Sybert VP - Search Results

1

Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.

Wright JT, Fete M, Schneider H, Zinser M, Koster MI, Clarke AJ, Hadj-Rabia S, Tadini G, Pagnan N, Visinoni AF, Bergendal B, Abbott B, Fete T, Stanford C, Butcher C, D'Souza RN, Sybert VP, Morasso MI. Wright JT, et al. Among authors: sybert vp. Am J Med Genet A. 2019 Mar;179(3):442-447. doi: 10.1002/ajmg.a.61045. Epub 2019 Jan 31. Am J Med Genet A. 2019. PMID: 30703280 Free PMC article. Review.

2

International Research Symposium on Ankyloblepharon-Ectodermal Defects-Cleft Lip/Palate (AEC) syndrome.

Fete M, vanBokhoven H, Clements SE, McKeon F, Roop DR, Koster MI, Missero C, Attardi LD, Lombillo VA, Ratovitski E, Julapalli M, Ruths D, Sybert VP, Siegfried EC, Bree AF. Fete M, et al. Among authors: sybert vp. Am J Med Genet A. 2009 Sep;149A(9):1885-93. doi: 10.1002/ajmg.a.32761. Am J Med Genet A. 2009. PMID: 19353643 Free PMC article.

3

Growth characteristics of children with ectodermal dysplasia syndromes.

Motil KJ, Fete TJ, Fraley JK, Schultz RJ, Foy TM, Ochs U, Sybert VP. Motil KJ, et al. Among authors: sybert vp. Pediatrics. 2005 Aug;116(2):e229-34. doi: 10.1542/peds.2004-2830. Pediatrics. 2005. PMID: 16061575

4

Skin erosions and wound healing in ankyloblepharon-ectodermal defect-cleft lip and/or palate.

Siegfried E, Bree A, Fete M, Sybert VP. Siegfried E, et al. Among authors: sybert vp. Arch Dermatol. 2005 Dec;141(12):1591-4. doi: 10.1001/archderm.141.12.1591. Arch Dermatol. 2005. PMID: 16365264 Review. No abstract available.

5

Dermatologic findings of ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) syndrome.

Julapalli MR, Scher RK, Sybert VP, Siegfried EC, Bree AF. Julapalli MR, et al. Among authors: sybert vp. Am J Med Genet A. 2009 Sep;149A(9):1900-6. doi: 10.1002/ajmg.a.32797. Am J Med Genet A. 2009. PMID: 19681128

6

Early diagnosis in the ectodermal dysplasias.

Sybert VP. Sybert VP. Birth Defects Orig Artic Ser. 1988;24(2):277-8. Birth Defects Orig Artic Ser. 1988. PMID: 3179432 No abstract available.

7

Definitive evidence for an autosomal recessive form of hypohidrotic ectodermal dysplasia clinically indistinguishable from the more common X-linked disorder.

Munoz F, Lestringant G, Sybert V, Frydman M, Alswaini A, Frossard PM, Jorgenson R, Zonana J. Munoz F, et al. Am J Hum Genet. 1997 Jul;61(1):94-100. doi: 10.1086/513905. Am J Hum Genet. 1997. PMID: 9245989 Free PMC article.

8

Postnatal outcomes of prenatally diagnosed 45,X/46,XX.

Tokita MJ, Sybert VP. Tokita MJ, et al. Among authors: sybert vp. Am J Med Genet A. 2016 May;170A(5):1196-201. doi: 10.1002/ajmg.a.37551. Epub 2016 Jan 20. Am J Med Genet A. 2016. PMID: 26789280

9

Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis.

Kelsell DP, Norgett EE, Unsworth H, Teh MT, Cullup T, Mein CA, Dopping-Hepenstal PJ, Dale BA, Tadini G, Fleckman P, Stephens KG, Sybert VP, Mallory SB, North BV, Witt DR, Sprecher E, Taylor AE, Ilchyshyn A, Kennedy CT, Goodyear H, Moss C, Paige D, Harper JI, Young BD, Leigh IM, Eady RA, O'Toole EA. Kelsell DP, et al. Among authors: sybert vp. Am J Hum Genet. 2005 May;76(5):794-803. doi: 10.1086/429844. Epub 2005 Mar 8. Am J Hum Genet. 2005. PMID: 15756637 Free PMC article.

10

Hypohidrotic ectodermal dysplasia: argument against an autosomal recessive form clinically indistinguishable from X-linked hypohidrotic ectodermal dysplasia (Christ-Siemens-Touraine syndrome).

Sybert VP. Sybert VP. Pediatr Dermatol. 1989 Jun;6(2):76-81. doi: 10.1111/j.1525-1470.1989.tb01002.x. Pediatr Dermatol. 1989. PMID: 2748478

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