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Volumn 34, Issue 2, 1996, Pages 223-225
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Assembly of a 1-Mb restriction-mapped cosmid contig spanning the candidate region for finnish congenital nephrosis (NPHS1) in 19q13.1
a a a a |
Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENTARY DNA;
ARTICLE;
CHROMOSOME 19Q;
CONGENITAL NEPHROTIC SYNDROME;
DNA FINGERPRINTING;
DNA LIBRARY;
HUMAN;
HUMAN CELL;
HUMAN TISSUE;
MOLECULAR CLONING;
PRIORITY JOURNAL;
PROTEIN ASSEMBLY;
RESTRICTION MAPPING;
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EID: 0029895533
PISSN: 08887543
EISSN: None
Source Type: Journal
DOI: 10.1006/geno.1996.0270 Document Type: Article |
Times cited : (15)
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References (0)
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