PubMed (OMIM) for id: 341339

Year	Number of Results
1986	1
1992	1
1993	1
1994	1
1998	4
1999	1
2000	3
2002	1
2004	3
2005	1
2024	0

1

Mutations in FLNB cause boomerang dysplasia.

Bicknell LS, Morgan T, Bonafé L, Wessels MW, Bialer MG, Willems PJ, Cohn DH, Krakow D, Robertson SP. Bicknell LS, et al. J Med Genet. 2005 Jul;42(7):e43. doi: 10.1136/jmg.2004.029967. J Med Genet. 2005. PMID: 15994868 Free PMC article.

2

A locus for spondylocarpotarsal synostosis syndrome at chromosome 3p14.

Steiner C, Ehtesham N, Taylor KD, Sebald E, Cantor R, King LM, Guo X, Hang T, Hu MS, Cui JR, Friedman B, Norato D, Allanson J, Honeywell C, Mettler G, Field F, Lachman R, Cohn DH, Krakow D. Steiner C, et al. J Med Genet. 2004 Apr;41(4):266-9. doi: 10.1136/jmg.2003.012252. J Med Genet. 2004. PMID: 15060099 Free PMC article.

3

Phenotype matters.

Biesecker LG. Biesecker LG. Nat Genet. 2004 Apr;36(4):323-4. doi: 10.1038/ng0404-323. Nat Genet. 2004. PMID: 15054484 No abstract available.

4

Mutations in the gene encoding filamin B disrupt vertebral segmentation, joint formation and skeletogenesis.

Krakow D, Robertson SP, King LM, Morgan T, Sebald ET, Bertolotto C, Wachsmann-Hogiu S, Acuna D, Shapiro SS, Takafuta T, Aftimos S, Kim CA, Firth H, Steiner CE, Cormier-Daire V, Superti-Furga A, Bonafe L, Graham JM Jr, Grix A, Bacino CA, Allanson J, Bialer MG, Lachman RS, Rimoin DL, Cohn DH. Krakow D, et al. Nat Genet. 2004 Apr;36(4):405-10. doi: 10.1038/ng1319. Epub 2004 Feb 29. Nat Genet. 2004. PMID: 14991055

5

Filamin A and Filamin B are co-expressed within neurons during periods of neuronal migration and can physically interact.

Sheen VL, Feng Y, Graham D, Takafuta T, Shapiro SS, Walsh CA. Sheen VL, et al. Hum Mol Genet. 2002 Nov 1;11(23):2845-54. doi: 10.1093/hmg/11.23.2845. Hum Mol Genet. 2002. PMID: 12393796

6

Genomic structure and fine mapping of the two human filamin gene paralogues FLNB and FLNC and comparative analysis of the filamin gene family.

Chakarova C, Wehnert MS, Uhl K, Sakthivel S, Vosberg HP, van der Ven PF, Fürst DO. Chakarova C, et al. Hum Genet. 2000 Dec;107(6):597-611. doi: 10.1007/s004390000414. Hum Genet. 2000. PMID: 11153914

7

Spondylocarpotarsal synostosis syndrome and cervical instability.

Seaver LH, Boyd E. Seaver LH, et al. Am J Med Genet. 2000 Apr 24;91(5):340-4. doi: 10.1002/(sici)1096-8628(20000424)91:5<340::aid-ajmg3>3.0.co;2-n. Am J Med Genet. 2000. PMID: 10766994

8

Spondylocarpotarsal synostosis with ocular findings.

Steiner CE, Torriani M, Norato DY, Marques-de-Faria AP. Steiner CE, et al. Am J Med Genet. 2000 Mar 13;91(2):131-4. Am J Med Genet. 2000. PMID: 10748412

9

Assignment of human filamin gene FLNB to human chromosome band 3p14.3 and identification of YACs containing the complete FLNB transcribed region.

Bröcker F, Bardenheuer W, Vieten L, Jülicher K, Werner N, Marquitan G, Michael D, Opalka B, Schütte J. Bröcker F, et al. Cytogenet Cell Genet. 1999;85(3-4):267-8. doi: 10.1159/000015309. Cytogenet Cell Genet. 1999. PMID: 10449914 No abstract available.

10

A novel human actin-binding protein homologue that binds to platelet glycoprotein Ibalpha.

Xu Wf, Xie Z, Chung DW, Davie EW. Xu Wf, et al. Blood. 1998 Aug 15;92(4):1268-76. Blood. 1998. PMID: 9694715 Free article.

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