Shirian S, Shahabinejad H, Saeedzadeh A, Daneshbod K, Khosropanah H,
Mortazavi M, Daneshbod Y. Zimmermann-Laband syndrome: Clinical and cytogenetic
study in two related patients. J Clin Exp Dent. 2019;11(5):e452-6.
doi:10.4317/jced.55214
http://dx.doi.org/10.4317/jced.55214
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References
1. Chadwick B, Hunter B,
Hunter L, Aldred M, Wilkie A. Laband syndrome. Report of two cases, review of
the literature, and identification of additional manifestations. Oral Surg
Oral Med Oral Pathol. 1994:78:57-63. |
|
|
|
2. Sattur AP, Burde KN,
Nailmasur VG, Goyal M. Zimmermann-Laband syndrome: Report of a Case with
early cardiac complications. Journal of Indian Academy of Oral Medicine and
Radiology. 2010;22:174-176. |
|
|
|
3. Castori M, Valiante M,
Pascolini G, Leuzzi V, Pizzuti A, Grammatico P. Clinical and genetic study of
two patients with ZimmermanneLaband syndrome and literature review. Eur J Med
Genet. 2013;56:570-576 |
|
|
|
4. Crotwell PL, Hoyme HE.
Advances in whole-genome genetic testing: from chromosomes to microarrays.
Curr Probl Pediatr Adolesc Health Care. 2012;42:47-73. |
|
|
|
5. Bartsch O, Schindler D,
Beyer V, Gesk S, van't Slot R, Feddersen I, et al. A girl with an atypical
form of ataxia telangiectasia and an additional de novo 3.14 Mb
microduplication in region19q12. Eur J Med Genet. 2012;55:49-55. |
|
|
|
6. Lin, Z., et al., Report
of a case of Zimmermann-Laband syndrome with new manifestations. Int J Oral
Maxillofac Surg, 2010;39:937-41. |
|
|
|
7. Kim HG, Higgins AW,
Herrick SR, Kishikawa S, Nicholson L, Kutsche K, Ligon AH, Harris DJ,
MacDonald ME, Bruns GA, Morton CC, Quade BJ, Gusella JF. Candidate loci for
Zimmermann-Laband syndrome at 3p14.3. Am J Med Genet A. 2007;143A:107-11. |
|
|
|
8. Wynne SE, Aldred MJ,
Bartold PM. Hereditary gingival fibromatosis associated with hearing loss and
supernumerary teeth--a new syndrome. J Periodontol, 1995;66:75-9. |
|
|
|
9. Stefanova M, Atanassov D,
Krastev T, Fuchs S, Kutsche K. Zimmermanne Laband syndrome associated with a
balanced reciprocal translocation t(3;8)(p21.2;q24.3)
in mother and daughter: molecular cytogenetic characterization of the breakpoint
regions. Am J Med Genet. 2003;117A:289-294. |
|
|
|
10. Hoogendijk CF, Marx J,
Honey EM, Pretorius E, Christianson AL. Ultrastructural investigation of
Zimmermann-Laband syndrome. Ultrastruct Pathol. 2006;30:423-426. |
|
|
|
11. Hu P, Wang Y, Meng LL,
Qin L, Ma DY, Yi L, et al. 1q25.2-q31.3 Deletion in a female with mental
retardation, clinodactyly, minor facial anomalies but no growth retardation.
Mol Cytogenet. 2013;6:30. |
|
|
|
12. Schinzel A. Possible
trisomy 1q25 leads to 1q32 in a malformed girl with a de novo insertion in
1q. Hum
Genet. 1979;49:167-73. |
|
|
|
13. Warden CR, Pillers DA,
Rice MJ, Wildes J, Livingston JS, Clark BA, et al. Interstitial duplication
of the short arm of chromosome 1 in a newborn with congenital heart disease
and multiple malformations. Am J Med Genet. 2001;101:100-105. |
|
|
|
14. O'Driscoll M, Jeggo P.
The role of double-strand break repair e insights from human genetics, Nat
Rev Genet 2006;7:45-54. |
|
|
|
15. Couteau F, Zetka M. DNA
damage during meiosis induces chromatin remodeling and synaptonemal complex
disassembly. Dev
Cell 2011;20:353-363. |
|
|
|
16. Kloosterman WP, Guryev
V, van Roosmalen M, Duran KJ, de Bruijn E, Bakker SC, et al. Chromothripsis
as a mechanism driving complex de novo structural rearrangements in the
germline. Hum
Mol Genet. 2011;20:1916-1924. |