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Index « Auteurs » - entrée « R P Erickson »
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List of bibliographic references

Number of relevant bibliographic references: 12.
Ident.Authors (with country if any)Title
001378 (2014) R P EricksonNext generation sequencing is here now.
001698 (2014) R M Digiovanni ; R P Erickson ; E C Ohlson ; M. Bernas ; M H WitteA novel FLT4 mutation identified in a patient with Milroy disease.
001F36 (2012) R P EricksonMassively parallel DNA sequencing and the new approach to mutation detection: a step towards a lymphedema fine panel.
002B92 (2009) M H Witte [États-Unis] ; R P Erickson ; M. Khalil ; M. Dellinger ; M. Bernas ; T. Grogan ; H. Nitta ; J. Feng ; D. Duggan ; C L WitteLymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2.
002F08 (2008) M T Dellinger [États-Unis] ; K. Thome ; M J Bernas ; R P Erickson ; M H WitteNovel FOXC2 missense mutation identified in patient with lymphedema-distichiasis syndrome and review.
003662 (2006) A. Noon [États-Unis] ; R J Hunter ; M H Witte ; B. Kriederman ; M. Bernas ; M. Rennels ; D. Percy ; S. Enerb Ck ; R P EricksonComparative lymphatic, ocular, and metabolic phenotypes of Foxc2 haploinsufficient and aP2-FOXC2 transgenic mice.
004181 (2001) C J Holberg [États-Unis] ; R P Erickson ; M J Bernas ; M H Witte ; K E Fultz ; M. Andrade ; C L WitteSegregation analyses and a genome-wide linkage search confirm genetic heterogeneity and suggest oligogenic inheritance in some Milroy congenital primary lymphedema families.
004228 (2001) R P EricksonLymphedema-distichiasis and FOXC2 gene mutations.
004267 (2001) R P Erickson [États-Unis]Forkhead genes and human disease.
004297 (2001) R P Erickson [États-Unis] ; S L Dagenais ; M S Caulder ; C A Downs ; G. Herman ; M C Jones ; W S Kerstjens-Frederikse ; A C Lidral ; M. Mcdonald ; C C Nelson ; M. Witte ; T W GloverClinical heterogeneity in lymphoedema-distichiasis with FOXC2 truncating mutations.
004410 (2000) J. Fang [États-Unis] ; S L Dagenais ; R P Erickson ; M F Arlt ; M W Glynn ; J L Gorski ; L H Seaver ; T W GloverMutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndrome.
004D60 (1995) R P Erickson [États-Unis] ; L. Hudgins ; J F Stone ; S. Schmidt ; C. Wilke ; T W GloverA "balanced" Y;16 translocation associated with Turner-like neonatal lymphedema suggests the location of a potential anti-Turner gene on the Y chromosome.

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