Novel mutations including deletions of the entire OFD1 gene in 30 families with type 1 orofaciodigital syndrome: a study of the extensive clinical variability (Q33872321)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Novel mutations including deletions of the entire OFD1 gene in 30 families with type 1 orofaciodigital syndrome: a study of the extensive clinical variability |
scientific article |
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Novel mutations including deletions of the entire OFD1 gene in 30 families with type 1 orofaciodigital syndrome: a study of the extensive clinical variability (English)
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Kristina Lagerstedt Robinson
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Christine Zeschnigk
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Denise Horn
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Izak J Bisschoff
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Brigitte Wellek
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Angelika Rieß
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Maja Wessels
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Patrick Willems
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Peter Jensen
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Andreas Busche
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Jens Bekkebraten
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Maya Chopra
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Hanne Dahlgaard Hove
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Christina Evers
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Ann-Sophie Kaiser
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Erdmut Kunstmann
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Maja Linné
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Patricia Martin
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James McGrath
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Winnie Pradel
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Katrina E Prescott
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Bernd Roesler
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Gorazd Rudolf
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Ulrike Siebers-Renelt
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Nataliya Tyshchenko
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Dagmar Wieczorek
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Gerhard Wolff
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Deborah J Morris-Rosendahl
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17 October 2012
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