PubMed for id: 355748

Year	Number of Results
1984	1
1996	1
1997	3
1998	1
1999	1
2001	1
2003	1
2004	1
2011	1
2013	1
2014	1
2015	2
2016	1
2019	2
2020	3
2021	3
2022	190
2023	259
2024	84

1

Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.

Lenassi E, Clayton-Smith J, Douzgou S, Ramsden SC, Ingram S, Hall G, Hardcastle CL, Fletcher TA, Taylor RL, Ellingford JM, Newman WD, Fenerty C, Sharma V, Lloyd IC, Biswas S, Ashworth JL, Black GC, Sergouniotis PI. Lenassi E, et al. Genet Med. 2020 Apr;22(4):745-751. doi: 10.1038/s41436-019-0722-8. Epub 2019 Dec 18. Genet Med. 2020. PMID: 31848469 Free PMC article.

2

Axenfeld-Rieger anomaly: a novel mutation in the forkhead box C1 (FOXC1) gene in a 4-generation family.

Mortemousque B, Amati-Bonneau P, Couture F, Graffan R, Dubois S, Colin J, Bonneau D, Morissette J, Lacombe D, Raymond V. Mortemousque B, et al. Arch Ophthalmol. 2004 Oct;122(10):1527-33. doi: 10.1001/archopht.122.10.1527. Arch Ophthalmol. 2004. PMID: 15477465

3

An interstitial deletion of 6p24-p25 proximal to the FKHL7 locus and including AP-2alpha that affects anterior eye chamber development.

Davies AF, Mirza G, Flinter F, Ragoussis J. Davies AF, et al. J Med Genet. 1999 Sep;36(9):708-10. J Med Genet. 1999. PMID: 10507730 Free PMC article.

4

Mutations of the forkhead/winged-helix gene, FKHL7, in patients with Axenfeld-Rieger anomaly.

Mears AJ, Jordan T, Mirzayans F, Dubois S, Kume T, Parlee M, Ritch R, Koop B, Kuo WL, Collins C, Marshall J, Gould DB, Pearce W, Carlsson P, Enerbäck S, Morissette J, Bhattacharya S, Hogan B, Raymond V, Walter MA. Mears AJ, et al. Am J Hum Genet. 1998 Nov;63(5):1316-28. doi: 10.1086/302109. Am J Hum Genet. 1998. PMID: 9792859 Free PMC article.

5

Fine mapping of the gene for autosomal dominant juvenile-onset glaucoma with iridogoniodysgenesis in 6p25-tel.

Graff C, Jerndal T, Wadelius C. Graff C, et al. Hum Genet. 1997 Dec;101(2):130-4. doi: 10.1007/s004390050601. Hum Genet. 1997. PMID: 9402956

6

CD19-regulated signaling thresholds control peripheral tolerance and autoantibody production in B lymphocytes.

Inaoki M, Sato S, Weintraub BC, Goodnow CC, Tedder TF. Inaoki M, et al. J Exp Med. 1997 Dec 1;186(11):1923-31. doi: 10.1084/jem.186.11.1923. J Exp Med. 1997. PMID: 9382890 Free PMC article.

7

Identification of the human chromosomal region containing the iridogoniodysgenesis anomaly locus by genomic-mismatch scanning.

Mirzayans F, Mears AJ, Guo SW, Pearce WG, Walter MA. Mirzayans F, et al. Am J Hum Genet. 1997 Jul;61(1):111-9. doi: 10.1086/513894. Am J Hum Genet. 1997. PMID: 9245991 Free PMC article.

8

Autosomal dominant iridogoniodysgenesis anomaly maps to 6p25.

Mears AJ, Mirzayans F, Gould DB, Pearce WG, Walter MA. Mears AJ, et al. Am J Hum Genet. 1996 Dec;59(6):1321-7. Am J Hum Genet. 1996. PMID: 8940278 Free PMC article.

9

Allotypic specificities of murine IgD and IgM recognized by monoclonal antibodies.

Stall AM, Loken MR. Stall AM, et al. J Immunol. 1984 Feb;132(2):787-95. J Immunol. 1984. PMID: 6690619

10

Detecting and phasing minor single-nucleotide variants from long-read sequencing data.

Feng Z, Clemente JC, Wong B, Schadt EE. Feng Z, et al. Nat Commun. 2021 May 24;12(1):3032. doi: 10.1038/s41467-021-23289-4. Nat Commun. 2021. PMID: 34031367 Free PMC article.

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