Journal of Fetal Medicine

Issue 01 · Volume 10 · April 2023 DOI: 10.1055/s-013-57776

Research Article

001

Jakkidi, Anusha; Singh, Arati; Redishetty, Saritha; Kavuri, Kamala; Reddy, Prathibha; Shah, Aditi; Kachakayala, Mounika; Kolar, Geeta; Vavilala, Suseela: Comparative Study of Perinatal Outcome in Uncomplicated Monochorionic Diamniotic versus Dichorionic Diamniotic Twins at a Specialized Twin Clinic—A Prospective Study

009

Khatter, Sangeeta; Lall, Meena; Agrawal, Shruti; Mahay, Sunita Bijarnia; Dimri, Nandita; Sharma, Nidhish; Gujral, Kanwal; Verma, Ishwar C.; Puri, Ratna D.: The Impact of Isolated Increased Nuchal Translucency ≥95th Centile on Perinatal Outcome: A Prospective Cohort Study from a North Indian Genetic Center

016

Natarajan, Sumathi; Alavandar, Ezhilmathi; Kashyap, Ravindar; Rajan, Saira; Muthusamy, Dhivakar; Subramani, Amuthavalli: Correlation of Cervical Length, Anterior Uterocervical Angle, and Cervical Elastography with the Incidence of Preterm Labor

023

Thakur, Seema; Singh, Chanchal; Paliwal, Preeti; Shahnaaz, Ghazala; Dagar, Savita; Mallik, Manish; Jain, Puneet; Sethia, Vineet: Practical Applications of Chromosomal Microarray in Prenatal Diagnosis

029

Mangla, Mishu; Sree, Kottu Divya Satya; Kumar, Naina; Panda, Meely: Knowledge and Attitude of Young Married Women Regarding Congenital Anomalies in the Fetus: A Cross-Sectional Questionnaire-Based Study from South-Central India

Case Report

036

Kane, Daniel T.; Dempsey, Mark A.; Burke, Annette L.; Morrison, John J.: Prenatal Diagnosis and Fetal Sonographic Features of Swyer Syndrome

040

Verma, Heena; Patel, B I.; Patel, Nisha S.; Patel, Saumil B.: Enlarged Intracranial Translucency, as a Potential Marker for Diagnosis of Joubert Syndrome during First-Trimester Screening: A Case Report

046

Lallar, Meenakshi; Kaur, Ladbans; Preet, Meetan; Singh, U. P.: Congenital Cataract and Narrow CSP: A Clue to Prenatal Diagnosis of RAB3GAP1-Associated Warburg Micro Syndrome

049

Murarka, Shiva; Kotecha, Udhaya; Pamnani, Dirgha; Shah, Parth; Sharda, Sheetal: A Rare Case of Microduplication on Chromosome 13 Detected as High Risk for Trisomy 13 on NIPT Screening