Multiple congenital anomalies associated with oral anticoagulants

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Immunology today·2014

Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype.

Clinical genetics·2013

Absence of binding of alpha-bungarotoxin and cobra neurotoxin to central acetylcholine receptors - an autoradiographic study.

Neuroscience letters·2009

The importance of the fetal origins of adult disease for geneticists.

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American journal of obstetrics and gynecology·2026

Women with cerebral palsy receive significantly less gynecologic preventative care.

American journal of obstetrics and gynecology·2026

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American journal of obstetrics and gynecology·2026

Feasibility of Fetoscopic Spina Bifida Repair Using a Human Umbilical Cord Meningeal Patch: A Nonrandomized Clinical Trial.

American journal of obstetrics and gynecology·2026

Development and clinical validation of an objective assessment tool for robotic-assisted and laparoscopic hysterectomy.

American journal of obstetrics and gynecology·2026

Clinical and histological chorioamnionitis, particularly when associated with funisitis, attenuate intrapartum fetal heart rate responses and increase vulnerability to hypoxic-ischemic brain injury at milder degrees of acidemia.

American journal of obstetrics and gynecology·2026

Consolidation Therapy Based on Mutation Clearance in Acute Myeloid Leukemia.

NEJM evidence·2026

Heart Failure and Cancer: Incidence and Mortality Patterns, A Systematic Review and Meta-analysis.

European journal of heart failure·2026

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European journal of haematology·2026

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Case reports in pediatrics·2026

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Oncology letters·2026

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Immunometabolism (Cobham, Surrey)·2026

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Multiple congenital anomalies associated with oral anticoagulants

Related Concept Videos

Preservation of erniettomorph fossils in clay-rich siliciclastic deposits from the Ediacaran Wood Canyon Formation, Nevada.

The early history of Pallister-Hall syndrome-Buried treasure of a sort.

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Exome sequencing identifies mutations in KIF14 as a novel cause of an autosomal recessive lethal fetal ciliopathy phenotype.

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Multiple congenital anomalies associated with oral anticoagulants

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