Characterization of a Novel Gene,PNUTL2,on Human Chromosome 17q22-q23 and Its Exclusion as the Meckel Syndrome Gene

Author: Paavola P.   Horelli-Kuitunen N.   Palotie A.   Peltonen L.  

Publisher: Elsevier

ISSN: 0888-7543

Source: Genomics, Vol.55, Iss.1, 1999-01, pp. : 122-125

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