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1993 1
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Page 1
TEK-Related Venous Malformations.
Seront E, Boon LM, Vikkula M. Seront E, et al. 2008 Sep 18 [updated 2023 Mar 2]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2008 Sep 18 [updated 2023 Mar 2]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 20301733 Free Books & Documents. Review.
Contemporary management of vascular malformations.
Colletti G, Valassina D, Bertossi D, Melchiorre F, Vercellio G, Brusati R. Colletti G, et al. J Oral Maxillofac Surg. 2014 Mar;72(3):510-28. doi: 10.1016/j.joms.2013.08.008. Epub 2013 Oct 16. J Oral Maxillofac Surg. 2014. PMID: 24139296 Review.
Glomuvenous malformations.
Henning JS, Kovich OI, Schaffer JV. Henning JS, et al. Dermatol Online J. 2007 Jan 27;13(1):17. Dermatol Online J. 2007. PMID: 17511950 Free article.
This autosomal dominant condition, which is due to mutations in the GLMN gene, presents with clinical findings that are distinct from those of familial, multiple, cutaneous and mucosal venous malformations. Treatment options include excis …
This autosomal dominant condition, which is due to mutations in the GLMN gene, presents with clinical findings that are distinct from those …
Update on the molecular genetics of vascular anomalies.
Wang QK. Wang QK. Lymphat Res Biol. 2005;3(4):226-33. doi: 10.1089/lrb.2005.3.226. Lymphat Res Biol. 2005. PMID: 16379592 Free PMC article. Review.
These genes include AGGF1 for Klippel-Trenaunay syndrome, RASA1 for capillary malformations, KRIT1, MGC4607, PDCD10 for cerebral cavernous malformations, glomulin for glomuvenous malformations, TIE2 for multiple cutaneous and mucosal venous m
These genes include AGGF1 for Klippel-Trenaunay syndrome, RASA1 for capillary malformations, KRIT1, MGC4607, PDCD10 for cerebral cavernous m …
Assignment of a locus for dominantly inherited venous malformations to chromosome 9p.
Boon LM, Mulliken JB, Vikkula M, Watkins H, Seidman J, Olsen BR, Warman ML. Boon LM, et al. Hum Mol Genet. 1994 Sep;3(9):1583-7. doi: 10.1093/hmg/3.9.1583. Hum Mol Genet. 1994. PMID: 7833915
We have mapped the locus for an autosomal dominant disorder in a three generation family that manifests as multiple cutaneous and mucosal venous malformations. This locus lies within a 24 cM interval on chromosome 9p, defined by the marke …
We have mapped the locus for an autosomal dominant disorder in a three generation family that manifests as multiple cutaneous
Hereditary haemorrhagic telangiectasia with extensive liver involvement is not caused by either HHT1 or HHT2.
Piantanida M, Buscarini E, Dellavecchia C, Minelli A, Rossi A, Buscarini L, Danesino C. Piantanida M, et al. J Med Genet. 1996 Jun;33(6):441-3. doi: 10.1136/jmg.33.6.441. J Med Genet. 1996. PMID: 8782041 Free PMC article.
The loci for two other inherited vascular malformation diseases, cerebral cavernous malformations and multiple cutaneous and mucosal venous malformations, have also been excluded. ...
The loci for two other inherited vascular malformation diseases, cerebral cavernous malformations and multiple cutaneous an
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