메뉴 건너뛰기




Volumn 50, Issue 6, 1996, Pages 527-528

Frequent intragenic polymorphism in the 3′ untranslated region of the lissencephaly gene 1 (LIS-1)

Author keywords

[No Author keywords available]

Indexed keywords

DNA MARKER; RESTRICTION ENDONUCLEASE; 1 ALKYL 2 ACETYLGLYCEROPHOSPHOCHOLINE ESTERASE; MICROTUBULE ASSOCIATED PROTEIN; PAFAH1B1 PROTEIN, HUMAN; PROTEIN;

EID: 0030475106     PISSN: 00099163     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1399-0004.1996.tb02728.x     Document Type: Article
Times cited : (6)

References (6)
  • 3
    • 0027486966 scopus 로고
    • Lissencephaly. A human brain malformation associated with deletion of the L1S1 gene located at chromosome 17p13
    • Dobyns WB, Reiner O, Carrozzo R, Ledbetter DH. Lissencephaly. A human brain malformation associated with deletion of the L1S1 gene located at chromosome 17p13. JAMA 1993: 270: 2838-2842.
    • (1993) JAMA , vol.270 , pp. 2838-2842
    • Dobyns, W.B.1    Reiner, O.2    Carrozzo, R.3    Ledbetter, D.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.