Similar articles for PMID: 26590955

Year	Number of Results
1986	1
1990	1
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1

Dual genetic diagnoses: Atypical hand-foot-genital syndrome and developmental delay due to de novo mutations in HOXA13 and NRXN1.

Wallis M, Tsurusaki Y, Burgess T, Borzi P, Matsumoto N, Miyake N, True D, Patel C. Wallis M, et al. Am J Med Genet A. 2016 Mar;170(3):717-24. doi: 10.1002/ajmg.a.37478. Epub 2015 Nov 21. Am J Med Genet A. 2016. PMID: 26590955

2

A missense mutation of HOXA13 underlies hand-foot-genital syndrome in a Chinese family.

Cao L, Chen C, Leng Y, Yan L, Wang S, Zhang X, Luo Y. Cao L, et al. J Genet. 2017 Sep;96(4):647-652. doi: 10.1007/s12041-017-0810-y. J Genet. 2017. PMID: 28947713 Free article.

3

Familial deletion of the HOXA gene cluster associated with Hand-Foot-Genital syndrome and phenotypic variability.

Tas E, Sebastian J, Madan-Khetarpal S, Sweet P, Yatsenko AN, Pollock N, Rajkovic A, Schneck FX, Yatsenko SA, Witchel SF. Tas E, et al. Am J Med Genet A. 2017 Jan;173(1):221-224. doi: 10.1002/ajmg.a.37981. Epub 2016 Sep 20. Am J Med Genet A. 2017. PMID: 27649277

4

Severe manifestations of hand-foot-genital syndrome associated with a novel HOXA13 mutation.

Imagawa E, Kayserili H, Nishimura G, Nakashima M, Tsurusaki Y, Saitsu H, Ikegawa S, Matsumoto N, Miyake N. Imagawa E, et al. Am J Med Genet A. 2014 Sep;164A(9):2398-402. doi: 10.1002/ajmg.a.36648. Epub 2014 Jun 16. Am J Med Genet A. 2014. PMID: 24934387

5

Novel HOXA13 mutations and the phenotypic spectrum of hand-foot-genital syndrome.

Goodman FR, Bacchelli C, Brady AF, Brueton LA, Fryns JP, Mortlock DP, Innis JW, Holmes LB, Donnenfeld AE, Feingold M, Beemer FA, Hennekam RC, Scambler PJ. Goodman FR, et al. Am J Hum Genet. 2000 Jul;67(1):197-202. doi: 10.1086/302961. Epub 2000 Jun 5. Am J Hum Genet. 2000. PMID: 10839976 Free PMC article.

6

Hand-foot-genital syndrome - analysis of two cases.

Piazza MJ, Urbanetz AA. Piazza MJ, et al. JBRA Assist Reprod. 2018 Jun 1;22(2):157-159. doi: 10.5935/1518-0557.20180025. JBRA Assist Reprod. 2018. PMID: 29638102 Free PMC article.

7

Hand-foot-genital syndrome with a 7p15 deletion: clinically recognizable syndrome.

Hosoki K, Ohta T, Fujita K, Nishigaki S, Shiomi M, Niikawa N, Saitoh S. Hosoki K, et al. Pediatr Int. 2012 Jun;54(3):e22-5. doi: 10.1111/j.1442-200X.2011.03550.x. Pediatr Int. 2012. PMID: 22631585 No abstract available.

8

[Hand-foot-genital syndrome].

Mitsubuchi H, Endo F. Mitsubuchi H, et al. Nihon Rinsho. 2006 Jun 28;Suppl 2:647-8. Nihon Rinsho. 2006. PMID: 16817484 Review. Japanese. No abstract available.

9

A novel mutation of HOXA13 in a family with hand-foot-genital syndrome and the role of polyalanine expansions in the spectrum of Müllerian fusion anomalies.

Jorgensen EM, Ruman JI, Doherty L, Taylor HS. Jorgensen EM, et al. Fertil Steril. 2010 Sep;94(4):1235-1238. doi: 10.1016/j.fertnstert.2009.05.057. Epub 2009 Jul 9. Fertil Steril. 2010. PMID: 19591980 Free PMC article.

10

Hallux valgus interphalangeus and a novel mutation in HOXA13. Part of the broadening spectrum of Hand-Foot-Genital syndrome.

Parker L, Mangwani J, Wakeling E, Singh D. Parker L, et al. Foot Ankle Surg. 2011 Jun;17(2):e28-30. doi: 10.1016/j.fas.2010.12.003. Epub 2011 Jan 19. Foot Ankle Surg. 2011. PMID: 21549968

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