OPITZ-SYNDROME, A DEFECT OF MIDLINE DEVELOPMENT, IS DUE TO MUTATIONS IN A NOVEL RING FINGER GENE ON XP22

QUADERI NA SCHWEIGER S GAUDENZ K FRANCO B RUGARLI E FELDMAN GJ VOLTA M GILGENKRANTZ S BERGER W OPITZ J MUENCKE J ROPERS H BALLABIO A

Na. Quaderi et al., OPITZ-SYNDROME, A DEFECT OF MIDLINE DEVELOPMENT, IS DUE TO MUTATIONS IN A NOVEL RING FINGER GENE ON XP22, American journal of human genetics, 61(4), 1997, pp. 44-44

NO

American journal of human genetics → ACNP

00029297

61

4

1997

S

44 - 44

ISI

0002-9297(1997)61:4<44:OADOMD>2.0.ZU;2-T