<p>Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors</p>-Reference-Cited by-同舟云学术

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Germline Sequencing Identifies Rare Variants in Finnish Subjects with Familial Germ Cell Tumors

Published:2020-06 Issue: Volume:Volume 13 Page:127-137
ISSN:1178-704X
Container-title:The Application of Clinical Genetics
language:en
Short-container-title:TACG

Author:

Crowgey Erin L^ORCID,Soini Tea^ORCID,Shah Nidhi,Pauniaho Satu-Liisa^ORCID,Lahdenne Pekka,Wilson David B^ORCID,Heikinheimo Markku,Druley Todd E^ORCID

Publisher

Informa UK Limited

Subject

Genetics (clinical),Genetics

Reference35 articles.

1. Pediatric and Adolescent Extracranial Germ Cell Tumors: The Road to Collaboration

2. Pediatric Germ Cell Tumors: A Developmental Perspective

3. Variants in BAK1, SPRY4, and GAB2 are associated with pediatric germ cell tumors: a report from the Children’s Oncology GroupHHS Public Access: Genes Chromosome Cancer. 2018;56(7):612–625. doi:10.1002/gcc.22457.Variants

4. Long-term outcomes and late effects for childhood and young adulthood intracranial germinomas

5. Variants in KITLG predispose to testicular germ cell cancer independently from spermatogenic function

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Role of the TEX101 Interactome in the Common Aetiology Behind Male Subfertility and Testicular Germ Cell Tumor;Frontiers in Oncology;2022-06-14

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