High throughput fluorescence-based conformation-sensitive gel electrophoresis (F-CSGE) identifies six unique BRCA2 mutations and an overall low incidence of BRCA2 mutations in high... von GANGULY, T, DHULIPALA, R, GODMILOW, L, GANGULY, A

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Duty to re-contact von Hirschhorn, K, Fleisher, L D, Godmilow, L, Howell, R R, Lebel, R R, McCabe, E R, McGinniss, M J, Milunsky, A, Pelias, M Z, Pyeritz, R E, Sujansky, E, Thompson, B H, Zinberg, R E

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Sensitive multistep clinical molecular screening of 180 unrelated individuals with retinoblastoma detects 36 novel mutations in the RB1 gene von Nichols, Kim E., Houseknecht, Monisa D., Godmilow, Lynn, Bunin, Greta, Shields, Carol, Meadows, Anna, Ganguly, Arupa

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Exon skipping caused by an intronic insertion of a young Alu Yb9 element leads to severe hemophilia A von GANGULY, Arupa, DUNBAR, Tanya, CHEN, Peiqin, GODMILOW, Lynn, GANGULY, Tapan

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Significance of sonographically detected second‐trimester choroid plexus cysts: a series of 211 cases and a review of the literature von Nava, S., Godmilow, L., Reeser, S., Ludomirsky, A., Donnenfeld, A. E.

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Professional Disclosure of Familial Genetic Information von The American Society of Human Genetics Social Issues Subcommittee on Familial Disclosure

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High throughput mutation screening of the factor VIII gene (F8C) in hemophilia A: 37 novel mutations and genotype-phenotype correlation von Citron, Michael, Godmilow, Lynn, Ganguly, Tapan, Ganguly, Arupa

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Genetic Amniocentesis at 14 Weeks or Less von Johnson, Anthony, Godmilow, Lynn

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Significance of Sonographically Detected Second-Trimester Choroid Plexus Cysts: A Series of 211 Cases and a Review of the Literature von Nava, S, Godmilow, L, Reeser, S, Ludomirsky, A, Donnenfeld, A. E

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Commercialization of BRCA1/2 testing: Practitioner awareness and use of a new genetic test von Cho, M.K., Sankar, P., Wolpe, P.R., Godmilow, L.

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Genetic testing of children at risk for Huntington's disease von NANCE, M. A

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Prenatal Genetic Diagnosis in a Triplet Gestation von Hausknecht, R U, Yeh, H C, Godmilow, L

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Ultrasound-adjusted risk and spectrum of fetal chromosomal abnormality in women with elevated maternal serum alpha-fetoprotein von Megerian, Garo, Godmilow, Lynn, Donnenfeld, Alan E.

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Acute hemodynamic effects induced by chorionic villus sampling: A preliminary investigation von Zoppini, Cinzia, Ludomirsky, Avi, Godmilow, Lynn, Weiner, Stuart, Maislin, Greg, Donnenfeld, Alan E.

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Prenatal diagnosis of Fraser syndrome at 18.5 weeks gestation, with autopsy findings at 19 weeks von Schauer, G. M., Dunn, L. K., Godmilow, L., Eagle Jr, R. C., Knisely, A. S.

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Chorionic villus sampling followed by amniocentesis in the same pregnancy von Donnenfeld, Alan E., Librizzi, Ronald J., Dunn, Linda K., Craparo, Frank, Godmilow, Lynn, Weiner, Stuart

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Chorionic villus sampling utilization following reports of a possible association with fetal limb defects von Cutillo, Denise M., Hammond, Elizabeth A., Reeser, Suzanne L., Kershner, Melissa A., Lukin, Barbara, Godmilow, Lynn, Donnenfeld, Alan E.

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Prenatal diagnosis of renal anomalies von Kaffe, Sara, Rose, Judith S., Godmilow, Lynn, Walker, Barbara A., Kerenyi, Thomas, Beratis, Nicholas, Reyes, Pilar, Hirschhorn, Kurt, Karp, L. E.

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Prenatal cytogenetic diagnosis: First 1,000 successful cases von Hsu, Lillian Y. F., Kaffe, Sara, Yahr, Felice, Serotkin, Andrea, Giordano, Frances, Godmilow, Lynn, Kim, Hyon J., David, Karen, Kerenyi, Thomas, Hirschhorn, Kurt, Opitz, John M.

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Caucasian family with two independent mutations: 2594delC in BRCA1 and 5392delAG in BRCA2 gene von Ganguly, Arupa, Citron, Michael, Godmilow, Lynn, Ahrens, Mary, Ganguly, Tapan

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