Infant with severe penicillamine embryopathy born to a woman with Wilson disease von Pinter, R., Hogge, W.A., McPherson, E.

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First‐trimester trisomy screening: nuchal translucency measurement training and quality assurance to correct and unify technique von Snijders, R. J. M., Thom, E. A., Zachary, J. M., Platt, L. D., Greene, N., Jackson, L. G., Sabbagha, R. E., Filkins, K., Silver, R. K., Hogge, W. A., Ginsberg, N. A., Beverly, S., Morgan, P., Blum, K., Chilis, P., Hill, L. M., Hecker, J., Wapner, R. J.

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Insights into the pathogenesis and natural history of fetuses with multicystic dysplastic kidney disease von Lazebnik, Noam, Bellinger, Mark F., Ferguson, James E., Hogge, Joan S., Hogge, W. Allen

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Technical report: ethical and policy issues in genetic testing and screening of children von Ross, Laine Friedman, Saal, Howard M., David, Karen L., Anderson, Rebecca R.

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Clinical Report-Health Supervision for Children With Prader-Willi Syndrome von MCCANDLESS, Shawn E

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Choroid plexus cysts and trisomy 18: Risk modification based on maternal age and multiple-marker screening von Gratton, Robert J., Hogge, W.Allen, Aston, Christopher E.

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Health supervision for children with Marfan syndrome von Tinkle, Brad T, Saal, Howard M

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X Chromosome Defects as an Etiology of Recurrent Spontaneous Abortion von Lanasa, Mark C., Hogge, W. Allen

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Prenatal diagnosis of cytomegalovirus (CMV) infection: A preliminary report von Hogge, W. Allen, Buffone, Gregory J., Hogge, Joan S.

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A novel X chromosome–linked genetic cause of recurrent spontaneous abortion von Lanasa, Mark C., Hogge, W.Allen, Kubik, Carolyn J., Ness, Roberta B., Harger, James, Nagel, Theodore, Prosen, Tracy, Markovic, Nina, Hoffman, Eric P.

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Chorionic villus sampling: Experience of the first 1000 cases von Hogge, W.A., Schonberg, S.A., Golbus, M.S.

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THE USE OF INTERPHASE FISH FOR PRENATAL DIAGNOSIS OF PALLISTER-KILLIAN SYNDROME von MOWERY-RUSHTON, PATRICIA A., STADLER, MONA P., KOCHMAR, SALLY J., McPHERSON, ELIZABETH, SURTI, URVASHI, ALLEN HOGGE, W.

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Highly Skewed X-Chromosome Inactivation Is Associated with Idiopathic Recurrent Spontaneous Abortion von Lanasa, Mark C., Hogge, W. Allen, Kubik, Carolyn, Blancato, Jan, Hoffman, Eric P.

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Antenatal Diagnosis of Fetal Pelvic Kidneys von HILL, LYNDON M, GRZYBEK, PATRICIA, MILLS, ANNETTE, HOGGE, W ALLEN

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Early Diagnosis of Spina Bifida: The Value of Cranial Ultrasound Markers von THIAGARAJAH, S, HENKE, J, HOGGE, W A, ABBITT, P L, BREEDEN, N, FERGUSON, J E

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Early prenatal diagnosis of an infratentorial arachnoid cyst: Association with an unbalanced translocation von Hogge, W. Allen, Schnatterly, Patricia, Ferguson II, James E.

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Maternal serum screening for fetal trisomy 18: Benefits of patient-specific risk protocol von Hogge, W.Allen, Fraer, Luanne, Melegari, Todd

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Molecular cytogenetics: An essential component of modern prenatal diagnosis von Hogge, W.Allen, Surti, Urvashi, Kochmar, Sally J., Mowery-Rushton, Patricia, Cumbie, Kathleen

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Gorlin syndrome (naevoid basal cell carcinoma syndrome): Prenatal detection in a fetus with macrocephaly and ventriculomegaly von Hogge, W. Allen, Blank, Carol, Roochvarg, Linda B., Hogge, Joan S., Wulfsberg, Eric A., Raffel, Leslie J.

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Congenital nephrosis: Detection of index cases through maternal serum α-fetoprotein screening von Hogge, William A., Hogge, Joan S., Schnatterly, Patricia T., Sun, C.J., Blitzer, Miriam G.

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