Similar articles for PMID: 11897823

Year	Number of Results
1993	4
1994	3
1995	11
1996	12
1997	8
1998	10
1999	11
2000	11
2001	5
2002	7
2003	9
2004	5
2005	5
2008	1
2009	3
2011	2
2012	1
2017	1
2018	2
2019	1
2024	0

1

A single base alteration in the CGG repeat region of FMR1: possible effects on gene expression and phenotype.

Tarleton J, Kenneson A, Taylor AK, Crandall K, Fletcher R, Casey R, Hart PS, Hatton D, Fisch G, Warren ST. Tarleton J, et al. J Med Genet. 2002 Mar;39(3):196-200. doi: 10.1136/jmg.39.3.196. J Med Genet. 2002. PMID: 11897823 Free PMC article. No abstract available.

2

Mosaicism for the fragile X syndrome full mutation and deletions within the CGG repeat of the FMR1 gene.

Milà M, Castellví-Bel S, Sánchez A, Lázaro C, Villa M, Estivill X. Milà M, et al. J Med Genet. 1996 Apr;33(4):338-40. doi: 10.1136/jmg.33.4.338. J Med Genet. 1996. PMID: 8730293 Free PMC article.

3

Distribution of CGG repeat sizes within the fragile X mental retardation 1 (FMR1) homologue in a non-human primate population.

Garcia Arocena D, Breece KE, Hagerman PJ. Garcia Arocena D, et al. Hum Genet. 2003 Oct;113(5):371-6. doi: 10.1007/s00439-003-0982-9. Epub 2003 Aug 7. Hum Genet. 2003. PMID: 12905066

4

Normal phenotype in two brothers with a full FMR1 mutation.

Smeets HJ, Smits AP, Verheij CE, Theelen JP, Willemsen R, van de Burgt I, Hoogeveen AT, Oosterwijk JC, Oostra BA. Smeets HJ, et al. Hum Mol Genet. 1995 Nov;4(11):2103-8. doi: 10.1093/hmg/4.11.2103. Hum Mol Genet. 1995. PMID: 8589687

5

Mosaicism for FMR1 and FMR2 deletion: a new case.

Fengler S, Fuchs S, König R, Arnemann J. Fengler S, et al. J Med Genet. 2002 Mar;39(3):200-1. doi: 10.1136/jmg.39.3.200. J Med Genet. 2002. PMID: 11897824 Free PMC article. No abstract available.

6

Mosaicism in a fragile X male including a de novo deletion in the FMR1 gene.

Petek E, Kroisel PM, Schuster M, Zierler H, Wagner K. Petek E, et al. Am J Med Genet. 1999 May 28;84(3):229-32. Am J Med Genet. 1999. PMID: 10331598

7

Mosaicism for the full mutation and a microdeletion involving the CGG repeat and flanking sequences in the FMR1 gene in eight fragile X patients.

Grasso M, Faravelli F, Lo Nigro C, Chiurazzi P, Sperandeo MP, Argusti A, Pomponi MG, Lecora M, Sebastio GF, Perroni L, Andria G, Neri G, Bricarelli FD. Grasso M, et al. Am J Med Genet. 1999 Jul 30;85(3):311-6. doi: 10.1002/(sici)1096-8628(19990730)85:3<311::aid-ajmg24>3.0.co;2-a. Am J Med Genet. 1999. PMID: 10398249

8

Apparently unstable normal FMR1 alleles in nine developmentally delayed patients: implications for molecular diagnosis of the fragile X syndrome.

Tzountzouris J, Kennedy D, Skuterud M, Connolly-Wilson M, Holden JJ, Lin CC, Mak-Tam E, Somerville MJ, Summers AM, Allingham-Hawkins DJ. Tzountzouris J, et al. Genet Test. 2000;4(3):235-9. doi: 10.1089/10906570050501434. Genet Test. 2000. PMID: 11142752

9

Frequencies of "grey-zone" and premutation-size FMR1 CGG-repeat alleles in patients with developmental disability in Cyprus and Canada.

Patsalis PC, Sismani C, Hettinger JA, Holden JJ, Lawson JS, Chalifoux M, Wing M, Walker M, Leggo J. Patsalis PC, et al. Am J Med Genet. 1999 May 28;84(3):195-7. Am J Med Genet. 1999. PMID: 10331589 No abstract available.

10

A methylation PCR approach for detection of fragile X syndrome.

Panagopoulos I, Lassen C, Kristoffersson U, Aman P. Panagopoulos I, et al. Hum Mutat. 1999;14(1):71-9. doi: 10.1002/(SICI)1098-1004(1999)14:1<71::AID-HUMU9>3.0.CO;2-5. Hum Mutat. 1999. PMID: 10447261

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