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

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

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_dea420e2ab284237a3c92299316b0aae

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

About this item

Full title

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

Publisher

New Zealand: Taylor & Francis Ltd

Journal title

Application of clinical genetics, 2020-01, Vol.13, p.127-137

Language

English

Formats

Publication information

Publisher

New Zealand: Taylor & Francis Ltd

More information

Scope and Contents

Contents

Pediatric germ cell tumors are rare, representing about 3% of childhood malignancies in children less than 15 years of age, presenting in neonates or adolescents with a greater incidence noted in older adolescents. Aberrations in primordial germ cell proliferation/differentiation can lead to a variety of neoplasms, including teratomas, embryonal ca...

Alternative Titles

Full title

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

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_dea420e2ab284237a3c92299316b0aae

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_dea420e2ab284237a3c92299316b0aae

Other Identifiers

ISSN

1178-704X

E-ISSN

1178-704X

DOI

10.2147/TACG.S245093

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