Characterization of a novel gene, PNUTL2, on human chromosome 17q22-q23 and its exclusion as the Meckel syndrome gene

Genomics

Volumn 55, Issue 1, 1999, Pages 122-125

  Paavola, Paulina ^a,b   Horelli Kuitunen, Nina ^b   Palotie, Aarno ^b   Peltonen, Leena ^a,b  

^a NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^b UNIVERSITY OF HELSINKI   (Finland)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA;

ARTICLE; CHROMOSOME 17Q; EXPRESSED SEQUENCE TAG; GENE MUTATION; GENETIC ANALYSIS; HUMAN; MECKEL SYNDROME; MULTIGENE FAMILY; NORTHERN BLOTTING; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; SEQUENCE HOMOLOGY;

EID: 0032961592     PISSN: 08887543     EISSN: None     Source Type: Journal    
DOI: 10.1006/geno.1998.5612     Document Type: Article

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