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American Journal of Medical Genetics. Part A
|
March 29, 2014
Clinical evidence for a mandibular to maxillary transformation in Auriculocondylar syndrome
Christopher T Gordon, Christopher M Cunniff, Glenn E Green, et al.
American Journal of Medical Genetics. Part A
|
November 24, 2017
Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms
Christine M Clarke, Vincent T Fok, Jennifer A Gustafson, et al.
Carcinogenesis
|
May 3, 2003
Changes in global gene and protein expression during early mouse liver carcinogenesis induced by non-genotoxic model carcinogens oxazepam and Wyeth-14,643
Mari Iida, Colleen H Anna, Jennifer Hartis, et al.
American Journal of Medical Genetics. Part A
|
March 9, 2007
Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations
Marianne L Seto, Anne V Hing, Jocelyn Chang, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
April 16, 2004
Gene expression profiling of rat livers reveals indicators of potential adverse effects
Alexandra N Heinloth, Richard D Irwin, Gary A Boorman, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
August 19, 2011
Parameters of care for craniosynostosis
Joseph G McCarthy, Stephen M Warren, Joseph Bernstein, et al.
Environmental Health Perspectives
|
May 4, 2004
Human consumption of methyleugenol and its elimination from serum
Arnold Schecter, George W Lucier, Michael L Cunningham, et al.
Journal of Medical Genetics
|
January 13, 2021
Unexpected role of <i>SIX1</i> variants in craniosynostosis: expanding the phenotype of <i>SIX1</i>-related disorders
Eduardo Calpena, Maud Wurmser, Simon J McGowan, et al.
American Journal of Medical Genetics. Part A
|
February 19, 2015
Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders
Elizabeth J Leslie, James O'Sullivan, Michael L Cunningham, et al.
Scientific Reports
|
April 12, 2024
Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428
Anthony M Musolf, Cristina M Justice, Zeynep Erdogan-Yildirim, et al.
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of 17
Search research articles
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Showing results (131-140 of 162) with videos related to
Sort By:
Page
of 17
American Journal of Medical Genetics. Part A
|
March 29, 2014
Clinical evidence for a mandibular to maxillary transformation in Auriculocondylar syndrome
Christopher T Gordon, Christopher M Cunniff, Glenn E Green, et al.
American Journal of Medical Genetics. Part A
|
November 24, 2017
Single suture craniosynostosis: Identification of rare variants in genes associated with syndromic forms
Christine M Clarke, Vincent T Fok, Jennifer A Gustafson, et al.
Carcinogenesis
|
May 3, 2003
Changes in global gene and protein expression during early mouse liver carcinogenesis induced by non-genotoxic model carcinogens oxazepam and Wyeth-14,643
Mari Iida, Colleen H Anna, Jennifer Hartis, et al.
American Journal of Medical Genetics. Part A
|
March 9, 2007
Isolated sagittal and coronal craniosynostosis associated with TWIST box mutations
Marianne L Seto, Anne V Hing, Jocelyn Chang, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
April 16, 2004
Gene expression profiling of rat livers reveals indicators of potential adverse effects
Alexandra N Heinloth, Richard D Irwin, Gary A Boorman, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
August 19, 2011
Parameters of care for craniosynostosis
Joseph G McCarthy, Stephen M Warren, Joseph Bernstein, et al.
Environmental Health Perspectives
|
May 4, 2004
Human consumption of methyleugenol and its elimination from serum
Arnold Schecter, George W Lucier, Michael L Cunningham, et al.
Journal of Medical Genetics
|
January 13, 2021
Unexpected role of <i>SIX1</i> variants in craniosynostosis: expanding the phenotype of <i>SIX1</i>-related disorders
Eduardo Calpena, Maud Wurmser, Simon J McGowan, et al.
American Journal of Medical Genetics. Part A
|
February 19, 2015
Expanding the genetic and phenotypic spectrum of popliteal pterygium disorders
Elizabeth J Leslie, James O'Sullivan, Michael L Cunningham, et al.
Scientific Reports
|
April 12, 2024
Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428
Anthony M Musolf, Cristina M Justice, Zeynep Erdogan-Yildirim, et al.
Page
of 17