NCBI Bookshelf. A service of the National Library of Medicine, National Institutes of Health.
Borgaonkar DS. Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 1975-.
Chromosomal Variation in Man: A Catalog of Chromosomal Variants and Anomalies: Online NLM Version [Internet].
Show details- Ariel I, Lerer I, Yagel S, Cohen R, Ben-Neriah Z, Abeliovich D.: Trisomy 2: confined placental mosaicism in a fetus with intrauterine growth retardation. Prenat. Diag. 17:180-183, 1997. [PubMed: 9061769]Amniocytes=46,XX in 20 colonies.,Placental fibroblasts=47,XX,+2 in 6 colonies.CPM of trisomy 2 is causally related to the IUGR.The placenta was completely trisomic, the trisomy 2 was of paternal origin due to a meiotic I error. The fetus was biparental disomic.Index Terms: CPM
- PubMedLinks to PubMed
- 2+ - Chromosomal Variation in Man2+ - Chromosomal Variation in Man
- Homo sapiens chromosome 19 open reading frame 39, mRNA (cDNA clone MGC:149562 IM...Homo sapiens chromosome 19 open reading frame 39, mRNA (cDNA clone MGC:149562 IMAGE:40116265), complete cdsgi|115527950|gb|BC119677.2|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...