BAP1 Tumour Predisposition Syndrome: A New Mutation in One Family

Acta Dermato-Venereologica - Sweden
doi 10.2340/00015555-3267
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Acta Dermato-Venereologica

Related search

A New Family With a germlineANKRD26mutation and Predisposition to Myeloid Malignancies

Leukemia and Lymphoma
Cancer ResearchOncologyHematology
2014English

A Family With Sertoli–Leydig Cell Tumour, Multinodular Goiter, and DICER1 Mutation

Current Oncology
Oncology
2019English

A Novel Mutation in a Kazakh Family With X-Linked Alport Syndrome

PLoS ONE
Multidisciplinary
2015English

Peutz-Jeghers Syndrome: Four Cases in One Family

Intractable and Rare Diseases Research
Medicine
2015English

Pathogenic Effect of a TGFBR1 Mutation in a Family With Loeys–Dietz Syndrome

Molecular genetics & genomic medicine
GeneticsMolecular Biology
2019English

A Family With Liddle's Syndrome Caused by a New C.1721 Deletion Mutation in the Epithelial Sodium Channel Β‑subunit

Experimental and Therapeutic Medicine
MedicineCancer ResearchImmunologyMicrobiology
2019English

Identification of a Novel TCOF1 Mutation in a Chinese Family With Treacher Collins Syndrome

Experimental and Therapeutic Medicine
MedicineCancer ResearchImmunologyMicrobiology
2018English

A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report

Frontiers in Genetics
GeneticsMolecular Medicine
2020English

Exome Sequencing Identified New Mutations in a Marfan Syndrome Family

Diagnostic Pathology
Forensic MedicineMedicinePathologyHistology
2014English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy