List of bibliographic references indexed by Cils
Number of relevant bibliographic references: 69.
[20-40] [
0 - 20][
0 - 50][
40-60]
| Ident. | Authors (with country if any) | Title |
|---|
| 005B38 (2010) |
Pranoot Tanpaiboon [Thaïlande] ; Piranit Kantaputra [Thaïlande] ; Karn Wejathikul [Thaïlande] ; Wirawit Piyamongkol [Thaïlande] | c. 595‐596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient |
| 006182 (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 Witte | Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2. |
| 006A01 (2008) |
M T Dellinger [États-Unis] ; K. Thome ; M J Bernas ; R P Erickson ; M H Witte | Novel FOXC2 missense mutation identified in patient with lymphedema-distichiasis syndrome and review. |
| 006D68 (2008) |
Fiona Connell ; Glen Brice ; Peter Mortimer (dermatologue) [Royaume-Uni] | Phenotypic Characterization of Primary Lymphedema |
| 006D71 (2008) |
Glen Brice [Royaume-Uni] | Perinatal diagnosis of a lymphoedema‐distichiasis syndrome |
| 006E09 (2008) |
Maaike Vreeburg ; Martijn V. Heitink ; Robert J. Damstra [Allemagne] ; Ute Moog [Allemagne] ; Michel Van Geel [Allemagne] ; Maurice A. M. Van Steensel [Allemagne] | Lymphedema–distichiasis syndrome: a distinct type of primary lymphedema caused by mutations in the FOXC2 gene |
| 007365 (2007) |
Zeynep Celebi Sözener [Turquie] ; Mustafa Tekin ; Dil Ad Mungan ; Demet Karnak | A 15-year-old girl with swelling of the face, legs, breast, and eyes. |
| 007686 (2007) |
S. Kumar [Arabie saoudite] ; C. Carver ; S. Mccall ; G. Brice ; P. Ostergaard ; Peter Mortimer (dermatologue) [Royaume-Uni] ; S. Jeffery [Royaume-Uni] | A family with lymphoedema‐distichiasis where identical twins have a discordant phenotype |
| 007A17 (2006) |
A. Noon [États-Unis] ; R J Hunter ; M H Witte ; B. Kriederman ; M. Bernas ; M. Rennels ; D. Percy ; S. Enerb Ck ; R P Erickson | Comparative lymphatic, ocular, and metabolic phenotypes of Foxc2 haploinsufficient and aP2-FOXC2 transgenic mice. |
| 007E27 (2005) |
C. Guerrero Laleona ; S. Gimeno Aguilar ; D. Portilla C Rdova ; A. Honrrubia Grijalbo | [Distichiasis-lymphedema syndrome]. |
| 008103 (2005) |
Fred B. Berry ; Yahya Tamimi [Canada] ; Michelle V. Carle ; Ordan J. Lehmann [Canada] ; Michael A. Walter [Canada] | The establishment of a predictive mutational model of the forkhead domain through the analyses of FOXC2 missense mutations identified in patients with hereditary lymphedema with distichiasis |
| 008822 (2004) |
B B Patil ; R. Bell ; G. Brice ; S. Jeffery ; S P Desai | Distichiasis without lymphoedema? |
| 008E38 (2003) |
Brian P. Brooks [États-Unis] ; Susan L. Dagenais ; Christine C. Nelson ; Michael W. Glynn ; Mark S. Caulder ; Catherine A. Downs ; Thomas W. Glover | Mutation of the FOXC2 gene in familial distichiasis. |
| 008F22 (2003) |
M. Ameen [Royaume-Uni] ; G. Brice ; Peter Mortimer (dermatologue) [Royaume-Uni] | Clinicopathological case 2: lymphoedema-distichiasis syndrome. |
| 009136 (2003) |
Benjamin M. Kriederman ; Teressa L. Myloyde ; Marlys H. Witte ; Susan L. Dagenais ; Charles L. Witte ; Margaret Rennels ; Michael J. Bernas ; Michelle T. Lynch ; Robert P. Erickson ; Mark S. Caulder ; Naoyuki Miura ; David Jackson [Royaume-Uni] ; Brian P. Brooks [États-Unis] ; Thomas W. Glover | FOXC2 haploinsufficient mice are a model for human autosomal dominant lymphedema-distichiasis syndrome |
| 009609 (2002) |
Imad R. Makhoul [Israël] ; Polo Sujov [Israël] ; Nadir Ghanem [Israël] ; Moshe Bronshtein [Israël] | Prenatal diagnosis of Milroy's primary congenital lymphedema |
| 009702 (2002) |
S. Jeffery [Royaume-Uni] | How double eyelashes give you swollen legs |
| 009721 (2002) |
M. Bahuau [France] ; C. Houdayer ; M. Tredano ; V. Soupre [France] ; R. Couderc ; M-P Vazquez [France] | FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate |
| 009791 (2002) |
G. Brice [Royaume-Uni] ; S. Mansour [Royaume-Uni] ; R. Bell [Royaume-Uni] ; J R O. Collin [Royaume-Uni] ; A H Child [Royaume-Uni] ; A F Brady [Royaume-Uni] ; M. Sarfarazi [États-Unis] ; K G Burnand [Royaume-Uni] ; S. Jeffery [Royaume-Uni] ; Peter Mortimer (dermatologue) [Royaume-Uni] ; V A Murday [Royaume-Uni] | Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24 |
| 009889 (2002) |
Elias I. Traboulsi [États-Unis] ; Khouloud Al-Khayer [États-Unis] ; Masayuki Matsumoto [États-Unis] ; Mark A. Kimak [États-Unis] ; Susan Crowe [États-Unis] ; Steven E. Wilson [États-Unis] ; David N. Finegold [États-Unis] ; Robert E. Ferrell [États-Unis] ; David M. Meisler [États-Unis] | Lymphedema-distichiasis syndrome and FOXC2 gene mutation |
| 009E36 (2001) |
Marika J. Karkkainen [Finlande] ; Lotta Jussila [Finlande] ; Kari Alitalo [Finlande] ; Robert E. Ferrell ; David N. Finegold | Molecular regulation of lymphangiogenesis and targets for tissue oedema |
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