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Journal of Magnetic Resonance (San Diego, Calif. : 1997)
|
September 25, 2004
High-field 19.6T 27Al solid-state MAS NMR of in vitro aluminated brain tissue
Pamela L Bryant, Walter J Lukiw, Zhehong Gan, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2008
Autistic and dysmorphic features associated with a submicroscopic 2q33.3-q34 interstitial deletion detected by array comparative genomic hybridization
Duane T Brandau, Molly Lund, Linda D Cooley, et al.
Genetics Research International
|
November 18, 2014
Clinical Presentation and Microarray Analysis of Peruvian Children with Atypical Development and/or Aberrant Behavior
Merlin G Butler, Kelly Usrey, Jennifer L Roberts, et al.
International Journal of Molecular Sciences
|
March 13, 2024
Mowat-Wilson Syndrome: Case Report and Review of <i>ZEB2</i> Gene Variant Types, Protein Defects and Molecular Interactions
Caroline St Peter, Waheeda A Hossain, Scott Lovell, et al.
Journal of Molecular and Cellular Cardiology
|
August 5, 1998
Dynamic left/right regionalisation of endogenous myosin light chain 3F transcripts in the developing mouse heart
R G Kelly, P S Zammit, V Mouly, et al.
American Journal of Medical Genetics. Part A
|
May 24, 2016
Higher plasma orexin A levels in children with Prader-Willi syndrome compared with healthy unrelated sibling controls
Ann M Manzardo, Lisa Johnson, Jennifer L Miller, et al.
Food Chemistry
|
July 6, 2014
Improving the fatty acid profile of winter milk from housed cows with contrasting feeding regimes by oilseed supplementation
S Stergiadis, C Leifert, C J Seal, et al.
International Journal of Molecular Sciences
|
February 13, 2025
ZEB2 Gene Pathogenic Variants Across Protein-Coding Regions and Impact on Clinical Manifestations: A Review
Waheeda A Hossain, Caroline St Peter, Scott Lovell, et al.
Cellular and Molecular Biology
|
January 1, 1988
Human desmin gene: utilization as a marker of human muscle differentiation
A Lilienbaum, Z Li, G Butler-Browne, et al.
American Journal of Medical Genetics
|
December 1, 1982
Brief clinical report: a child with radius aplasia, cleft of lip and palate, microcephaly, and unusual chromosome findings
M G Butler, L J Russell, C G Palmer, et al.
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Search research articles
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Showing results (671-680 of 1,112) with videos related to
Sort By:
Page
of 112
Journal of Magnetic Resonance (San Diego, Calif. : 1997)
|
September 25, 2004
High-field 19.6T 27Al solid-state MAS NMR of in vitro aluminated brain tissue
Pamela L Bryant, Walter J Lukiw, Zhehong Gan, et al.
American Journal of Medical Genetics. Part A
|
January 19, 2008
Autistic and dysmorphic features associated with a submicroscopic 2q33.3-q34 interstitial deletion detected by array comparative genomic hybridization
Duane T Brandau, Molly Lund, Linda D Cooley, et al.
Genetics Research International
|
November 18, 2014
Clinical Presentation and Microarray Analysis of Peruvian Children with Atypical Development and/or Aberrant Behavior
Merlin G Butler, Kelly Usrey, Jennifer L Roberts, et al.
International Journal of Molecular Sciences
|
March 13, 2024
Mowat-Wilson Syndrome: Case Report and Review of <i>ZEB2</i> Gene Variant Types, Protein Defects and Molecular Interactions
Caroline St Peter, Waheeda A Hossain, Scott Lovell, et al.
Journal of Molecular and Cellular Cardiology
|
August 5, 1998
Dynamic left/right regionalisation of endogenous myosin light chain 3F transcripts in the developing mouse heart
R G Kelly, P S Zammit, V Mouly, et al.
American Journal of Medical Genetics. Part A
|
May 24, 2016
Higher plasma orexin A levels in children with Prader-Willi syndrome compared with healthy unrelated sibling controls
Ann M Manzardo, Lisa Johnson, Jennifer L Miller, et al.
Food Chemistry
|
July 6, 2014
Improving the fatty acid profile of winter milk from housed cows with contrasting feeding regimes by oilseed supplementation
S Stergiadis, C Leifert, C J Seal, et al.
International Journal of Molecular Sciences
|
February 13, 2025
ZEB2 Gene Pathogenic Variants Across Protein-Coding Regions and Impact on Clinical Manifestations: A Review
Waheeda A Hossain, Caroline St Peter, Scott Lovell, et al.
Cellular and Molecular Biology
|
January 1, 1988
Human desmin gene: utilization as a marker of human muscle differentiation
A Lilienbaum, Z Li, G Butler-Browne, et al.
American Journal of Medical Genetics
|
December 1, 1982
Brief clinical report: a child with radius aplasia, cleft of lip and palate, microcephaly, and unusual chromosome findings
M G Butler, L J Russell, C G Palmer, et al.
Page
of 112