Similar articles for PMID: 24357154

Year	Number of Results
1983	1
1985	1
1988	1
1989	2
1990	1
1991	1
1993	3
1994	5
1995	4
1996	1
1998	1
2000	4
2002	5
2003	2
2004	6
2005	5
2006	5
2007	5
2008	7
2009	4
2010	5
2011	5
2012	6
2013	8
2014	13
2015	7
2016	10
2017	9
2018	8
2019	4
2020	13
2021	9
2022	10
2023	3
2024	0

1

Fryns syndrome without diaphragmatic hernia, DOOR syndrome or Fryns-like syndrome? Report on patients from Indian Ocean islands.

Alessandri JL, Cuillier F, Malan V, Brayer C, Grondard M, Jacquemot-Dekkak L, Kieffer-Traversier M, Pierre F, Laurain C, Samperiz S, Tiran-Rajaofera I, Ramful D. Alessandri JL, et al. Am J Med Genet A. 2014 Mar;164A(3):648-54. doi: 10.1002/ajmg.a.36323. Epub 2013 Dec 19. Am J Med Genet A. 2014. PMID: 24357154

2

Fryns syndrome: a case associated with karyotype XO.

Dawani NM, Al Madhoob AR, Ali FA, Shabib F. Dawani NM, et al. Ann Saudi Med. 2004 Mar-Apr;24(2):129-32. doi: 10.5144/0256-4947.2004.129. Ann Saudi Med. 2004. PMID: 15323276 Free PMC article. No abstract available.

3

[Fryns syndrome. Report on 3 new cases].

Alessandri JL, Attali T, Brayer C, Dupuy L, Pilorget H, Ramful D, Samperiz S, Tiran-Rajaofera I, Robin S. Alessandri JL, et al. Arch Pediatr. 2007 Jul;14(7):903-7. doi: 10.1016/j.arcped.2007.03.015. Epub 2007 Apr 17. Arch Pediatr. 2007. PMID: 17442547 French.

4

Congenital diaphragmatic hernia and early lethality in PIGL-related disorder.

Winter-Paquette LM, Al Suwaidi HH, Sajjad Y, Bricker L. Winter-Paquette LM, et al. Eur J Med Genet. 2022 May;65(5):104501. doi: 10.1016/j.ejmg.2022.104501. Epub 2022 Apr 1. Eur J Med Genet. 2022. PMID: 35378319

5

[Unusual facies with delayed development and multiple malformations in a 14-month-old boy].

Lu T, Wang Y. Lu T, et al. Zhongguo Dang Dai Er Ke Za Zhi. 2017 Aug;19(8):921-925. doi: 10.7499/j.issn.1008-8830.2017.08.014. Zhongguo Dang Dai Er Ke Za Zhi. 2017. PMID: 28774369 Free PMC article. Chinese.

6

Prenatal presentation of Mabry syndrome with congenital diaphragmatic hernia and phenotypic overlap with Fryns syndrome.

Reynolds KK, Juusola J, Rice GM, Giampietro PF. Reynolds KK, et al. Am J Med Genet A. 2017 Oct;173(10):2776-2781. doi: 10.1002/ajmg.a.38379. Epub 2017 Aug 17. Am J Med Genet A. 2017. PMID: 28817240

7

DOOR syndrome: A case report and its embryological basis.

Santos M, Reis-Rego Â, Coutinho M, Almeida E Sousa C. Santos M, et al. Int J Pediatr Otorhinolaryngol. 2019 Feb;117:57-60. doi: 10.1016/j.ijporl.2018.11.015. Epub 2018 Nov 14. Int J Pediatr Otorhinolaryngol. 2019. PMID: 30579089

8

Unusual neuroradiological features in Schinzel-Giedion syndrome: a novel case.

Lestner JM, Chong WK, Offiiah A, Kefas J, Vandersteen AM. Lestner JM, et al. Clin Dysmorphol. 2012 Jul;21(3):152-154. doi: 10.1097/MCD.0b013e3283518f1e. Clin Dysmorphol. 2012. PMID: 22473152 No abstract available.

9

Fryns syndrome: a surviving case with associated Hirschsprung's disease and hemidiaphragmatic agenesis.

Davis C, Samarakkody U. Davis C, et al. J Paediatr Child Health. 2002 Jun;38(3):318-20. doi: 10.1046/j.1440-1754.2002.00820.x. J Paediatr Child Health. 2002. PMID: 12047706

10

Findings from aCGH in patients with congenital diaphragmatic hernia (CDH): a possible locus for Fryns syndrome.

Kantarci S, Casavant D, Prada C, Russell M, Byrne J, Haug LW, Jennings R, Manning S, Boyd TK, Fryns JP, Holmes LB, Donahoe PK, Lee C, Kimonis V, Pober BR. Kantarci S, et al. Am J Med Genet A. 2006 Jan 1;140(1):17-23. doi: 10.1002/ajmg.a.31025. Am J Med Genet A. 2006. PMID: 16333846 Free PMC article.

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