Similar articles for PMID: 29610615

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1

Surgical Management of Facial Features of Robinow Syndrome: A Case Report.

Mossaad AM, Abdelrahman MA, Ibrahim MA, Al Ahmady HH. Mossaad AM, et al. Open Access Maced J Med Sci. 2018 Mar 10;6(3):536-539. doi: 10.3889/oamjms.2018.129. eCollection 2018 Mar 15. Open Access Maced J Med Sci. 2018. PMID: 29610615 Free PMC article.

2

ROR2-Related Robinow Syndrome.

Bacino CA. Bacino CA. 2005 Jul 28 [updated 2019 Sep 12]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2005 Jul 28 [updated 2019 Sep 12]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301418 Free Books & Documents. Review.

3

Robinow Syndrome: A Rare Case Report and Review of Literature.

Soman C, Lingappa A. Soman C, et al. Int J Clin Pediatr Dent. 2015 May-Aug;8(2):149-52. doi: 10.5005/jp-journals-10005-1303. Epub 2015 Aug 11. Int J Clin Pediatr Dent. 2015. PMID: 26379386 Free PMC article.

4

Dental management and orofacial manifestations of a patient with Robinow Syndrome.

Basman A, Akay G, Peker I, Gungor K, Akarslan Z, Ozcan S, Ucok CO. Basman A, et al. J Istanb Univ Fac Dent. 2017 Apr 3;51(2):43-48. doi: 10.17096/jiufd.86251. eCollection 2017. J Istanb Univ Fac Dent. 2017. PMID: 28955595 Free PMC article.

5

Identification of novel ROR2 gene mutations in Indian children with Robinow syndrome.

Tamhankar PM, Vasudevan L, Kondurkar S, Yashaswini K, Agarwalla SK, Nair M, Ramkumar TV, Chaubal N, Chennuri VS. Tamhankar PM, et al. J Clin Res Pediatr Endocrinol. 2014;6(2):79-83. doi: 10.4274/Jcrpe.1233. J Clin Res Pediatr Endocrinol. 2014. PMID: 24932600 Free PMC article.

6

A case report on autosomal recessive Robinow syndrome.

Eronat N, Cogulu D, Ozkinay F. Eronat N, et al. Eur J Paediatr Dent. 2009 Sep;10(3):147-50. Eur J Paediatr Dent. 2009. PMID: 19761290

7

Robinow Syndrome: A Rare Diagnosis.

Mishra S, Agarwalla SK, Pradhan S. Mishra S, et al. J Clin Diagn Res. 2015 Dec;9(12):SD04-5. doi: 10.7860/JCDR/2015/15078.6949. Epub 2015 Dec 1. J Clin Diagn Res. 2015. PMID: 26816964 Free PMC article.

8

Autosomal recessive Robinow syndrome: a case report.

Grothe R, Anderson-Cermin C, Beiraghi S. Grothe R, et al. J Dent Child (Chic). 2008 Jan-Apr;75(1):48-54. J Dent Child (Chic). 2008. PMID: 18505648

9

[Robinow's syndrome associated with deafness].

Samoud A, Menif K, Boulaares M, Ben Dridi MF. Samoud A, et al. Arch Fr Pediatr. 1993 Dec;50(10):897-9. Arch Fr Pediatr. 1993. PMID: 8053771 French.

10

One gene, two phenotypes: ROR2 mutations in autosomal recessive Robinow syndrome and autosomal dominant brachydactyly type B.

Afzal AR, Jeffery S. Afzal AR, et al. Hum Mutat. 2003 Jul;22(1):1-11. doi: 10.1002/humu.10233. Hum Mutat. 2003. PMID: 12815588

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