Publications:

Exome sequencing of 85 Williams-Beuren syndrome cases rules out coding variation as a major contributor to remaining variance in social behavior.

Molecular Genetics & Genomic Medicine

Kopp, Nathan D ND; Parrish, Phoebe C R PCR; Lugo, Michael M; Dougherty, Joseph D JD; Kozel, Beth A BA

Publication Date: 2018-09

Variant appearance in text: rs72470514

PubMed Link: 30008175

Variant Present in the following documents:

• MGG3-6-749-s004.xlsx, sheet 1

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Sporadic hemangioblastomas are characterized by cryptic VHL inactivation.

Acta Neuropathologica Communications

Shankar, Ganesh M GM; Taylor-Weiner, Amaro A; Lelic, Nina N; Jones, Robert T RT; Kim, James C JC; Francis, Joshua M JM; Abedalthagafi, Malak M; Borges, Lawrence F LF; Coumans, Jean-Valery JV; Curry, William T WT; Nahed, Brian V BV; Shin, John H JH; Paek, Sun Ha SH; Park, Sung-Hye SH; Stewart, Chip C; Lawrence, Michael S MS; Cibulskis, Kristian K; Thorner, Aaron R AR; Van Hummelen, Paul P; Stemmer-Rachamimov, Anat O AO; Batchelor, Tracy T TT; Carter, Scott L SL; Hoang, Mai P MP; Santagata, Sandro S; Louis, David N DN; Barker, Fred G FG; Meyerson, Matthew M; Getz, Gad G; Brastianos, Priscilla K PK; Cahill, Daniel P DP

Publication Date: 2014-12-24

Variant appearance in text: rs72470514

PubMed Link: 25589003

Variant Present in the following documents:

• 40478_2014_167_MOESM1_ESM.xlsx, sheet 6

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The dystrophin gene and cognitive function in the general population.

European Journal Of Human Genetics : Ejhg

Vojinovic, Dina D; Adams, Hieab H H HH; van der Lee, Sven J SJ; Ibrahim-Verbaas, Carla A CA; Brouwer, Rutger R; van den Hout, Mirjam C G N MC; Oole, Edwin E; van Rooij, Jeroen J; Uitterlinden, Andre A; Hofman, Albert A; van IJcken, Wilfred F J WF; Aartsma-Rus, Annemieke A; van Ommen, GertJan B GB; Ikram, M Arfan MA; van Duijn, Cornelia M CM; Amin, Najaf N

Publication Date: 2015-06

Variant appearance in text: rs72470514

PubMed Link: 25227141

Variant Present in the following documents:

• Main text

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