Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1)

Eberhard Schwinger; Koen Devriendt; Anita Rauch; Nicole Philip

doi:10.1038/ejhg.2010.5

Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1)

Eberhard Schwinger^*, Koen Devriendt, Anita Rauch, Nicole Philip

^*Corresponding author for this work

Original language	English
Journal	European Journal of Human Genetics
Volume	18
Issue number	9
Number of pages	1
ISSN	1018-4813
DOIs	https://doi.org/10.1038/ejhg.2010.5
Publication status	Published - 01.09.2010
Externally published	Yes

Research Areas and Centers

Research Area: Medical Genetics

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10.1038/ejhg.2010.5

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title = "Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1)",

author = "Eberhard Schwinger and Koen Devriendt and Anita Rauch and Nicole Philip",

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language = "English",

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AU - Schwinger, Eberhard

AU - Devriendt, Koen

AU - Rauch, Anita

AU - Philip, Nicole

PY - 2010/9/1

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DO - 10.1038/ejhg.2010.5

M3 - Short survey

C2 - 20125192

AN - SCOPUS:77955982898

SN - 1018-4813

VL - 18

JO - European Journal of Human Genetics

JF - European Journal of Human Genetics

IS - 9

ER -

Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1)

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