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Seite 1 für „prenatal“ · Literaturverweise aus öffentlichen Artikeln
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Non-Invasive Prenatal Testing (NIPT): Reliability, Challenges, and Future Directions
pubmed · 37568933
Literaturverweis öffnenPrenatal Diagnosis of Cartilage-Hair Hypoplasia: A Narrative Review
pubmed · 41525162
Literaturverweis öffnenIndication and diagnostic method selection for invasive prenatal genetic testing – review of the literature and conclusions of the Austrian consensus conference on prenatal genetic testing
pubmed · 42022385
Literaturverweis öffnenPrenatal ultrasound diagnosis of intrauterine caput succedaneum: Case report
pubmed · 40960127
Literaturverweis öffnenPrenatal, Perinatal, and Familial Risk Factors in the Differential Diagnosis Between Autism Spectrum Disorder and Phenylketonuria: A Retrospective Case-Control Study in the Absence of Neonatal Screening
pubmed · 42496180
Literaturverweis öffnenThe Relationship Between Prenatal Visits and Age of Hip Dysplasia Diagnosis in Infants
doi · 10.22541/au.171772785.54767085/v1
Literaturverweis öffnenBlended Phenotype Involving FBN1 and Novel PIGL Variants of Uncertain Significance: A Prenatal Case Report
pubmed · 42377900
Literaturverweis öffnenSevere Recurrent Polyhydramnios as a Prenatal Signal of MAGED2-Related Bartter Syndrome: A Clinical Perspective
pubmed · 42079331
Literaturverweis öffnenPrenatal Diagnosis of a Fetus With Congenital Malformations Caused by Compound Heterozygous Mutations in FANCA: A Case Report and Literature Review
pubmed · 42432871
Literaturverweis öffnen[Single umbilical artery--consequences of prenatal diagnosis].
pubmed · 1595307
Literaturverweis öffnenPrenatal-Onset Lethal Adenylosuccinate Lyase Deficiency Diagnosed by Rapid Whole Genome Sequencing: A Case Report
pubmed · 42338846
Literaturverweis öffnenThe added value of whole-exome sequencing for fetuses with postural defects by prenatal ultrasound
pubmed · 42423164
Literaturverweis öffnenDiscrepant findings of prenatal diagnostics in a case of fetal partial trisomy 21 and fetoplacental mosaicism
pubmed · 41965835
Literaturverweis öffnenPrenatal diagnosis, genetic analysis, and pregnancy outcomes of fetuses with mosaic isodicentric Y chromosomes
pubmed · 42046074
Literaturverweis öffnenMaternal Prenatal Psychosocial Stress in Relation to Maternal and Neonatal Anemia
pubmed · 41732741
Literaturverweis öffnenRecommendations of the AGG (Obstetrics and Prenatal Medicine Working Group, Section Maternal Diseases) on Maternal Thrombocytopenia in Pregnancy
pubmed · 41089217
Literaturverweis öffnenPrenatal Diagnosis of Renal Cysts and Diabetes Syndrome (RCAD): A Case Report
pubmed · 41999034
Literaturverweis öffnenShock in Pregnancy – Recommendations of the German Interdisciplinary Association for Intensive and Emergency Medicine (DIVI – Section Shock) and the Working Group on Obstetrics and Prenatal Medicine (AGG – Section on Maternal Disorders)
pubmed · 41347061
Literaturverweis öffnenPrenatal Diagnosis of Craniorachischisis Totalis Following an Initially Normal First-Trimester Ultrasound in a Woman With Two Previous Caesarean Births: A Case Report
pubmed · 42438610
Literaturverweis öffnenChromosomal abnormalities and pregnancy outcomes in 350 pregnancies with prenatally diagnosed aberrant right subclavian artery: a phenotype-based retrospective cohort study
pubmed · 42219360
Literaturverweis öffnenEffects of Prenatal Electronic Cigarette Exposure On Foetal Development: a Review of the Literature
pubmed · 34754272
Literaturverweis öffnenIdentification of Complex Chromosomal Rearrangement Involving Chromosomes 10, 18, and 19 in a Family Undergoing Prenatal Diagnosis: Case Report
pubmed · 42382047
Literaturverweis öffnenPrenatal Diagnosis and Monitoring of Type III Congenital Pulmonary Airway Malformation: A Case Report
pubmed · 42338819
Literaturverweis öffnenIn Situ Simulation in Prenatal Breastfeeding Education: A Pilot Study
pubmed · 42093526
Literaturverweis öffnenRole of Ultrasound and Fetal MRI in the Prenatal Assessment of Congenital Cytomegalovirus Infection: A Systematic Review
pubmed · 42194606
Literaturverweis öffnenPrenatal initiation of elexacaftor/tezacaftor/ivacaftor via carrier mother prevents congenital bilateral absence of vas deferens in a male infant with cystic fibrosis
pubmed · 41654435
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