Genetic modifiers of abnormal organelle biogenesis in a Drosophila model of BLOC-1 deficiency
Cheli, Verónica T., Daniels, Richard W., Godoy, Ruth, Hoyle, Diego J., Kandachar, Vasundhara, Starcevic, Marta, Martinez-Agosto, Julian A., Poole, Stephen, DiAntonio, Aaron, Lloyd, Vett K., Chang, Henry C., Krantz, David E., Dell'Angelica, Esteban C.
Published in Human molecular genetics (01.03.2010)
Published in Human molecular genetics (01.03.2010)
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The white Gene of Drosophila melanogaster Encodes a Protein with a Role in Courtship Behavior
Anaka, Matthew, Macdonald, C. Danielle, Barkova, Eva, Simon, Karl, Rostom, Reem, Godoy, Ruth A., Haigh, Andrew J., Meinertzhagen, Ian A., Lloyd, Vett
Published in Journal of neurogenetics (01.01.2008)
Published in Journal of neurogenetics (01.01.2008)
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Exome and genome sequencing in adults with undiagnosed disease: a prospective cohort study
Shickh, Salma, Gutierrez Salazar, Mariana, Zakoor, Kathleen-Rose, Lázaro, Conxi, Gu, Jessica, Goltz, Jamie, Kleinman, Dakota, Noor, Abdul, Khalouei, Sam, Mighton, Chloe, Reble, Emma, Kodida, Rita, Bombard, Yvonne, DiTroia, Stephanie, Baxter, Samantha, Watkins, Nicholas, Care, Melanie, Adler, Arnon, Horsburgh, Sheri, Morar, Oana, Murphy, Jillian, Nevay, Dayna-Lynn, Szybowska, Marta, Aronson, Melyssa, Panchal, Seema, Godoy, Ruth, Holter, Spring, Randall Armel, Susan, Semotiuk, Kara, Elser, Christine, Kim, Raymond H, Chitayat, David, So, Joyce, Faghfoury, Hanna, Silver, Josh, Morel, Chantal F, Lerner-Ellis, Jordan
Published in Journal of medical genetics (01.04.2021)
Published in Journal of medical genetics (01.04.2021)
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Homozygous GLUL deletion is embryonically viable and leads to glutamine synthetase deficiency
Roifman, Maian, Niles, Kirsten M., MacNeil, Lauren, Blaser, Susan, Noor, Abdul, Godoy, Ruth, Mieghem, Tim, Ryan, Greg, Seaward, Gareth, Sondheimer, Neal, Mercimek‐Andrews, Saadet, Schulze, Andreas, Hewson, Stacy, Ovadia, Adi, Chitayat, David, Morgen, Eric K., Hojilla, Carlo, Kolomietz, Elena, Watkins, Nicholas, Häberle, Johannes, Shannon, Patrick
Published in Clinical genetics (01.12.2020)
Published in Clinical genetics (01.12.2020)
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Warsaw breakage syndrome: Further clinical and genetic delineation
Alkhunaizi, Ebba, Shaheen, Ranad, Bharti, Sanjay Kumar, Joseph‐George, Ann M., Chong, Karen, Abdel‐Salam, Ghada M. H., Alowain, Mohammed, Blaser, Susan I., Papsin, Blake C., Butt, Mohammed, Hashem, Mais, Martin, Nicole, Godoy, Ruth, Brosh, Robert M., Alkuraya, Fowzan S., Chitayat, David
Published in American journal of medical genetics. Part A (01.11.2018)
Published in American journal of medical genetics. Part A (01.11.2018)
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Uso de herramientas tecnológicas para la resolución de problemas en el área de las matemáticas
Bejarano Cordoba, Andrés Samir, Guerrero Godoy, Ruth Stella
Published in Educare (Caracas) (21.12.2021)
Published in Educare (Caracas) (21.12.2021)
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1.- Uso de herramientas tecnológicas para la resolución de problemas en el área de las matemáticas
Andrés Samir Bejarano Cordoba, Ruth Stella Guerrero Godoy
Published in Educare (Caracas) (01.12.2021)
Published in Educare (Caracas) (01.12.2021)
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