Mosaic Trisomy 7
What's New
Last Posted: Feb 27, 2023
- [Genetic analysis of a case of mosaic trisomy 21 associated with autism spectrum disorder].
Yan Dongmei, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2020 0 (2) 190-194 - Identification of aneuploidy in dogs screened by a SNP microarray.
Shaffer Lisa G, et al. Human genetics 2021 0 (11) 1619-1624 - Different effects of maternal homocysteine concentration, MTHFR and MTRR genetic polymorphisms on the occurrence of fetal aneuploidy.
Guo Qian-Nan, et al. Reproductive biomedicine online 2022 7 - Chromosomal Numerical Aberrations and Rare Copy Number Variation in Patients with Inflammatory Bowel Disease.
Dirvanskyte Paulina, et al. Journal of Crohn's & colitis 2022 7 - Mosaic trisomy 17 at amniocentesis: Prenatal diagnosis, molecular genetic analysis, and literature review.
Chen Chih-Ping et al. Taiwanese journal of obstetrics & gynecology 2016 Oct (5) 712-717 - SNP microarray abnormalities in a cohort of 28 infants with congenital diaphragmatic hernia.
Stark Zornitza, et al. American journal of medical genetics. Part A 2015 10 (10) 2319-26 - Mosaic trisomy 13
From NCATS Genetic and Rare Diseases Information Center - Mosaic trisomy 14
From NCATS Genetic and Rare Diseases Information Center - Mosaic trisomy 22
From NCATS Genetic and Rare Diseases Information Center - Mosaic trisomy 6
From NCATS Genetic and Rare Diseases Information Center - Mosaic trisomy 7
From NCATS Genetic and Rare Diseases Information Center - Mosaic trisomy 8
From NCATS Genetic and Rare Diseases Information Center - Mosaic trisomy 9
From NCATS Genetic and Rare Diseases Information Center
About Rare Diseases PHGKB
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
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
- Content source: