Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene.
Delahaye, Andrée
Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene. [electronic resource] - American journal of medical genetics. Part A Oct 2012 - 2430-8 p. digital
Publication Type: Journal Article
1552-4833
10.1002/ajmg.a.35548 doi
Adult
Anterior Eye Segment--abnormalities
Cerebellar Diseases--genetics
Child, Preschool
Chromosomes, Human, Pair 6--genetics
Comparative Genomic Hybridization
Dandy-Walker Syndrome--genetics
Eye Abnormalities--genetics
Eye Diseases, Hereditary
Female
Fetus--pathology
Forkhead Transcription Factors--genetics
Gene Deletion
Humans
In Situ Hybridization, Fluorescence
Male
Phenotype
Pregnancy
Pre- and postnatal phenotype of 6p25 deletions involving the FOXC1 gene. [electronic resource] - American journal of medical genetics. Part A Oct 2012 - 2430-8 p. digital
Publication Type: Journal Article
1552-4833
10.1002/ajmg.a.35548 doi
Adult
Anterior Eye Segment--abnormalities
Cerebellar Diseases--genetics
Child, Preschool
Chromosomes, Human, Pair 6--genetics
Comparative Genomic Hybridization
Dandy-Walker Syndrome--genetics
Eye Abnormalities--genetics
Eye Diseases, Hereditary
Female
Fetus--pathology
Forkhead Transcription Factors--genetics
Gene Deletion
Humans
In Situ Hybridization, Fluorescence
Male
Phenotype
Pregnancy