Holoprosencephaly and ZIC2 microdeletions: novel clinical and epidemiological specificities delineated

Description of the smallest critical region for Dandy-Walker malformation in chromosome 13 in a girl with a cryptic deletion related to t(6;13)(q23;q32)

(2010) Irene Mademont-Soler et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Analysis of genotype-phenotype correlations in human holoprosencephaly

(2010) Benjamin D. Solomon et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Holoprosencephaly: recommendations for diagnosis and management

(2010) Emily F Kauvar et al.   CURRENT OPINION IN PEDIATRICS

The unfolding clinical spectrum of holoprosencephaly due to mutations in SHH, ZIC2, SIX3 and TGIF genes

(2010) Aimée DC Paulussen et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Phenotype and 244k array-CGH characterization of chromosome 13q deletions: An update of the phenotypic map of 13q21.1-qter

(2009) Maria Kirchhoff et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

Zebrafish zic2a patterns the forebrain through modulation of Hedgehog-activated gene expression

(2009) N. A. Sanek et al.   DEVELOPMENT

A novel genetic mechanism regulates dorsolateral hinge-point formation during zebrafish cranial neurulation

(2009) M. K. Nyholm et al.   JOURNAL OF CELL SCIENCE

Mutations in ZIC2 in human holoprosencephaly: description of a Novel ZIC2 specific phenotype and comprehensive analysis of 157 individuals

(2009) B. D. Solomon et al.   JOURNAL OF MEDICAL GENETICS

Twelve new patients with 13q deletion syndrome: Genotype–phenotype analyses in progress

(2008) Chloé Quélin et al.   European Journal of Medical Genetics

Regulation of a remote Shh forebrain enhancer by the Six3 homeoprotein

(2008) Yongsu Jeong et al.   NATURE GENETICS