메뉴 건너뛰기




Volumn 70, Issue 2, 2002, Pages 547-555

A 117-kb microdeletion removing HOXD9-HOXD13 and EVX2 causes synpolydactyly

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; BLOOD SAMPLING; CHROMOSOME BREAKAGE; GENE CLUSTER; GENE DELETION; GENE REARRANGEMENT; GENE TARGETING; GENETIC COUNSELING; HUMAN; HUMAN CELL; LIMB MALFORMATION; MULTIGENE FAMILY; POLYDACTYLY; PRIORITY JOURNAL; SEQUENCE HOMOLOGY;

EID: 0036158262     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/338921     Document Type: Article
Times cited : (90)

References (37)
  • 5
  • 11
    • 0029738552 scopus 로고    scopus 로고
    • A line element is present at the site of a 300-kb deletion starting in intron 10 of the PAX6 gene in a case of familial aniridia
    • (1996) Hum Genet , vol.98 , pp. 297-303
    • Drechsler, M.1    Royer-Pokora, B.2
  • 17
    • 2042437650 scopus 로고    scopus 로고
    • Initial sequencing and analysis of the human genome
    • (2001) Nature , vol.409 , pp. 860-921
  • 19
    • 0027953771 scopus 로고
    • Hox genes in vertebrate development
    • (1994) Cell , vol.78 , pp. 191-201
    • Krumlauf, R.1
  • 37
    • 0032902095 scopus 로고    scopus 로고
    • Hox genes in digit development and evolution
    • Cell Tissue Res , vol.296 , pp. 19-25


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.