TY  - GEN
AU  - Tranebjaerg,L
AU  - Schwartz,C
AU  - Eriksen,H
AU  - Andreasson,S
AU  - Ponjavic,V
AU  - Dahl,A
AU  - Stevenson,R E
AU  - May,M
AU  - Arena,F
AU  - Barker,D
TI  - A new X linked recessive deafness syndrome with blindness, dystonia, fractures, and mental deficiency is linked to Xq22
SN  - 0022-2593
PY  - 1995///0918
KW  - Adolescent
KW  - Adult
KW  - Blindness
KW  - complications
KW  - Child
KW  - Child, Preschool
KW  - Chromosome Mapping
KW  - Deafness
KW  - Dystonia
KW  - Family Health
KW  - Female
KW  - Genes, Recessive
KW  - Genetic Linkage
KW  - Heterozygote
KW  - Humans
KW  - Intellectual Disability
KW  - Male
KW  - Middle Aged
KW  - Nervous System Diseases
KW  - Norway
KW  - Pedigree
KW  - Pregnancy
KW  - Syndrome
KW  - X Chromosome
KW  - genetics
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1136/jmg.32.4.257
ER  -