Similar articles for PMID: 1969845

Year	Number of Results
1979	1
1983	1
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1986	1
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1989	4
1990	2
1991	9
1992	6
1993	7
1994	4
1995	4
1996	1
1997	4
1998	4
1999	4
2001	1
2003	1
2008	2
2013	1
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2015	1
2016	1
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2018	1
2024	0

1

The human homeobox gene HOX7 maps to chromosome 4p16.1 and may be implicated in Wolf-Hirschhorn syndrome.

Ivens A, Flavin N, Williamson R, Dixon M, Bates G, Buckingham M, Robert B. Ivens A, et al. Hum Genet. 1990 Apr;84(5):473-6. doi: 10.1007/BF00195823. Hum Genet. 1990. PMID: 1969845

2

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. Chen CP, et al. Taiwan J Obstet Gynecol. 2017 Dec;56(6):821-826. doi: 10.1016/j.tjog.2017.10.021. Taiwan J Obstet Gynecol. 2017. PMID: 29241927 Free article.

3

Congenital cavitary optic disc anomaly and Axenfeld's anomaly in Wolf-Hirschhorn syndrome: A case report and review of the literature.

Ali MH, Azar NF, Aakalu V, Chau FY, Abbasian J, Setabutr P, Maumenee IH. Ali MH, et al. Ophthalmic Genet. 2018 Apr;39(2):271-274. doi: 10.1080/13816810.2017.1408850. Epub 2017 Dec 4. Ophthalmic Genet. 2018. PMID: 29199884 Free PMC article. Review.

4

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. Yang WX, et al. Taiwan J Obstet Gynecol. 2016 Feb;55(1):104-8. doi: 10.1016/j.tjog.2015.12.006. Taiwan J Obstet Gynecol. 2016. PMID: 26927259 Free article.

5

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. Iype T, et al. BMC Med Genet. 2015 Nov 10;16:104. doi: 10.1186/s12881-015-0251-5. BMC Med Genet. 2015. PMID: 26554554 Free PMC article.

6

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. Zollino M, et al. Epilepsia. 2014 Jun;55(6):849-57. doi: 10.1111/epi.12617. Epub 2014 Apr 16. Epilepsia. 2014. PMID: 24738919 Free article.

7

Microarray analysis of unbalanced translocation in Wolf-Hirschhorn syndrome.

Dai Y, Yang J, Chen Y, Bao L, Cheng Q. Dai Y, et al. Pediatr Int. 2013 Jun;55(3):368-70. doi: 10.1111/j.1442-200X.2012.03684.x. Pediatr Int. 2013. PMID: 23782367

8

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. Zollino M, et al. Am J Med Genet C Semin Med Genet. 2008 Nov 15;148C(4):257-69. doi: 10.1002/ajmg.c.30190. Am J Med Genet C Semin Med Genet. 2008. PMID: 18932124 Review.

9

The terminal 760 kb region on 4p16 is unlikely to be the critical interval for growth delay in Wolf-Hirschhorn syndrome.

Zollino M, Murdolo M, Neri G. Zollino M, et al. J Med Genet. 2008 Aug;45(8):544. doi: 10.1136/jmg.2008.058370. J Med Genet. 2008. PMID: 18676804 No abstract available.

10

Selection on coding regions determined Hox7 genes evolution.

Fares MA, Bezemer D, Moya A, Marín I. Fares MA, et al. Mol Biol Evol. 2003 Dec;20(12):2104-12. doi: 10.1093/molbev/msg222. Epub 2003 Aug 29. Mol Biol Evol. 2003. PMID: 12949154

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