ISPD (@ispdhq) 's Twitter Profile
ISPD

@ispdhq

International Society for Prenatal Diagnosis -- Building Global Partnerships in Genetics and Fetal Care

ID: 268433845

linkhttp://www.ispdhome.org calendar_today18-03-2011 19:26:04

1,1K Tweet

4,4K Followers

319 Following

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Prenatal Diagnosis: Maternal Vascular Malperfusion and Anatomic Cord Abnormalities Are Prevalent in Pregnancies With Fetal Congenital Heart Disease dlvr.it/TCbdK3

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Prenatal Diagnosis: The Conundrum of Mechanics Versus Genetics in Congenital Hydrocephalus and Its Implications for Fetal Therapy Approaches: A Scoping Review dlvr.it/TChbQq

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Prenatal Diagnosis: Agenesis of Corpus Callosum, Malformations of Cortical Development, Duodenal Atresia and Fetal Growth Restriction: Prenatal Markers for Zhu‐Tokita‐Takenouchi‐Kim Syndrome dlvr.it/TClD5q

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Prenatal Diagnosis: Prenatal Phenotype of Alkuraya‐Kučinskas Syndrome: A Novel Case and Systematic Literature Review dlvr.it/TCp7bR

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Prenatal Diagnosis: Risk of Genetic Abnormality in Fetuses With Unilateral Versus Bilateral Pleural Effusions dlvr.it/TCv8jy

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Prenatal Diagnosis: Potentially Missed Diagnoses in Prenatal Versus Postnatal Exome Sequencing in the Lack of Informative Phenotype: Lessons Learned From a Postnatal Cohort dlvr.it/TCv8kN

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Prenatal Diagnosis: Reversal of Fetal Compromise Following In Utero Treatment of Vein of Galen Malformation Using Glue dlvr.it/TCz12T

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Prenatal Diagnosis: Imaging‐Based Prediction Parameters of Perinatal Morbidity and Mortality for Fetal Occipital Cephaloceles dlvr.it/TD5MPS

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Prenatal Diagnosis: Maternal Complications After Laser Surgery for Twin‐to‐Twin Transfusion Syndrome, a Cohort Study dlvr.it/TD5MPq

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Prenatal Diagnosis: SNPscan Combined With CNVplex as a High‐Performance Diagnostic Method for Thalassemia dlvr.it/TD5MPr

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Prenatal Diagnosis: Clinical Characteristics and Outcomes of Intrauterine Blood Transfusion (IUT) for Infectious Etiologies dlvr.it/TDD46w

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Prenatal Diagnosis: Correspondence on “Current Controversy in Prenatal Diagnosis: The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use” dlvr.it/TDFs9s

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Prenatal Diagnosis: Response to Wynn and Hokovec Regarding “The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use” dlvr.it/TDFsBq

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Prenatal Diagnosis: Parental or Trio Magnetic Resonance Imaging to Improve Prenatal Counseling in Brain Anomalies dlvr.it/TDVz4R

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Prenatal Diagnosis: Characterization of the Prenatal Ultrasound Phenotype Associated With 7q11.23 Microduplication Syndrome and Williams–Beuren Syndrome dlvr.it/TDVz4d

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Prenatal Diagnosis: Prenatal Sonographic Features of Rubinstein–Taybi Syndrome—A Small Case Series of a Rare Syndrome dlvr.it/TDZ8jb

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Prenatal Diagnosis: Second‐Trimester Ultrasound Receipt Mediates the Relationship Between Public Insurance and Prenatal Diagnosis of a Congenital Heart Defect dlvr.it/TDbmT6

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Prenatal Diagnosis: Prenatal Ultrasonographic Features Associated With ARSL and X‐Linked Chondrodysplasia Punctata 1 (CDPX1): Literature Review and Case Series dlvr.it/TDcPG3