Erica Schindewolf

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Prenatal cardiac findings and 22q11.2 deletion syndrome: Fetal detection and evaluation.

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Enlarged cavum septum pellucidum and small thymus as markers for 22q11.2 deletion syndrome.

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The importance of patient-specific resources for families dealing with prenatal rare diseases

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Prenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age.

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Age-related differences in the presentation of COL4A1/2-related disorders

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Importance of Prenatal Evaluation in 22q11.2 Deletion syndrome

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Diagnosis of Au Kline Syndrome in a Fetus with Lower Urinary Tract Obstruction: A Case Report and Literature Review

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Fetus with Cole-Carpenter Type 2 Presenting with Novel Neonatal Lethal Skeletal Dysplasia.

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Genetics of Prenatally Diagnosed Micro/Anopthalmia

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Milroy Disease Presenting as Hydrops Fetalis: A Case Series.

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Two Fetuses with Hereditary Hemorrhaghic Telangiectasia Presenting with Rare Finding of Arteriovenous Malformation.

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Utility of Genetic Evaluation of Congenital Posterior Fossa Anomalies. Granted Top Abstract Award.

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Course Director Reproductive Genetics