Association between mutation of the NF2 gene and monosomy 22 in menopausal women with sporadic meningiomas

BMC Medical Genetics

Volumn 14, Issue 1, 2013, Pages

  Tabernero, MariaDolores ^a,b,c   Jara Acevedo, María ^b,c   Nieto, Ana B ^b,c   Caballero, Arancha R ^b,c   Otero, Álvaro ^b,d   Sousa, Pablo ^b,d   Gonçalves, Jesús ^b,d   Domingues, Patricia H ^b,c   Orfao, Alberto ^b,c  

^a Instituto de Ciencias de la Salud de Castilla y León IECSCYL   (Spain)

^b INSTITUTO DE INVESTIGACIÓN BIOMÉDICA DE SALAMANCA IBSAL   (Spain)

^c CSIC   (Spain)

^d HOSPITAL UNIVERSITARIO DE SALAMANCA   (Spain)

Author keywords

Menopausal women; Monosomy 22; Mutation; NF2 gene; Sporadic meningiomas

Indexed keywords

MERLIN;

ADULT; AGED; ARTICLE; CHROMOSOME 22; CLINICAL ARTICLE; DNA EXTRACTION; EXON; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MUTATION; GENETIC ASSOCIATION; HETEROZYGOSITY LOSS; HUMAN; MALE; MENINGIOMA; MENOPAUSE; MONOSOMY; SINGLE NUCLEOTIDE POLYMORPHISM; SPORADIC MENINGIOMA;

AGED; CHROMOSOME DELETION; CHROMOSOMES, HUMAN, PAIR 22; EXONS; FEMALE; GENE DOSAGE; HUMANS; LOSS OF HETEROZYGOSITY; MALE; MENINGEAL NEOPLASMS; MENINGIOMA; MENOPAUSE; MIDDLE AGED; MONOSOMY; MUTATION; MUTATION RATE; NEUROFIBROMIN 2; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84886490421     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-14-114     Document Type: Article

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