menten B, Krstic A, Drakulic D, Jovanovic I, Parezanovic V, Stevanovic M. Cuturilo G, et al. Eur J Pediatr. 2011 Nov;170(11):1465-70. doi: 10.1007/s00431-011-1533-3. Epub 2011 Jul 22. Eur J Pediatr. 2011. PMID: 21833498

5

Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype.

Sensi A, Prontera P, Buldrini B, Palma S, Aiello V, Gruppioni R, Calzolari E, Volinia S, Martini A. Sensi A, et al. Am J Med Genet A. 2008 Jan 1;146A(1):110-5. doi: 10.1002/ajmg.a.32059. Am J Med Genet A. 2008. PMID: 18074369

6

Chromosome 4q deletion syndrome: narrowing the cardiovascular critical region to 4q32.2-q34.3.

Xu W, Ahmad A, Dagenais S, Iyer RK, Innis JW. Xu W, et al. Am J Med Genet A. 2012 Mar;158A(3):635-40. doi: 10.1002/ajmg.a.34425. Epub 2012 Feb 2. Am J Med Genet A. 2012. PMID: 22302627 Free article.

7

20p12.3 deletion is rare cause of syndromic cleft palate: case report and review of literature.

Amasdl S, Natiq A, Sbiti A, Zerkaoui M, Lyahyai J, Amzazi S, Liehr T, Sefiani A. Amasdl S, et al. BMC Res Notes. 2016 Jan 2;9:5. doi: 10.1186/s13104-015-1828-y. BMC Res Notes. 2016. PMID: 26724919 Free PMC article. Review.

8

Molecular cytogenetic characterization of a 2q35-q37 duplication and a 4q35.1-q35.2 deletion in two cousins: a genotype-phenotype analysis.

Ronzoni L, Peron A, Bianchi V, Baccarin M, Guerneri S, Silipigni R, Lalatta F, Bedeschi MF. Ronzoni L, et al. Am J Med Genet A. 2015 Jul;167(7):1551-9. doi: 10.1002/ajmg.a.37063. Epub 2015 Apr 6. Am J Med Genet A. 2015. PMID: 25851921

9

Molecular cytogenetic analysis of a constitutional de novo interstitial deletion of chromosome 12p in a boy with developmental delay and congenital anomalies.

Gläser B, Rossier E, Barbi G, Chiaie LD, Blank C, Vogel W, Kehrer-Sawatzki H. Gläser B, et al. Am J Med Genet A. 2003 Jan 1;116A(1):66-70. doi: 10.1002/ajmg.a.10878. Am J Med Genet A. 2003. PMID: 12476454 Review.

10

A familial interstitial 4q35 deletion with no discernible clinical effects.

Yakut S, Clarck OA, Sanhal C, Nur BG, Mendilcioglu I, Karauzum SB, Cetin Z. Yakut S, et al. Am J Med Genet A. 2015 Aug;167A(8):1836-41. doi: 10.1002/ajmg.a.37097. Epub 2015 Apr 5. Am J Med Genet A. 2015. PMID: 25846895

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