MED12, the Mediator Complex Subunit 12 Gene, Is Mutated at High Frequency in Uterine Leiomyomas

Mary Lyon and the hypothesis of random X chromosome inactivation

(2011) Peter S. Harper   HUMAN GENETICS

Behavioral features in young adults with FG syndrome (Opitz-Kaveggia syndrome)

(2010) John M. Graham et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART C-SEMINARS IN MEDICAL GENETICS

Fusion of HMGA2 to COG5 in uterine leiomyoma

(2010) Gopalrao V.N. Velagaleti et al.   CANCER GENETICS AND CYTOGENETICS

A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome)

(2010) P Rump et al.   CLINICAL GENETICS

Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling

(2010) P. P. Rocha et al.   DEVELOPMENT

The human Mediator complex: a versatile, genome-wide regulator of transcription

(2010) Dylan J. Taatjes   TRENDS IN BIOCHEMICAL SCIENCES

Nationwide Use of Laparoscopic Hysterectomy Compared With Abdominal and Vaginal Approaches

(2009) Vanessa L. Jacoby et al.   OBSTETRICS AND GYNECOLOGY

Incidence, aetiology and epidemiology of uterine fibroids

(2008) Stanley Okolo   BEST PRACTICE & RESEARCH CLINICAL OBSTETRICS & GYNAECOLOGY

Comparative genomics supports a deep evolutionary origin for the large, four-module transcriptional mediator complex

(2008) Henri-Marc Bourbon   NUCLEIC ACIDS RESEARCH