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V Reid Sutton

Showing results (81-90 of 184) with videos related to

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Frontiers in Genetics|July 16, 2024
Succinic semialdehyde dehydrogenase deficiency: a metabolic and genomic approach to diagnosisKevin E Glinton, Charul Gijavanekar, Abbhirami Rajagopal, et al.
Clinical Genetics|February 13, 2021
Health-related quality of life in adults with osteogenesis imperfectaChaya N Murali, Brady Slater, Salma Musaad, et al.
Human Genetics|August 26, 2003
Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12)V Reid Sutton, William H McAlister, Terry K Bertin, et al.
Pediatric Endocrinology Reviews : PER|June 28, 2019
Hormones and their Structural and Functional Effects on the Brain: How Can We Change our Practice Moving Forward?Bonnie McCann-Crosby, Laurel Hyle, David Mann, et al.
Molecular Genetics and Metabolism|April 17, 2017
Elucidation of the complex metabolic profile of cerebrospinal fluid using an untargeted biochemical profiling assayAdam D Kennedy, Kirk L Pappan, Taraka R Donti, et al.
Advances in Pediatrics|December 9, 2009
The gender medicine team: "it takes a village"Marni E Axelrad, Jonathan S Berg, Leslie Ayensu Coker, et al.
Nature Genetics|June 5, 2007
Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasiaXiaoling Wang, V Reid Sutton, J Omar Peraza-Llanes, et al.
JBMR Plus|October 5, 2018
Whole-Exome Sequencing Identifies an Intronic Cryptic Splice Site in <i>SERPINF1</i> Causing Osteogenesis Imperfecta Type VIZixue Jin, Lindsay C Burrage, Ming-Ming Jiang, et al.
Pediatric Endocrinology Reviews : PER|July 18, 2015
Androgen Insensitivity Syndrome: Management Considerations from Infancy to AdulthoodMin-Jye Chen, Bach-Mai K Vu, Marni Axelrad, et al.
International Journal of Pediatric Endocrinology|April 16, 2014
State of the art review in gonadal dysgenesis: challenges in diagnosis and managementBonnie McCann-Crosby, Roshanak Mansouri, Jennifer E Dietrich, et al.
Pageof 19

Showing results (81-90 of 184) with videos related to

Sort By:
Pageof 19
Frontiers in Genetics|July 16, 2024
Succinic semialdehyde dehydrogenase deficiency: a metabolic and genomic approach to diagnosisKevin E Glinton, Charul Gijavanekar, Abbhirami Rajagopal, et al.
Clinical Genetics|February 13, 2021
Health-related quality of life in adults with osteogenesis imperfectaChaya N Murali, Brady Slater, Salma Musaad, et al.
Human Genetics|August 26, 2003
Skeletal defects in paternal uniparental disomy for chromosome 14 are re-capitulated in the mouse model (paternal uniparental disomy 12)V Reid Sutton, William H McAlister, Terry K Bertin, et al.
Pediatric Endocrinology Reviews : PER|June 28, 2019
Hormones and their Structural and Functional Effects on the Brain: How Can We Change our Practice Moving Forward?Bonnie McCann-Crosby, Laurel Hyle, David Mann, et al.
Molecular Genetics and Metabolism|April 17, 2017
Elucidation of the complex metabolic profile of cerebrospinal fluid using an untargeted biochemical profiling assayAdam D Kennedy, Kirk L Pappan, Taraka R Donti, et al.
Advances in Pediatrics|December 9, 2009
The gender medicine team: "it takes a village"Marni E Axelrad, Jonathan S Berg, Leslie Ayensu Coker, et al.
Nature Genetics|June 5, 2007
Mutations in X-linked PORCN, a putative regulator of Wnt signaling, cause focal dermal hypoplasiaXiaoling Wang, V Reid Sutton, J Omar Peraza-Llanes, et al.
JBMR Plus|October 5, 2018
Whole-Exome Sequencing Identifies an Intronic Cryptic Splice Site in <i>SERPINF1</i> Causing Osteogenesis Imperfecta Type VIZixue Jin, Lindsay C Burrage, Ming-Ming Jiang, et al.
Pediatric Endocrinology Reviews : PER|July 18, 2015
Androgen Insensitivity Syndrome: Management Considerations from Infancy to AdulthoodMin-Jye Chen, Bach-Mai K Vu, Marni Axelrad, et al.
International Journal of Pediatric Endocrinology|April 16, 2014
State of the art review in gonadal dysgenesis: challenges in diagnosis and managementBonnie McCann-Crosby, Roshanak Mansouri, Jennifer E Dietrich, et al.
Pageof 19