A Case of Partial 14q- with Facial Features of Holoprosencephaly and Hydranencephaly

Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-paired

Stephen Brown, Dorothy Warburton, Lucia Brown et al. · Nature Genetics · 1998 · 521 citations

Biology, Developmental Biology, Developmental Genetics +7

Mutations in the homeodomain of the human SIX3 gene cause holoprosencephaly

Deeann Wallis, Erich Roessler, Ute Hehr et al. · Nature Genetics · 1999 · 427 citations

Developmental Biology, Genetic Disorder, Genetics +4

Mutations in TGIF cause holoprosencephaly and link NODAL signalling to human neural axis determination

Karen W. Gripp, David Wotton, Michael C. Edwards et al. · Nature Genetics · 2000 · 390 citations

Developmental Biology, Molecular Neuroscience, Neurogenomics +11

Defining a holoprosencephaly locus on human chromosome 14q13 and characterization of potential candidate genes

Deepak Kamnasaran, Chih‐Ping Chen, Koenraad Devriendt et al. · Genomics · 2005 · 41 citations

Holoprosencephaly Locus, Developmental Biology, Cytogenetics +8

The Novel Genetic Disorder Microhydranencephaly Maps to Chromosome 16p13.3-12.1

G. N. KAVASLAR, Suna Önengüt, Orhan Derman et al. · The American Journal of Human Genetics · 2000 · 29 citations · Full text

Medicine, Genetics, Chromosome Dynamics +1