4.6 Article

Recurrent BCOR internal tandem duplication and BCOR or BCL6 expression distinguish primitive myxoid mesenchymal tumor of infancy from congenital infantile fibrosarcoma

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Article Pathology

BCOR Overexpression Is a Highly Sensitive Marker in Round Cell Sarcomas With BCOR Genetic Abnormalities

Yu-Chien Kao et al.

AMERICAN JOURNAL OF SURGICAL PATHOLOGY (2016)

Article Biochemistry & Molecular Biology

New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs

Dominik Sturm et al.

Article Oncology

Transformation of a Primitive Myxoid Mesenchymal Tumor of Infancy to an Undifferentiated Sarcoma: A First Reported Case

Marie-Christine Guilbert et al.

JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY (2015)

Article Multidisciplinary Sciences

Recurrent internal tandem duplications of BCOR in clear cell sarcoma of the kidney

Angshumoy Roy et al.

NATURE COMMUNICATIONS (2015)

Article Pathology

Primitive Myxoid Mesenchymal Tumor of Infancy With Rosettes: A New Finding and Literature Review

Nicole A. Cipriani et al.

INTERNATIONAL JOURNAL OF SURGICAL PATHOLOGY (2014)

Review Dentistry, Oral Surgery & Medicine

Oculofaciocardiodental Syndrome: A Rare Case and Review of the Literature

Amirparviz Davoody et al.

CLEFT PALATE-CRANIOFACIAL JOURNAL (2012)

Article Genetics & Heredity

A new subtype of bone sarcoma defined by BCOR-CCNB3 gene fusion

Gaelle Pierron et al.

NATURE GENETICS (2012)

Article Pathology

Primitive Myxoid Mesenchymal Tumor of Infancy: A Report of a Further Case with Locally Aggressive Behavior

Linda Mulligan et al.

PEDIATRIC AND DEVELOPMENTAL PATHOLOGY (2011)

Article Dermatology

Primitive Myxoid Mesenchymal Tumor of Infancy in a Preterm Infant

Joseph Lam et al.

PEDIATRIC DERMATOLOGY (2010)

Article Genetics & Heredity

Molecular Characterization of Co-Occurring Duchenne Muscular Dystrophy and X-Linked Oculo-Facio-Cardio-Dental Syndrome in a Girl

Yong-hui Jiang et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2009)

Article Genetics & Heredity

Case reports of oculofaciocardiodental syndrome with unusual dental findings

S Oberoi et al.

AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)

Article Biochemistry & Molecular Biology

Novel mutations in BCOR in three patients with oculo-facio-cardio-dental syndrome, but none in Lenz microphthalmia syndrome

D Horn et al.

EUROPEAN JOURNAL OF HUMAN GENETICS (2005)