Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay
Burnside, Rachel D., Pasion, Romela, Mikhail, Fady M., Carroll, Andrew J., Robin, Nathaniel H., Youngs, Erin L., Gadi, Inder K., Keitges, Elizabeth, Jaswaney, Vikram L., Papenhausen, Peter R., Potluri, Venkateswara R., Risheg, Hiba, Rush, Brooke, Smith, Janice L., Schwartz, Stuart, Tepperberg, James H., Butler, Merlin G.
Published in Human genetics (01.10.2011)
Published in Human genetics (01.10.2011)
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UPD detection using homozygosity profiling with a SNP genotyping microarray
Papenhausen, Peter, Schwartz, Stuart, Risheg, Hiba, Keitges, Elisabeth, Gadi, Inder, Burnside, Rachel D., Jaswaney, Vikram, Pappas, John, Pasion, Romela, Friedman, Kenneth, Tepperberg, James
Published in American journal of medical genetics. Part A (01.04.2011)
Published in American journal of medical genetics. Part A (01.04.2011)
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Journal Article
The role of the sex-determining region Y gene in the etiology of 46,XX maleness
Fechner, P Y, Marcantonio, S M, Jaswaney, V, Stetten, G, Goodfellow, P N, Migeon, C J, Smith, K D, Berkovitz, G D, Amrhein, J A, Bard, P A
Published in The journal of clinical endocrinology and metabolism (01.03.1993)
Published in The journal of clinical endocrinology and metabolism (01.03.1993)
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Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype
Burnside, Rachel D., Pappas, John G., Sacharow, Stephanie, Applegate, Carolyn, Hamosh, Ada, Gadi, Inder K., Jaswaney, Vikram, Keitges, Elisabeth, Phillips, Karen K., Potluri, Venketaswara R., Risheg, Hiba, Smith, Janice L., Tepperberg, Jim H., Schwartz, Stuart, Papenhausen, Peter
Published in American journal of medical genetics. Part A (01.04.2013)
Published in American journal of medical genetics. Part A (01.04.2013)
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Journal Article
Mosaic trisomy 22: a case presentation and literature review of trisomy 22 phenotypes
Crowe, C A, Schwartz, S, Black, C J, Jaswaney, V
Published in American journal of medical genetics (05.09.1997)
Published in American journal of medical genetics (05.09.1997)
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Journal Article
Three cases of isolated terminal deletion of chromosome 8p without heart defects presenting with a mild phenotype
Burnside, Rachel D., Pappas, John G., Sacharow, Stephanie, Applegate, Carolyn, Hamosh, Ada, Gadi, Inder K., Jaswaney, Vikram, Keitges, Elisabeth, Phillips, Karen K., Potluri, Venketaswara R., Risheg, Hiba, Smith, Janice L., Tepperberg, Jim H., Schwartz, Stuart, Papenhausen, Peter
Published in American Journal of Medical Genetics Part A (01.04.2013)
Published in American Journal of Medical Genetics Part A (01.04.2013)
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Inability to detect fetal metaphases in flow-sorted lymphocyte cultures based on maternal-fetal HLA differences
Tharapel, A T, Jaswaney, V L, Dockter, M E, Wachtel, S S, Chandler, R W, Simpson, J L, Shulman, L P, Meyers, C M, Elias, S
Published in Fetal diagnosis and therapy (01.03.1993)
Published in Fetal diagnosis and therapy (01.03.1993)
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Journal Article
Sex selection with monoclonal H-Y antibody
Wachtel, Stephen, Nakamura, Dean, Wachtel, Gwendolyn, Felton, William, Kent, Marijo, Jaswaney, Vikram
Published in Fertility and sterility (01.08.1988)
Published in Fertility and sterility (01.08.1988)
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Journal Article
Reaction of monoclonal H-Y antibody in the ELISA
Brunner, Michael, Jaswaney, Vikram, Wachtel, Stephen
Published in Journal of reproductive immunology (01.07.1987)
Published in Journal of reproductive immunology (01.07.1987)
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