Search research articles
Contact Us
Filters
Showing results (651-660 of 687) with videos related to
Page
of 69
Sort By:
The Journal of Clinical Endocrinology and Metabolism
|
December 14, 2011
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency
Nils Krone, Nicole Reisch, Jan Idkowiak, et al.
Nature Genetics
|
February 1, 2017
Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts
Emma M Jenkinson, Mathieu P Rodero, Paul R Kasher, et al.
Nature Genetics
|
August 30, 2016
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts
Emma M Jenkinson, Mathieu P Rodero, Paul R Kasher, et al.
American Journal of Human Genetics
|
June 5, 2018
De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder
Margot R F Reijnders, Kerry A Miller, Mohsan Alvi, et al.
American Journal of Human Genetics
|
September 12, 2007
Clinical and molecular phenotype of Aicardi-Goutieres syndrome
Gillian Rice, Teresa Patrick, Rekha Parmar, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
Science (New York, N.Y.)
|
June 18, 2021
Approaching the motional ground state of a 10-kg object
Chris Whittle, Evan D Hall, Sheila Dwyer, et al.
Physical Review Letters
|
December 24, 2021
Point Absorber Limits to Future Gravitational-Wave Detectors
Wenxuan Jia, Hiroaki Yamamoto, Kevin Kuns, et al.
Applied Optics
|
May 13, 2021
Point absorbers in Advanced LIGO
Aidan F Brooks, Gabriele Vajente, Hiro Yamamoto, et al.
Physical Review Letters
|
December 24, 2019
Quantum-Enhanced Advanced LIGO Detectors in the Era of Gravitational-Wave Astronomy
M Tse, Haocun Yu, N Kijbunchoo, et al.
Page
of 69
Search research articles
Search
Showing results (651-660 of 687) with videos related to
Sort By:
Page
of 69
The Journal of Clinical Endocrinology and Metabolism
|
December 14, 2011
Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency
Nils Krone, Nicole Reisch, Jan Idkowiak, et al.
Nature Genetics
|
February 1, 2017
Corrigendum: Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts
Emma M Jenkinson, Mathieu P Rodero, Paul R Kasher, et al.
Nature Genetics
|
August 30, 2016
Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts
Emma M Jenkinson, Mathieu P Rodero, Paul R Kasher, et al.
American Journal of Human Genetics
|
June 5, 2018
De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder
Margot R F Reijnders, Kerry A Miller, Mohsan Alvi, et al.
American Journal of Human Genetics
|
September 12, 2007
Clinical and molecular phenotype of Aicardi-Goutieres syndrome
Gillian Rice, Teresa Patrick, Rekha Parmar, et al.
American Journal of Medical Genetics. Part A
|
January 22, 2015
Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
Yanick J Crow, Diana S Chase, Johanna Lowenstein Schmidt, et al.
Science (New York, N.Y.)
|
June 18, 2021
Approaching the motional ground state of a 10-kg object
Chris Whittle, Evan D Hall, Sheila Dwyer, et al.
Physical Review Letters
|
December 24, 2021
Point Absorber Limits to Future Gravitational-Wave Detectors
Wenxuan Jia, Hiroaki Yamamoto, Kevin Kuns, et al.
Applied Optics
|
May 13, 2021
Point absorbers in Advanced LIGO
Aidan F Brooks, Gabriele Vajente, Hiro Yamamoto, et al.
Physical Review Letters
|
December 24, 2019
Quantum-Enhanced Advanced LIGO Detectors in the Era of Gravitational-Wave Astronomy
M Tse, Haocun Yu, N Kijbunchoo, et al.
Page
of 69