Erickson RP - Search Results

1

Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.

Fang J, Dagenais SL, Erickson RP, Arlt MF, Glynn MW, Gorski JL, Seaver LH, Glover TW. Fang J, et al. Among authors: erickson rp. Am J Hum Genet. 2000 Dec;67(6):1382-8. doi: 10.1086/316915. Epub 2000 Nov 8. Am J Hum Genet. 2000. PMID: 11078474 Free PMC article.

2

FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome.

Kriederman BM, Myloyde TL, Witte MH, Dagenais SL, Witte CL, Rennels M, Bernas MJ, Lynch MT, Erickson RP, Caulder MS, Miura N, Jackson D, Brooks BP, Glover TW. Kriederman BM, et al. Among authors: erickson rp. Hum Mol Genet. 2003 May 15;12(10):1179-85. doi: 10.1093/hmg/ddg123. Hum Mol Genet. 2003. PMID: 12719382

3

Foxc2 is expressed in developing lymphatic vessels and other tissues associated with lymphedema-distichiasis syndrome.

Dagenais SL, Hartsough RL, Erickson RP, Witte MH, Butler MG, Glover TW. Dagenais SL, et al. Among authors: erickson rp. Gene Expr Patterns. 2004 Oct;4(6):611-9. doi: 10.1016/j.modgep.2004.07.004. Gene Expr Patterns. 2004. PMID: 15465483

4

Clinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations.

Erickson RP, Dagenais SL, Caulder MS, Downs CA, Herman G, Jones MC, Kerstjens-Frederikse WS, Lidral AC, McDonald M, Nelson CC, Witte M, Glover TW. Erickson RP, et al. J Med Genet. 2001 Nov;38(11):761-6. doi: 10.1136/jmg.38.11.761. J Med Genet. 2001. PMID: 11694548 Free PMC article.

5

Pulmonary atresia associated with maternal 22q11.2 deletion: possible parent of origin effect in the conotruncal anomaly face syndrome.

Seaver LH, Pierpont JW, Erickson RP, Donnerstein RL, Cassidy SB. Seaver LH, et al. Among authors: erickson rp. J Med Genet. 1994 Nov;31(11):830-4. doi: 10.1136/jmg.31.11.830. J Med Genet. 1994. PMID: 7853364 Free PMC article.

6

Female pseudohermaphroditism with multiple caudal anomalies: absence of Y-specific DNA sequences as pathogenetic factors.

Seaver LH, Grimes J, Erickson RP. Seaver LH, et al. Among authors: erickson rp. Am J Med Genet. 1994 May 15;51(1):16-21. doi: 10.1002/ajmg.1320510105. Am J Med Genet. 1994. PMID: 7913293

7

Bkm sequences from the human X chromosome contain large clusters of GATA/GACA repeats.

Erickson RP, Ross CE, Gorski JL, Stalvey JR, Drumm MM. Erickson RP, et al. Ann Hum Genet. 1988 Jul;52(3):167-76. doi: 10.1111/j.1469-1809.1988.tb01094.x. Ann Hum Genet. 1988. PMID: 3250328 Free article.

8

A "balanced" Y;16 translocation associated with Turner-like neonatal lymphedema suggests the location of a potential anti-Turner gene on the Y chromosome.

Erickson RP, Hudgins L, Stone JF, Schmidt S, Wilke C, Glover TW. Erickson RP, et al. Cytogenet Cell Genet. 1995;71(2):163-7. doi: 10.1159/000134099. Cytogenet Cell Genet. 1995. PMID: 7656589

9

Y;16 translocation breakpoint associated with a partial Turner phenotype identifies a foamy virus insertion.

Schmidt Drury S, Erickson RP, Glover TW. Schmidt Drury S, et al. Among authors: erickson rp. Cytogenet Cell Genet. 1998;80(1-4):199-203. doi: 10.1159/000014980. Cytogenet Cell Genet. 1998. PMID: 9678358

10

Polymerase chain reactions with alphoid-repeat primers in combination with Alu or LINEs primers, generate chromosome-specific DNA fragments.

Erickson RP, Glover TW, Hall BK, Witt M. Erickson RP, et al. Ann Hum Genet. 1991 Jul;55(3):199-211. doi: 10.1111/j.1469-1809.1991.tb00414.x. Ann Hum Genet. 1991. PMID: 1763884 Free article.

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