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Ophthalmic Genetics

Volumn 22, Issue 1, 2001, Pages 1-10

Molecular characterization of the deletion in retinoblastoma patients with 13q14 cytogenetic anomalies

(6) Lavanchy, L a Munier, F L a Cousin, P a Gaide, A C a Thonney, F a Schorderet, D F a

a LAUSANNE UNIVERSITY HOSPITAL (Switzerland)

Author keywords

Chromosome 13; Cytogenetic deletion; Mapping; Retinoblastoma

Indexed keywords

ARTICLE; CHILD; CHROMOSOME 13Q; CLINICAL ARTICLE; CYTOGENETICS; EYE TUMOR; FEMALE; GENE DELETION; GENE MAPPING; GENETIC ANALYSIS; GENETIC DISORDER; GENETIC MARKER; HUMAN; INFANT; MALE; PATIENT CODING; PRIORITY JOURNAL; RETINOBLASTOMA;

CHILD, PRESCHOOL; CHROMOSOME FRAGILITY; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 13; CLONE CELLS; DNA; FACIES; FEMALE; GENE DELETION; GENETIC MARKERS; HUMANS; INFANT; MALE; RETINAL NEOPLASMS; RETINOBLASTOMA; SYNDROME;

EID: 0035082596 PISSN: 13816810 EISSN: None Source Type: Journal
DOI: 10.1076/opge.22.1.1.2236 Document Type: Article

Times cited : (7)

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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.