Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome

BACKGROUND: Fetal akinesia refers to a broad spectrum of disorders with reduced or absent fetal movements. There is no established approach for prenatal diagnosis of the cause of fetal akinesia. Chromosome 1p36 deletion syndrome is the most common subtelomeric terminal deletion syndrome, recognized...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Case Rep Obstet Gynecol
Main Authors: Toshimitsu, Masatake, Nagaoka, Shinichi, Kobori, Shuusaku, Ogawa, Maki, Suzuki, Fumihiko, Kato, Takema, Miyai, Shunsuke, Kawamura, Rie, Inagaki, Hidehito, Kurahashi, Hiroki, Murotsuki, Jun
Format: Artigo
Jezik:Inglês
Izdano: Hindawi 2019
Teme:
Case Report
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6791227/
https://ncbi.nlm.nih.gov/pubmed/31662930
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2019/6753184
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