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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Bibliographische Detailangaben
Veröffentlicht in:Case Rep Obstet Gynecol
Hauptverfasser: Toshimitsu, Masatake, Nagaoka, Shinichi, Kobori, Shuusaku, Ogawa, Maki, Suzuki, Fumihiko, Kato, Takema, Miyai, Shunsuke, Kawamura, Rie, Inagaki, Hidehito, Kurahashi, Hiroki, Murotsuki, Jun
Format: Artigo
Sprache:Inglês
Veröffentlicht: Hindawi 2019
Schlagworte:
Case Report
Online Zugang: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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