TY  - GEN
AU  - Lezirovitz,Karina
AU  - Nicastro,Fernanda Stávale
AU  - Pardono,Eliete
AU  - Abreu-Silva,Ronaldo Serafim
AU  - Batissoco,Ana Carla
AU  - Neustein,Isaac
AU  - Spinelli,Mauro
AU  - Mingroni-Netto,Regina Célia
TI  - Is autosomal recessive deafness associated with oculocutaneous albinism a "coincidence syndrome"?
SN  - 1434-5161
PY  - 2006///1006
KW  - Adolescent
KW  - Albinism, Oculocutaneous
KW  - complications
KW  - Antigens, Neoplasm
KW  - Audiometry, Pure-Tone
KW  - Child
KW  - Child, Preschool
KW  - Connexin 26
KW  - Connexins
KW  - DNA Mutational Analysis
KW  - Deafness
KW  - Exons
KW  - genetics
KW  - Female
KW  - Genes, Recessive
KW  - Haplotypes
KW  - Heterozygote
KW  - Humans
KW  - Male
KW  - Membrane Proteins
KW  - Membrane Transport Proteins
KW  - Molecular Sequence Data
KW  - Pedigree
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1007/s10038-006-0003-7
ER  -