TY  - GEN
AU  - Makrythanasis,Periklis
AU  - Gimelli,Stefania
AU  - Béna,Frédérique
AU  - Dahoun,Sophie
AU  - Morris,Michael A
AU  - Antonarakis,Stylianos E
AU  - Bottani,Armand
TI  - Homozygous deletion of a gene-free region of 4p15 in a child with multiple anomalies: could biallelic loss of conserved, non-coding elements lead to a phenotype?
SN  - 1878-0849
PY  - 2012///0605
KW  - Abnormalities, Multiple
KW  - genetics
KW  - Alleles
KW  - Autistic Disorder
KW  - Base Sequence
KW  - Child, Preschool
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 4
KW  - Cognition Disorders
KW  - Comparative Genomic Hybridization
KW  - Consanguinity
KW  - Conserved Sequence
KW  - Deafness
KW  - Homozygote
KW  - Humans
KW  - Male
KW  - Phenotype
KW  - Polydactyly
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.ejmg.2011.11.001
ER  -