Best matches for Fragile x syndrome AND (genetic OR genomic) AND review:
Fragile X syndrome.Saldarriaga W et al. Colomb Med (Cali). (2014)
Public Health Literature Review of Fragile X Syndrome.Raspa M et al. Pediatrics. (2017)
FMR1 CGG repeat expansion mutation detection and linked haplotype analysis for reliable and accurate preimplantation genetic diagnosis of fragile X syndrome.Rajan-Babu IS et al. Expert Rev Mol Med. (2017)
1.
Bartholomay KL, Lee CH, Bruno JL, Lightbody AA, Reiss AL.
Brain Sci. 2019 Jan 12;9(1). pii: E11. doi: 10.3390/brainsci9010011. Review.
2.
Fink DA, Nelson LM, Pyeritz R, Johnson J, Sherman SL, Cohen Y, Elizur SE.
Front Genet. 2018 Nov 27;9:529. doi: 10.3389/fgene.2018.00529. eCollection 2018. Review.
3.
Rais M, Binder DK, Razak KA, Ethell IM.
ASN Neuro. 2018 Jan-Dec;10:1759091418801092. doi: 10.1177/1759091418801092.
4.
Gabis LV, Shefer S, Gruber N, Raviv R, Cohen Y, Berkenstadt M, Ries-Levavi L, Pinhas-Hamiel O, Elizur S.
Harefuah. 2018 Aug;157(8):529-533. Review. Hebrew.
- PMID:
- 30175572
5.
Wen TH, Binder DK, Ethell IM, Razak KA.
Front Mol Neurosci. 2018 Aug 3;11:270. doi: 10.3389/fnmol.2018.00270. eCollection 2018. Review.
6.
Kraan CM, Godler DE, Amor DJ.
Dev Med Child Neurol. 2018 Aug 7. doi: 10.1111/dmcn.13985. [Epub ahead of print] Review.
- PMID:
- 30084485
7.
Rudich P, Lamitina T.
J Genet. 2018 Jul;97(3):665-677. Review.
8.
Nakai N, Takumi T, Nakai J, Sato M.
Front Neurosci. 2018 Jun 19;12:412. doi: 10.3389/fnins.2018.00412. eCollection 2018. Review.
9.
Kanani F, Study D, Balasubramanian M.
Clin Dysmorphol. 2018 Oct;27(4):113-115. doi: 10.1097/MCD.0000000000000232. Review.
- PMID:
- 29939863
10.
Serrano M.
Handb Clin Neurol. 2018;155:227-244. doi: 10.1016/B978-0-444-64189-2.00015-9. Review.
- PMID:
- 29891061
11.
Faundez V, De Toma I, Bardoni B, Bartesaghi R, Nizetic D, de la Torre R, Cohen Kadosh R, Herault Y, Dierssen M, Potier MC; Down Syndrome and Other Genetic Developmental Disorders ECNP Network.
Eur Neuropsychopharmacol. 2018 Jun;28(6):675-690. doi: 10.1016/j.euroneuro.2018.03.006. Epub 2018 Jun 7. Review.
- PMID:
- 29887288
12.
Dockendorff TC, Labrador M.
Mol Neurobiol. 2019 Jan;56(1):711-721. doi: 10.1007/s12035-018-1122-9. Epub 2018 May 23. Review.
- PMID:
- 29796988
13.
Drozd M, Bardoni B, Capovilla M.
Front Mol Neurosci. 2018 Apr 16;11:124. doi: 10.3389/fnmol.2018.00124. eCollection 2018. Review.
14.
Elizur S, Berkenstadt M, Ries-Levavi L, Gruber N, Pinhas-Hamiel O, Hassin-Baer S, Raas-Rothschild A, Raanani H, Cukierman-Yaffe T, Orvieto R, Cohen Y, Gabis L.
Harefuah. 2018 Apr;157(4):241-244. Review. Hebrew.
- PMID:
- 29688643
15.
Lubala TK, Lumaka A, Kanteng G, Mutesa L, Mukuku O, Wembonyama S, Hagerman R, Luboya ON, Lukusa Tshilobo P.
Mol Genet Genomic Med. 2018 Apr 6. doi: 10.1002/mgg3.398. [Epub ahead of print]
16.
Deffrennes C, De Clercq M, Vallée L, Lemaître MP.
Arch Pediatr. 2018 Apr;25(3):223-228. doi: 10.1016/j.arcped.2018.01.001. Epub 2018 Mar 14. Review. French.
- PMID:
- 29549980
17.
Hardiman RL, McGill P.
Res Dev Disabil. 2018 May;76:99-109. doi: 10.1016/j.ridd.2018.02.020. Epub 2018 Mar 7. Review.
- PMID:
- 29525058
18.
Li EH, Zhao X, Zhang C, Liu W.
Yi Chuan. 2018 Feb 20;40(2):87-94. doi: 10.16288/j.yczz.17-255. Review.
- PMID:
- 29428901
19.
Fernandez BA, Scherer SW.
Dialogues Clin Neurosci. 2017 Dec;19(4):353-371. Review.
20.
Hannan AJ.
Nat Rev Genet. 2018 May;19(5):286-298. doi: 10.1038/nrg.2017.115. Epub 2018 Feb 5. Review.
- PMID:
- 29398703
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