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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Detalhes bibliográficos
Publicado no: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
Formato: Artigo
Idioma:Inglês
Publicado em: Hindawi 2019
Assuntos:
Case Report
Acesso em linha: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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