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R Roeder

Showing results (21-30 of 57) with videos related to

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Nature Genetics|October 15, 1998
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-pairedS A Brown, D Warburton, L Y Brown, et al.
American Journal of Medical Genetics|April 15, 2000
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndromeA E Lin, E V Semina, S Daack-Hirsch, et al.
Journal of Dentistry|July 27, 2023
High-viscosity glass-ionomer cement or composite resin for restorations in posterior permanent teeth? A systematic review and meta-analysesLisiane Cribari, Luciano Madeira, Renata B R Roeder, et al.
Journal of Medical Genetics|October 6, 2010
Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond--Blackfan anaemiaMargaret J Wat, Victoria B Enciso, Wojciech Wiszniewski, et al.
Iscience|January 17, 2024
Plumage microorganism communities of tidal marsh sparrowsAlice M Hotopp, Brian J Olsen, Suzanne L Ishaq, et al.
Oncogene|May 6, 1998
Genomics and transcription analysis of human TFIIDM Purrello, C Di Pietro, A Viola, et al.
Oncogene|August 25, 2001
Genes for human general transcription initiation factors TFIIIB, TFIIIB-associated proteins, TFIIIC2 and PTF/SNAPC: functional and positional candidates for tumour predisposition or inherited genetic diseases?M Purrello, C Di Pietro, A Rapisarda, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 29, 2003
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like featuresErich Roessler, Yang-Zhu Du, Jose L Mullor, et al.
Ecotoxicology (London, England)|August 12, 2021
Geographic variation of mercury in breeding tidal marsh sparrows of the northeastern United StatesChristopher J Sayers, Mackenzie R Roeder, Lindsay M Forrette, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
Reproductive fitness in maternal homocystinuria due to cystathionine beta-synthase deficiencyH L Levy, J E Vargas, S E Waisbren, et al.
Pageof 6

Showing results (21-30 of 57) with videos related to

Sort By:
Pageof 6
Nature Genetics|October 15, 1998
Holoprosencephaly due to mutations in ZIC2, a homologue of Drosophila odd-pairedS A Brown, D Warburton, L Y Brown, et al.
American Journal of Medical Genetics|April 15, 2000
Exclusion of the branchio-oto-renal syndrome locus (EYA1) from patients with branchio-oculo-facial syndromeA E Lin, E V Semina, S Daack-Hirsch, et al.
Journal of Dentistry|July 27, 2023
High-viscosity glass-ionomer cement or composite resin for restorations in posterior permanent teeth? A systematic review and meta-analysesLisiane Cribari, Luciano Madeira, Renata B R Roeder, et al.
Journal of Medical Genetics|October 6, 2010
Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly Diamond--Blackfan anaemiaMargaret J Wat, Victoria B Enciso, Wojciech Wiszniewski, et al.
Iscience|January 17, 2024
Plumage microorganism communities of tidal marsh sparrowsAlice M Hotopp, Brian J Olsen, Suzanne L Ishaq, et al.
Oncogene|May 6, 1998
Genomics and transcription analysis of human TFIIDM Purrello, C Di Pietro, A Viola, et al.
Oncogene|August 25, 2001
Genes for human general transcription initiation factors TFIIIB, TFIIIB-associated proteins, TFIIIC2 and PTF/SNAPC: functional and positional candidates for tumour predisposition or inherited genetic diseases?M Purrello, C Di Pietro, A Rapisarda, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 29, 2003
Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like featuresErich Roessler, Yang-Zhu Du, Jose L Mullor, et al.
Ecotoxicology (London, England)|August 12, 2021
Geographic variation of mercury in breeding tidal marsh sparrows of the northeastern United StatesChristopher J Sayers, Mackenzie R Roeder, Lindsay M Forrette, et al.
Journal of Inherited Metabolic Disease|September 14, 2002
Reproductive fitness in maternal homocystinuria due to cystathionine beta-synthase deficiencyH L Levy, J E Vargas, S E Waisbren, et al.
Pageof 6