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A defect of midline development, Opitz syndrome, is due to mutations in a novel RING finger gene on Xp22
A defect of midline development, Opitz syndrome, is due to mutations in a novel RING finger gene on Xp22
1997
Nandita Quaderi
Susann Schweiger
Karin Gaudenz
Brunella Franco
Elena I. Rugarli
Wolfgang Berger
George J. Feldman
Manuela Volta
Grazia Andolfi
S Gilgenkrantz
Robert W. Marion
Hennekam Rcm.
Jm Opitz
Maximilian Muenke
Hh Ropers
Andrea Ballabio
Keywords:
Biology
Ring finger
Gene
Cell biology
Correction
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