SCOPUS 정보 검색 플랫폼

Volumn 67, Issue 5, 2000, Pages 1306-1308

Isolation of a cDNA representing the fanconi anemia complementation group E gene

(20) De Winter, Johan P a Léveillé, France a Van Berkel, Carola G M a Rooimans, Martin A a Van Der Weel, Laura a Steltenpool, Jurgen a Demuth, Ilja c Morgan, Neil V d Alon, Noa e Bosnoyan Collins, Lucine e Lightfoot, Jeff e Leegwater, Peter A b Waisfisz, Quinten a Komatsu, Kenshi f Arwert, Fré a Pronk, Jan C a Mathew, Christopher G d Digweed, Martin c Buchwald, Manuel e Joenje, Hans a

a Clinical Genetics and Human Genetics (Netherlands)

b VU UNIVERSITY MEDICAL CENTER (Netherlands)

c HUMBOLDT UNIVERSITY (Germany)

d GUY S HOSPITAL (United Kingdom)

e HOSPITAL FOR SICK CHILDREN (Canada)

f HIROSHIMA UNIVERSITY (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID;

ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CONTROLLED STUDY; EXON; FANCONI ANEMIA; GENE MAPPING; GENE MUTATION; GENETIC COMPLEMENTATION; HUMAN; MOLECULAR CLONING; NUCLEAR LOCALIZATION SIGNAL; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL;

EID: 0033759693 PISSN: 00029297 EISSN: None Source Type: Journal
DOI: 10.1016/S0002-9297(07)62959-0 Document Type: Article

Times cited : (193)

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