Genetic factors in intrauterine growth retardation

Association of human chorionic gonadotropin and post-pregnancy persistent enhanced myometrial vascularity.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2026

United States' experience in nuchal translucency measurement: variation according to provider characteristics in over five million ultrasound examinations.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2021

Accuracy of automated three-dimensional ultrasound imaging technique for fetal head biometry.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2020

Clinical experience of laboratory follow-up with noninvasive prenatal testing using cell-free DNA and positive microdeletion results in 349 cases.

Prenatal diagnosis·2018

Aneuploidy screening by non-invasive prenatal testing in twin pregnancy.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2016

Nuchal Translucency Quality Review (NTQR) program: first one and half million results.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2014

Measuring total bilirubin for clinical decision making: are we treating at the right number?

Seminars in perinatology·2026

Unbound bilirubin-based management of neonatal hyperbilirubinemia: The Japanese experience and global adaptation.

Seminars in perinatology·2026

Cochlear implantation for sensorineural hearing loss caused by neonatal hyperbilirubinemia.

Seminars in perinatology·2026

Albumin priming prior to an exchange transfusion: Is it time to prime for neuroprotection?

Seminars in perinatology·2026

Advancing the science of Staphylococcus aureus infection prevention in the neonatal intensive care unit.

Seminars in perinatology·2026

The uprise of congenital syphilis in the United States: a preventable failure of perinatal systems.

Seminars in perinatology·2026

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Research (Washington, D.C.)·2026

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Clinical case reports·2026

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Journal of human genetics·2026

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

Nature genetics·2026

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Psychiatric genetics·2026

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Frontiers in genetics·2026

Related Experiment Videos

Genetic factors in intrauterine growth retardation

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Association of human chorionic gonadotropin and post-pregnancy persistent enhanced myometrial vascularity.

United States' experience in nuchal translucency measurement: variation according to provider characteristics in over five million ultrasound examinations.

Accuracy of automated three-dimensional ultrasound imaging technique for fetal head biometry.

Clinical experience of laboratory follow-up with noninvasive prenatal testing using cell-free DNA and positive microdeletion results in 349 cases.

Aneuploidy screening by non-invasive prenatal testing in twin pregnancy.

Nuchal Translucency Quality Review (NTQR) program: first one and half million results.

Measuring total bilirubin for clinical decision making: are we treating at the right number?

Unbound bilirubin-based management of neonatal hyperbilirubinemia: The Japanese experience and global adaptation.

Cochlear implantation for sensorineural hearing loss caused by neonatal hyperbilirubinemia.

Albumin priming prior to an exchange transfusion: Is it time to prime for neuroprotection?

Advancing the science of Staphylococcus aureus infection prevention in the neonatal intensive care unit.

The uprise of congenital syphilis in the United States: a preventable failure of perinatal systems.

Longitudinal Characterization of Giant ANK2-Depleted Monkeys Suggests Neurodevelopmental-Disorder-Like Phenotypes.

Identification of the Genomic Etiology of Unexplained Congenital Problems in Pediatric Patients: First Reported Case With Coffin-Siris Syndrome and Sialuria From India.

Broadening the Okur-Chung syndrome phenotype: adult-onset metabolic features and a contiguous 20p13 deletion in a Turkish multicenter cohort.

Genome-wide association analyses highlight the neuronal contribution to multiple sclerosis susceptibility.

A de novo 1.62 Mb deletion at 2q34 with nonpenetrant neurodevelopmental phenotype at 12 months.

Case Report: novel mutations in SMARCA4 cause Coffin-Siris syndrome type 4 with autism spectrum disorder without visual impairment in one patient.

Related Experiment Videos

Genetic factors in intrauterine growth retardation

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