Arama Sonuçları - Murry, Jaclyn B.

A genome-wide screen for copy number alterations in an adolescent pilot cohort with Müllerian anomalies Yazar: Murry, Jaclyn B., Santos, Xiomara, Wang, Xiaoling, Wan, Ying-Wooi, Van den Veyver, Ignatia B., Dietrich, Jennifer E.

Tam Metin Erişim Tam Metin Erişim Tam Metin Erişim

Maternal stress in Shank3(ex4-9) mice increases pup-directed care and alters brain white matter in male offspring Yazar: Wong, Bibiana K. Y., Murry, Jaclyn B., Ramakrishnan, Rajesh, He, Fang, Balasa, Alfred, Stinnett, Gary R., Pedersen, Steen E., Pautler, Robia G., Van den Veyver, Ignatia B.

Tam Metin Erişim Tam Metin Erişim Tam Metin Erişim

Interpretation of Genomic Sequencing Results in Healthy and Ill Newborns: Results from the BabySeq Project Yazar: Ceyhan-Birsoy, Ozge, Murry, Jaclyn B., Machini, Kalotina, Lebo, Matthew S., Yu, Timothy W., Fayer, Shawn, Genetti, Casie A., Schwartz, Talia S., Agrawal, Pankaj B., Parad, Richard B., Holm, Ingrid A., McGuire, Amy L., Green, Robert C., Rehm, Heidi L., Beggs, Alan H.

Tam Metin Erişim Tam Metin Erişim Tam Metin Erişim

Reconciling newborn screening and a novel splice variant in BTD associated with partial biotinidase deficiency: a BabySeq Project case report Yazar: Murry, Jaclyn B., Machini, Kalotina, Ceyhan-Birsoy, Ozge, Kritzer, Amy, Krier, Joel B., Lebo, Matthew S., Fayer, Shawn, Genetti, Casie A., VanNoy, Grace E., Yu, Timothy W., Agrawal, Pankaj B., Parad, Richard B., Holm, Ingrid A., McGuire, Amy L., Green, Robert C., Beggs, Alan H., Rehm, Heidi L.

Tam Metin Erişim Tam Metin Erişim Tam Metin Erişim

Expert Specification of the ACMG/AMP Variant Interpretation Guidelines for Genetic Hearing Loss Yazar: Oza, Andrea M., DiStefano, Marina T., Hemphill, Sarah E., Cushman, Brandon J., Grant, Andrew R., Siegert, Rebecca K., Shen, Jun, Chapin, Alex, Boczek, Nicole J., Schimmenti, Lisa A., Murry, Jaclyn B., Hasadsri, Linda, Nara, Kiyomitsu, Kenna, Margaret, Booth, Kevin T., Azaiez, Hela, Griffith, Andrew, Avraham, Karen B., Kremer, Hannie, Rehm, Heidi L., Amr, Sami S., Tayoun, Ahmad N. Abou

Tam Metin Erişim Tam Metin Erişim Tam Metin Erişim

Genotype–phenotype correlations and novel molecular insights into the DHX30-associated neurodevelopmental disorders Yazar: Mannucci, Ilaria, Dang, Nghi D. P., Huber, Hannes, Murry, Jaclyn B., Abramson, Jeff, Althoff, Thorsten, Banka, Siddharth, Baynam, Gareth, Bearden, David, Beleza-Meireles, Ana, Benke, Paul J., Berland, Siren, Bierhals, Tatjana, Bilan, Frederic, Bindoff, Laurence A., Braathen, Geir Julius, Busk, Øyvind L., Chenbhanich, Jirat, Denecke, Jonas, Escobar, Luis F., Estes, Caroline, Fleischer, Julie, Groepper, Daniel, Haaxma, Charlotte A., Hempel, Maja, Holler-Managan, Yolanda, Houge, Gunnar, Jackson, Adam, Kellogg, Laura, Keren, Boris, Kiraly-Borri, Catherine, Kraus, Cornelia, Kubisch, Christian, Le Guyader, Gwenael, Ljungblad, Ulf W., Brenman, Leslie Manace, Martinez-Agosto, Julian A., Might, Matthew, Miller, David T., Minks, Kelly Q., Moghaddam, Billur, Nava, Caroline, Nelson, Stanley F., Parant, John M., Prescott, Trine, Rajabi, Farrah, Randrianaivo, Hanitra, Reiter, Simone F., Schuurs-Hoeijmakers, Janneke, Shieh, Perry B., Slavotinek, Anne, Smithson, Sarah, Stegmann, Alexander P. A., Tomczak, Kinga, Tveten, Kristian, Wang, Jun, Whitlock, Jordan H., Zweier, Christiane, McWalter, Kirsty, Juusola, Jane, Quintero-Rivera, Fabiola, Fischer, Utz, Yeo, Nan Cher, Kreienkamp, Hans-Jürgen, Lessel, Davor

Tam Metin Erişim Tam Metin Erişim Tam Metin Erişim