Partial deletion of DMRT1 causes 46,XY ovotesticular disorder of sexual development

Novel DMRT1 3'UTR+11insT mutation associated to XY partial gonadal dysgenesis

(2011) Maricilda Palandi de Mello et al.   Arquivos Brasileiros de Endocrinologia e Metabologia

DMRT1 prevents female reprogramming in the postnatal mammalian testis

(2011) Clinton K. Matson et al.   NATURE

The Mammalian Doublesex Homolog DMRT1 Is a Transcriptional Gatekeeper that Controls the Mitosis versus Meiosis Decision in Male Germ Cells

(2010) Clinton K. Matson et al.   DEVELOPMENTAL CELL

Array-CGH analysis in patients with syndromic and non-syndromic XY gonadal dysgenesis: evaluation of array CGH as diagnostic tool and search for new candidate loci

(2010) S. Ledig et al.   HUMAN REPRODUCTION

Genome-wide analysis of DNA binding and transcriptional regulation by the mammalian Doublesex homolog DMRT1 in the juvenile testis

(2010) M. W. Murphy et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

The DM domain protein DMRT1 is a dose-sensitive regulator of fetal germ cell proliferation and pluripotency

(2009) Anthony D. Krentz et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Syndromic true hermaphroditism due to an R-spondin1 (RSPO1) homozygous mutation

(2007) Sara Tomaselli et al.   HUMAN MUTATION

XX Maleness and XX True Hermaphroditism inSRY-Negative Monozygotic Twins: Additional Evidence for a Common Origin

(2007) Andréa Trevas Maciel-Guerra et al.   JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM