Chromosome 16 microdeletion in a patient with juvenile neuronal ceroid lipofuscinosis (Batten disease)

American Journal of Human Genetics

Volumn 56, Issue 3, 1995, Pages 663-668

  Taschner, P E M ^a   De Vos, N ^a   Thompson, A D ^a   Callen, D F ^a   Doggett, N ^a   Mole, S E ^a   Dooley, T P ^a   Barth, P G ^a   Breuning, M H ^a  

^a LEIDEN UNIVERSITY   (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

SULFOTRANSFERASE;

ARTICLE; CHROMOSOME 16; CONSANGUINEOUS MARRIAGE; DNA FLANKING REGION; DNA PROBE; GENE DELETION; GENE LOCATION; GENE MUTATION; GENE SEQUENCE; HAPLOTYPE; HUMAN; HUMAN CELL; MULTIGENE FAMILY; NEURONAL CEROID LIPOFUSCINOSIS; PRIORITY JOURNAL;

ALLELES; BASE SEQUENCE; CASE REPORT; CHILD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 16; HAPLOTYPES; HUMAN; MALE; MOLECULAR SEQUENCE DATA; NEURONAL CEROID-LIPOFUSCINOSIS; PEDIGREE; POLYMERASE CHAIN REACTION; SEQUENCE DELETION; SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.;

EID: 0028929890     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (0)