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Pathogenic variant in NLRP7 (19q13.42) associated with recurrent gestational trophoblastic disease: Data from early embryo development observed during in vitro fertilization
OBJECTIVE: To describe in vitro development of human embryos derived from an individual with a homozygous pathogenic variant in NLRP7 (19q13.42) and recurrent hydatidiform mole (HM), an autosomal recessive condition thought to occur secondary to an oocyte defect. METHODS: A patient with five consecu...
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Publicado no: | Clin Exp Reprod Med |
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Main Authors: | , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
The Korean Society for Reproductive Medicine
2017
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5395551/ https://ncbi.nlm.nih.gov/pubmed/28428943 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5653/cerm.2017.44.1.40 |
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