These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

168 related articles for article (PubMed ID: 2064580)

  • 21. Distichiasis-lymphoedema syndrome: a family report.
    Temple IK; Collin JR
    Clin Dysmorphol; 1994 Apr; 3(2):139-42. PubMed ID: 8055133
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A Chinese pedigree of lymphoedema-distichiasis syndrome with a novel mutation in the FOXC2 gene.
    Zhu LL; Lv YN; Chen HD; Gao XH
    Clin Exp Dermatol; 2014 Aug; 39(6):731-3. PubMed ID: 24984567
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Hereditary late-onset lymphedema.
    Holmes LB; Fields JP; Zabriskie JB
    Pediatrics; 1978 Apr; 61(4):575-9. PubMed ID: 662482
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Lymphedema-distichiasis syndrome and FOXC2 gene mutation.
    Traboulsi EI; Al-Khayer K; Matsumoto M; Kimak MA; Crowe S; Wilson SE; Finegold DN; Ferrell RE; Meisler DM
    Am J Ophthalmol; 2002 Oct; 134(4):592-6. PubMed ID: 12383817
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Microdeletion of 16q24.1-q24.2-A unique etiology of Lymphedema-Distichiasis syndrome and neurodevelopmental disorder.
    Michelson M; Lidzbarsky G; Nishri D; Israel-Elgali I; Berger R; Gafner M; Shomron N; Lev D; Goldberg Y
    Am J Med Genet A; 2022 Jul; 188(7):1990-1996. PubMed ID: 35312147
    [TBL] [Abstract][Full Text] [Related]  

  • 26. A novel missense mutation and two microrearrangements in the FOXC2 gene of three families with lymphedema-distichiasis syndrome.
    Fauret AL; Tuleja E; Jeunemaitre X; Vignes S
    Lymphology; 2010 Mar; 43(1):14-8. PubMed ID: 20552815
    [TBL] [Abstract][Full Text] [Related]  

  • 27. c. 595-596 insC of FOXC2 underlies lymphedema, distichiasis, ptosis, ankyloglossia, and Robin sequence in a Thai patient.
    Tanpaiboon P; Kantaputra P; Wejathikul K; Piyamongkol W
    Am J Med Genet A; 2010 Mar; 152A(3):737-40. PubMed ID: 20186799
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Distichiasis-lymphedema syndrome and the Turner phenotype.
    Toro-Solá MA
    Bol Asoc Med P R; 1991 Dec; 83(12):543-4. PubMed ID: 1811607
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Distichiasis without lymphoedema?
    Patil BB; Bell R; Brice G; Jeffery S; Desai SP
    Eye (Lond); 2004 Dec; 18(12):1270-2. PubMed ID: 15044942
    [No Abstract]   [Full Text] [Related]  

  • 30. Lymphedema-distichiasis syndrome without FOXC2 mutation: evidence for chromosome 16 duplication upstream of FOXC2.
    Witte MH; Erickson RP; Khalil M; Dellinger M; Bernas M; Grogan T; Nitta H; Feng J; Duggan D; Witte CL
    Lymphology; 2009 Dec; 42(4):152-60. PubMed ID: 20218083
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24.
    Brice G; Mansour S; Bell R; Collin JR; Child AH; Brady AF; Sarfarazi M; Burnand KG; Jeffery S; Mortimer P; Murday VA
    J Med Genet; 2002 Jul; 39(7):478-83. PubMed ID: 12114478
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Microcephaly, intellectual impairment, bilateral vesicoureteral reflux, distichiasis, and glomuvenous malformations associated with a 16q24.3 contiguous gene deletion and a Glomulin mutation.
    Butler MG; Dagenais SL; Garcia-Perez JL; Brouillard P; Vikkula M; Strouse P; Innis JW; Glover TW
    Am J Med Genet A; 2012 Apr; 158A(4):839-49. PubMed ID: 22407726
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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
    Hum Mol Genet; 2003 May; 12(10):1179-85. PubMed ID: 12719382
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Distichiasis-lymphedema syndrome: tetralogy of Fallot, chylothorax, and neonatal death.
    Chen E; Larabell SK; Daniels JM; Goldstein S
    Am J Med Genet; 1996 Dec; 66(3):273-5. PubMed ID: 8985486
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Renal anomalies and lymphedema distichiasis syndrome. A rare association?
    Jones GE; Richmond AK; Navti O; Mousa HA; Abbs S; Thompson E; Mansour S; Vasudevan PC
    Am J Med Genet A; 2017 Aug; 173(8):2251-2256. PubMed ID: 28544699
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel complex insertion-deletion mutation in the FOXC2 gene in a Japanese patient with lymphedema-distichiasis syndrome.
    Itoh M; Nakagawa H
    Eur J Dermatol; 2013; 23(3):411-3. PubMed ID: 23747797
    [No Abstract]   [Full Text] [Related]  

  • 37. Clinicopathological case 2: lymphoedema-distichiasis syndrome.
    Ameen M; Brice G; Mortimer PS
    Clin Exp Dermatol; 2003 Jul; 28(4):463-4. PubMed ID: 12823324
    [No Abstract]   [Full Text] [Related]  

  • 38. FOXC2 truncating mutation in distichiasis, lymphedema, and cleft palate.
    Bahuau M; Houdayer C; Tredano M; Soupre V; Couderc R; Vazquez MP
    Clin Genet; 2002 Dec; 62(6):470-3. PubMed ID: 12485195
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Different lymphscintigraphic patterns in patients with lymphedema distichiasis.
    Sutkowska E; Bator A; Trompeta K; Szuba A
    Lymphology; 2010 Jun; 43(2):73-7. PubMed ID: 20848994
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Distichiasis of the lids and lymphedema of the lower extremities: a report of ten cases.
    Shammas HJ; Tabbara KF; Der Kaloustian VM
    J Pediatr Ophthalmol Strabismus; 1979; 16(2):129-32. PubMed ID: 458519
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 9.