Embryonal Carcinoma
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Last Posted: Mar 15, 2023
- Thirty-Year-Old Male Patient with Non-Seminoma and Coincidental Rectal Cancer.
Nolting Julia, et al. Urologia internationalis 2023 0 1-3 - Seminoma component of mixed testicular germ cell tumor shows a higher incidence of loss of heterozygosity than pure-type seminoma.
Miyai Kosuke, et al. Human pathology 2018 0 71-80 - Mediastinal germ cell tumors: many questions and perhaps an answer.
Oosterhuis J Wolter, et al. The Journal of clinical investigation 2020 0 (12) 6238-6241 - 12p gain is predominantly observed in non-germinomatous germ cell tumors and identifies an unfavorable subgroup of central nervous system germ cell tumors.
Satomi Kaishi, et al. Neuro-oncology 2021 0 (5) 834-846 - Histopathology and prognosis of germ cell tumors metastatic to brain: cohort study.
Takami Hirokazu, et al. Journal of neuro-oncology 2021 0 (1) 121-130 - VNTR sequence on human chromosome 11p15 that affects transcriptional activity.
Iwashita S, et al. Journal of human genetics 2002 0 (12) 717-21 - Embryonal carcinoma
From NCATS Genetic and Rare Diseases Information Center - Screening for germline DND1 mutations in testicular cancer patients.
Sijmons Rolf H, et al. Familial cancer 2010 9 (3) 439-42 - Functional glutathione S-transferase genotypes among testicular germ cell tumor survivors: associations with primary and post-chemotherapy tumor histology.
Kraggerud Sigrid M, et al. Pharmacogenetics and genomics 2009 10 (10) 751-9
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Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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