WordNet

of or relating to a fetus; "fetal development" (同)foetal
underdevelopment of an organ because of a decrease in the number of cells

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1. 先天性肺気道奇形の出生前診断およびマネージメント prenatal diagnosis and management of congenital pulmonary airway malformation
2. 非免疫性胎児水腫 nonimmune hydrops fetalis
3. 子宮内から子宮外の生活への生理的変化 physiologic transition from intrauterine to extrauterine life
4. 胎児異数性に関連する超音波所見 sonographic findings associated with fetal aneuploidy
5. 視神経の先天性および後天性異常 congenital anomalies and acquired abnormalities of the optic nerve

English Journal

A prenatally ascertained, maternally inherited 14.8Mb duplication of chromosomal bands Xq13.2-q21.31 associated with multiple congenital abnormalities in a male fetus.

Sismani C, Donoghue J, Alexandrou A, Karkaletsi M, Christopoulou S, Konstantinidou AE, Livanos P, Patsalis PC, Velissariou V.SourceDepartment of Cytogenetics and Genomics, The Cyprus Institute of Neurology and Genetics, Nicosia, Cyprus.
Gene.Gene.2013 Nov 1;530(1):138-42. doi: 10.1016/j.gene.2013.08.032. Epub 2013 Aug 22.
Duplications of the X chromosome are rare cytogenetic findings, and have been associated with an abnormal phenotype in the male offspring of apparently normal or near normal female carriers. We report on the prenatal diagnosis of a duplication on the long arm of chromosome X from chromosomal band Xq
PMID 23973723

Analysis of microRNA expression profile by small RNA sequencing in Down syndrome fetuses.

Xu Y, Li W, Liu X, Ma H, Tu Z, Dai Y.SourceClinical Medical Research Center, Pingshan People's Hospital, Shenzhen, Guangdong 518118, P.R. China.
International journal of molecular medicine.Int J Mol Med.2013 Nov;32(5):1115-1125. doi: 10.3892/ijmm.2013.1499. Epub 2013 Sep 18.
Down syndrome (DS) is caused by trisomy of human chromosome 21 (Hsa21) and is associated with numerous deleterious phenotypes, including cognitive impairment, childhood leukemia and immune defects. Five Hsa21‑derived microRNAs (i.e., hsa-miR-99a, let-7c, miR-125b-2, miR-155 and miR-802) are invol
PMID 24071828

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