Molecular and clinical delineation of the 17q22 microdeletion phenotype.
Laurell T; Lundin J; Anderlid BM; Gorski JL; Grigelioniene G; Knight SJ; Krepischi AC; Nordenskjöld A; Price SM; Rosenberg C; Turnpenny PD; Vianna-Morgante AM; Nordgren A; European Journal Of Human Genetics: EJHG, 2013, vol. 21, issue 10, p 1085, ISSN 14765438. ISBN 14765438.

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