Nandita Quaderi

Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

Nandita Quaderi, Susann Schweiger, Karin Gaudenz et al. · Nature Genetics · 1997 · 367 citations

Developmental Anomaly, Opitz G/bbb Syndrome, Developmental Biology +7

Expression pattern of the Tbr2 (Eomesodermin) gene during mouse and chick brain development

Alessandro Bulfone, Salvador Martı́nez, Valeria Marigo et al. · Mechanisms of Development · 1999 · 154 citations · Full text

Developmental Biology, Ependyma, Brain Development +9

Isolation, physical mapping, and Northern analysis of the X-linked human gene encoding methyl CpG-binding protein, MECP2

Maurizio D’Esposito, Nandita Quaderi, Alfredo Ciccodicola et al. · Mammalian Genome · 1996 · 138 citations

Chromatin, Methyl Cpg-binding Protein, X-linked Human Gene +11

Opitz G/BBB Syndrome in Xp22: Mutations in the MID1 Gene Cluster in the Carboxy-Terminal Domain

Karin Gaudenz, Erich Roessler, Nandita Quaderi et al. · The American Journal of Human Genetics · 1998 · 69 citations · Full text

Developmental Anomaly, Opitz G/bbb Syndrome, Developmental Biology +10

MID2, a Homologue of the Opitz Syndrome Gene MID1: Similarities in Subcellular Localization and Differences in Expression During Development

Georg Buchner, Eugenio Montini, Grazia Andolfi et al. · Human Molecular Genetics · 1999 · 60 citations · Full text