TY  - GEN
AU  - Thevenon,Julien
AU  - Callier,Patrick
AU  - Thauvin-Robinet,Christel
AU  - Mejean,Nathalie
AU  - Falcon-Eicher,Sylvie
AU  - Maynadie,Marc
AU  - de Maistre,Emmanuel
AU  - Bidot,Samuel
AU  - Huet,Frédéric
AU  - Beri-Dexheimer,Mylène
AU  - Jonveaux,Philippe
AU  - Mugneret,Francine
AU  - Faivre,Laurence
TI  - De Novo 21q22.1q22.2 deletion including RUNX1 mimicking a congenital infection
SN  - 1552-4833
PY  - 2011///0517
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Child
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 21
KW  - Core Binding Factor Alpha 2 Subunit
KW  - Diagnosis, Differential
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Phenotype
KW  - Syndrome
KW  - Thrombocytopenia
N1  - Publication Type: Case Reports; Comment; Letter
UR  - https://doi.org/10.1002/ajmg.a.33809
ER  -