An unique case of a mosaic genome-wide uniparental isodisomy in a newborn with Beckwith-Wiedemann syndrome

LTJN van der Veken; P. Hochstenbach; AA Verrijn Stuart; JC Giltay; SMJ Hopman

An unique case of a mosaic genome-wide uniparental isodisomy in a newborn with Beckwith-Wiedemann syndrome

LTJN van der Veken, P. Hochstenbach, AA Verrijn Stuart, JC Giltay, SMJ Hopman

Research output: Contribution to conference › Poster › Other research output

Original language	English
Publication status	Published - 2016
Event	13th International Congress of Human Genetics (ICHG2016): “Frontier of Genomic Medicine: Message from the Past to the Future.” - Kyoto International Conference Center, Annex 2, Kyoto, Japan Duration: 3 Apr 2016 → 7 Apr 2016 Conference number: 13th http://www.ichg2016.org/

Conference

Conference	13th International Congress of Human Genetics (ICHG2016)
Abbreviated title	ICHG2016
Country/Territory	Japan
City	Kyoto
Period	3/04/16 → 7/04/16
Internet address	http://www.ichg2016.org/

Cite this

@conference{13911e9e24214add832573547406a332,

title = "An unique case of a mosaic genome-wide uniparental isodisomy in a newborn with Beckwith-Wiedemann syndrome",

author = "\{van der Veken\}, LTJN and P. Hochstenbach and \{Verrijn Stuart\}, AA and JC Giltay and SMJ Hopman",

year = "2016",

language = "English",

note = "13th International Congress of Human Genetics (ICHG2016) : “Frontier of Genomic Medicine: Message from the Past to the Future.”, ICHG2016 ; Conference date: 03-04-2016 Through 07-04-2016",

url = "http://www.ichg2016.org/",

}

TY - CONF

T1 - An unique case of a mosaic genome-wide uniparental isodisomy in a newborn with Beckwith-Wiedemann syndrome

AU - van der Veken, LTJN

AU - Hochstenbach, P.

AU - Verrijn Stuart, AA

AU - Giltay, JC

AU - Hopman, SMJ

N1 - Conference code: 13th

PY - 2016

Y1 - 2016

M3 - Poster

T2 - 13th International Congress of Human Genetics (ICHG2016)

Y2 - 3 April 2016 through 7 April 2016

ER -