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Scott D McLean

Showing results (1-10 of 25) with videos related to

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Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 18, 2010
But is the platter really silver?Scott D McLean
British Journal of Haematology|August 4, 2007
Haematopoietic stem cells participate in muscle regenerationMehrdad Abedi, Bethany M Foster, Kyle D Wood, et al.
Optics Express|September 3, 2009
Spectra of particulate backscattering in natural watersHoward R Gordon, Marlon R Lewis, Scott D McLean, et al.
Molecular Cytogenetics|July 15, 2021
Copy neutral absence of heterozygosity on chromosome 15 distal long arm: A surrogate marker for Prader-Willi/Angelman syndromes?Veronica Ortega, Raymond J Louie, Melanie A Jones, et al.
American Journal of Medical Genetics. Part A|December 21, 2022
Patterns of co-occurring birth defects in children with anotia and microtiaJeremy M Schraw, Renata H Benjamin, Charles J Shumate, et al.
American Journal of Medical Genetics. Part A|December 29, 2019
Further delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONOMaham Sewani, Kimberly Nugent, Patrick R Blackburn, et al.
Pediatric Research|July 1, 2021
Birth defect co-occurrence patterns in the Texas Birth Defects RegistryRenata H Benjamin, Angela E Scheuerle, Daryl A Scott, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|April 28, 2021
Birth Defect Co-Occurrence Patterns Among Infants With Cleft Lip and/or PalateMaria Luisa Navarro Sanchez, Renata H Benjamin, Laura E Mitchell, et al.
Birth Defects Research|July 18, 2019
Co-occurring defect analysis: A platform for analyzing birth defect co-occurrence in registriesRenata H Benjamin, Xiao Yu, Maria Luisa Navarro Sanchez, et al.
Molecular Genetics and Metabolism|March 14, 2020
Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiencyMariska Davids, Minal Menezes, Yiran Guo, et al.
Pageof 3

Showing results (1-10 of 25) with videos related to

Sort By:
Pageof 3
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 18, 2010
But is the platter really silver?Scott D McLean
British Journal of Haematology|August 4, 2007
Haematopoietic stem cells participate in muscle regenerationMehrdad Abedi, Bethany M Foster, Kyle D Wood, et al.
Optics Express|September 3, 2009
Spectra of particulate backscattering in natural watersHoward R Gordon, Marlon R Lewis, Scott D McLean, et al.
Molecular Cytogenetics|July 15, 2021
Copy neutral absence of heterozygosity on chromosome 15 distal long arm: A surrogate marker for Prader-Willi/Angelman syndromes?Veronica Ortega, Raymond J Louie, Melanie A Jones, et al.
American Journal of Medical Genetics. Part A|December 21, 2022
Patterns of co-occurring birth defects in children with anotia and microtiaJeremy M Schraw, Renata H Benjamin, Charles J Shumate, et al.
American Journal of Medical Genetics. Part A|December 29, 2019
Further delineation of the phenotypic spectrum associated with hemizygous loss-of-function variants in NONOMaham Sewani, Kimberly Nugent, Patrick R Blackburn, et al.
Pediatric Research|July 1, 2021
Birth defect co-occurrence patterns in the Texas Birth Defects RegistryRenata H Benjamin, Angela E Scheuerle, Daryl A Scott, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association|April 28, 2021
Birth Defect Co-Occurrence Patterns Among Infants With Cleft Lip and/or PalateMaria Luisa Navarro Sanchez, Renata H Benjamin, Laura E Mitchell, et al.
Birth Defects Research|July 18, 2019
Co-occurring defect analysis: A platform for analyzing birth defect co-occurrence in registriesRenata H Benjamin, Xiao Yu, Maria Luisa Navarro Sanchez, et al.
Molecular Genetics and Metabolism|March 14, 2020
Homozygous splice-variants in human ARV1 cause GPI-anchor synthesis deficiencyMariska Davids, Minal Menezes, Yiran Guo, et al.
Pageof 3