Allelic status of 1p, 14q, and 22q and NF2 gene mutations in sporadic schwannomas.

International journal of molecular medicine

Volumn 1, Issue 5, 1998, Pages 889-892

  Leone, P E ^a   Bello, M J ^a   Mendiola, M ^a   Kusak, M E ^a   De Campos, J M ^a   Vaquero, J ^a   Sarasa, J L ^a   Pestana, A ^a   Rey, J A ^a  

^a INSTITUTO DE INVESTIGACIONES BIOMÉDICAS ALBERTO SOLS   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; ARTICLE; CHROMOSOME 1; CHROMOSOME 14; CHROMOSOME 22; DNA SEQUENCE; GENETIC MARKER; GENETICS; HETEROZYGOSITY LOSS; HUMAN; MUTATION; NEURILEMOMA; NUCLEOTIDE SEQUENCE; TUMOR SUPPRESSOR GENE;

ALLELES; CHROMOSOMES, HUMAN, PAIR 1; CHROMOSOMES, HUMAN, PAIR 14; CHROMOSOMES, HUMAN, PAIR 22; DNA MUTATIONAL ANALYSIS; GENES, NEUROFIBROMATOSIS 2; GENETIC MARKERS; HUMANS; LOSS OF HETEROZYGOSITY; MUTATION; NEURILEMMOMA; SEQUENCE ANALYSIS, DNA;

MLCS; MLOWN;

EID: 0032057239     PISSN: 11073756     EISSN: None     Source Type: Journal    
DOI: 10.3892/ijmm.1.5.889     Document Type: Article

References (0)