TY  - GEN
AU  - Taschner,P E
AU  - de Vos,N
AU  - Thompson,A D
AU  - Callen,D F
AU  - Doggett,N
AU  - Mole,S E
AU  - Dooley,T P
AU  - Barth,P G
AU  - Breuning,M H
TI  - Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease)
SN  - 0002-9297
PY  - 1995///0413
KW  - Alleles
KW  - Base Sequence
KW  - Child
KW  - Chromosome Mapping
KW  - Chromosomes, Human, Pair 16
KW  - Haplotypes
KW  - Humans
KW  - Male
KW  - Molecular Sequence Data
KW  - Neuronal Ceroid-Lipofuscinoses
KW  - genetics
KW  - Pedigree
KW  - Polymerase Chain Reaction
KW  - Sequence Deletion
N1  - Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
ER  -