Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance (Q33582763)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance |
scientific article |
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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance (English)
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Gabriele Gillessen-Kaesbach
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Katsuhiko Shirahige
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University of Washington Center for Mendelian Genomics
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Hakon Hakonarson
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Han G Brunner
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Shane McKee
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Louanne Hudgins
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A Micheil Innes
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Zornitza Stark
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Helger Yntema
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Frank J Kaiser
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Morad Ansari
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Diana Braunholz
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María Concepción Gil-Rodríguez
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Christophe Decroos
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Christopher T Fincher
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Maninder Kaur
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Masashige Bando
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Melanie Bahlo
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Christine M Bowman
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Jacquelyn J Bradley
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Dinah Clark
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Miguel Del Campo
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Nataliya Di Donato
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Holly Dubbs
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David A Dyment
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Juliane Eckhold
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Sarah Ernst
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Ulrike Gehlken
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Yolanda Gyftodimou
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Bryan D Hall
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Melanie Hullings
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Jennifer M Hunter
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Antonie D Kline
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Zita Krumina
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Hane Lee
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Kathleen Leppig
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Sally Ann Lynch
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Mark B Mallozzi
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Linda Mannini
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Sarju G Mehta
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Ieva Micule
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Care4Rare Canada Consortium
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Shehla Mohammed
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Ellen Moran
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Joe-Ann S Moser
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Sarah E Noon
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Naohito Nozaki
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Luis Nunes
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Lynette S Penney
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Michael B Petersen
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Beatriz Puisac
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Nicole Revencu
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Elizabeth Roeder
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Sulagna Saitta
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Angela E Scheuerle
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Karen L Schindeler
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Victoria M Siu
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Samuel P Strom
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Heidi Thiese
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Patrick Willems
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Kathleen Williamson
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Louise C Wilson
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Fabiola Quintero-Rivera
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Feliciano J Ramos
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Laird G Jackson
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David W Christianson
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Ian D Krantz
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Matthew A Deardorff
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8 January 2014
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Identifiers
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