TY  - GEN
AU  - Delahaye,Andrée
AU  - Khung-Savatovsky,Suonavy
AU  - Aboura,Azzedine
AU  - Guimiot,Fabien
AU  - Drunat,Séverine
AU  - Alessandri,Jean-Luc
AU  - Gérard,Marion
AU  - Bitoun,Pierre
AU  - Boumendil,Julien
AU  - Robin,Stéphanie
AU  - Huel,Chan
AU  - Guilherme,Romain
AU  - Serero,Stéphane
AU  - Gressens,Pierre
AU  - Elion,Jacques
AU  - Verloes,Alain
AU  - Benzacken,Brigitte
AU  - Delezoide,Anne-Lise
AU  - Pipiras,Eva
TI  - Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene
SN  - 1552-4833
PY  - 2013///0219
KW  - Adult
KW  - Anterior Eye Segment
KW  - abnormalities
KW  - Cerebellar Diseases
KW  - genetics
KW  - Child, Preschool
KW  - Chromosomes, Human, Pair 6
KW  - Comparative Genomic Hybridization
KW  - Dandy-Walker Syndrome
KW  - Eye Abnormalities
KW  - Eye Diseases, Hereditary
KW  - Female
KW  - Fetus
KW  - pathology
KW  - Forkhead Transcription Factors
KW  - Gene Deletion
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Male
KW  - Phenotype
KW  - Pregnancy
N1  - Publication Type: Journal Article
UR  - https://doi.org/10.1002/ajmg.a.35548
ER  -