prenatal diagnosis

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prenatal diagnosis

prenatal diagnosis

Related Articles & Bibliographies

Assessment of uteroplacental vascularisation in early first-trimester pregnancy with contrast-enhanced ultrasound and 3D power Doppler angiography: protocol for a prospective, cross-sectional, multicentre and non-randomised open study ("HOPE Study").

FunDMDeep-m6A: identification and prioritization of functional differential m6A methylation genes.

Dual-frequency CMOS terahertz detector with silicon-based plasmonic antenna.

MRI in the diagnosis of fetal developmental brain abnormalities: the MERIDIAN diagnostic accuracy study.

Impact of Introduction of a Clinical Pathway for the Management of Pyelonephritis on Obstetric Patients: a Quality Improvement Project

Assessment of 6 STR loci for prenatal diagnosis of Duchenne Muscular Dystrophy.

How does carrier status for recessive disorders influence reproductive decisions? A systematic review of the literature.

Zika Virus Detection in Amniotic Fluid and Zika-Associated Birth Defects.

A Patient-Held Smartcard With a Unique Identifier and an mHealth Platform to Improve the Availability of Prenatal Test Results in Rural Nigeria: Demonstration Study

‘essential but not always available when needed’ – an interview study of physicians’ experiences and views regarding use of obstetric ultrasound in tanzania

conhecimento dos obstetras sobre a transmissão vertical da hepatite b knowledge of obstetricians about the vertical transmission of hepatitis b virus

legal ableism, interrupted: developing tort law & policy alternatives to wrongful birth & wrongful life claims

prenatal diagnosis of mos45,x/46,x,+mar in a fetus with normal male external genitalia and a literature review

prenatal diagnosis of congenitally corrected transposition of the great arteries

prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay, and speech delay

molecular genetic characterization of a prenatally detected 1.484-mb xq13.3-q21.1 duplication encompassing atrx and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at xq13.3-q21.1

prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18

detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus from a family with wolf–hirschhorn syndrome

mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: prenatal diagnosis, molecular cytogenetic characterization, and association with 2-mb deletion of 21q21.1–q21.2 and 5-mb deletion of 21q22.3

prenatal hydrocolpos in a male

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