DMRTA2 (DMRT5) is mutated in a novel cortical brain malformation

ClinGen — The Clinical Genome Resource

(2015) Heidi L. Rehm et al.   NEW ENGLAND JOURNAL OF MEDICINE

The genetics of lissencephaly

(2014) Andrew E. Fry et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Germline Mutations inSUFUCause Gorlin Syndrome–Associated Childhood Medulloblastoma and Redefine the Risk Associated WithPTCH1Mutations

(2014) Miriam J. Smith et al.   JOURNAL OF CLINICAL ONCOLOGY

Transcriptional landscape of the prenatal human brain

(2014) Jeremy A. Miller et al.   NATURE

Growth and folding of the mammalian cerebral cortex: from molecules to malformations

(2014) Tao Sun et al.   NATURE REVIEWS NEUROSCIENCE

The Doublesex Homolog Dmrt5 is Required for the Development of the Caudomedial Cerebral Cortex in Mammals

(2012) Amandine Saulnier et al.   CEREBRAL CORTEX

The Xenopus doublesex-related gene Dmrt5 is required for olfactory placode neurogenesis

(2012) Damien Parlier et al.   DEVELOPMENTAL BIOLOGY

The Mammalian DM Domain Transcription Factor Dmrta2 Is Required for Early Embryonic Development of the Cerebral Cortex

(2012) Daijiro Konno et al.   PLoS One

Identification and Characterization of an Inborn Error of Metabolism Caused by Dihydrofolate Reductase Deficiency

(2011) Siddharth Banka et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Zebrafish Dmrta2 regulates neurogenesis in the telencephalon

(2011) Akio Yoshizawa et al.   GENES TO CELLS

TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins

(2010) Ravinesh A. Kumar et al.   HUMAN MOLECULAR GENETICS