TY  - GEN
AU  - Yan,Denise
AU  - Ouyang,Xiao Mei
AU  - Angeli,Simon I
AU  - Du,Li Lin
AU  - Liu,Xue Zong
TI  - Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss
SN  - 1552-4825
PY  - 2007///0409
KW  - Chromosomes, Human, Pair 13
KW  - Connexin 26
KW  - Connexins
KW  - genetics
KW  - Female
KW  - Gene Frequency
KW  - Hearing Loss
KW  - Homozygote
KW  - Humans
KW  - Male
KW  - Sequence Deletion
KW  - Uniparental Disomy
N1  - Publication Type: Journal Article; Research Support, N.I.H., Extramural
UR  - https://doi.org/10.1002/ajmg.a.31553
ER  -