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A Schrier

Showing results (31-40 of 71) with videos related to

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The British Journal of Ophthalmology|May 1, 1996
Infectious keratitis with corneal perforation associated with corneal hydrops and contact lens wear in keratoconusE D Donnenfeld, A Schrier, H D Perry, et al.
American Journal of Medical Genetics. Part A|March 5, 2015
Mosaic trisomy 15 in a liveborn infantJacob McPadden, Benjamin M Helm, Brooke B Spangler, et al.
American Journal of Medical Genetics. Part A|July 7, 2022
Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic herniaYoel Gofin, Xiaonan Zhao, Amanda Gerard, et al.
American Journal of Medical Genetics. Part A|December 9, 2021
Further supporting SMARCC2-related neurodevelopmental disorder through exome analysis and reanalysis in two patientsDong Li, Helen Downes, Cuiping Hou, et al.
American Journal of Medical Genetics. Part A|September 5, 2015
Beyond Ohdo syndrome: A familial missense mutation broadens the MED12 spectrumKatherine G Langley, Jordan Brown, Richard J Gerber, et al.
Pharmaceutical Research|July 1, 1993
Degradation pathways for recombinant human macrophage colony-stimulating factor in aqueous solutionJ A Schrier, R A Kenley, R Williams, et al.
American Journal of Medical Genetics. Part A|March 7, 2022
Exome and RNA-Seq analyses of an incomplete penetrance variant in USP9X in female-specific syndromic intellectual disabilityDong Li, Michael E March, Tiancheng Wang, et al.
Discovery Medicine|February 29, 2012
Mitochondrial tRNA-serine (AGY) m.C12264T mutation causes severe multisystem disease with cataractsSamantha A Schrier, Lee-Jun Wong, Emily Place, et al.
Pharmaceutical Research|January 12, 2002
Enhancement of bone growth by sustained delivery of recombinant human bone morphogenetic protein-2 in a polymeric matrixB H Woo, B F Fink, R Page, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Congenital heart disease in Cornelia de Lange syndrome: phenotype and genotype analysisKathryn C Chatfield, Samantha A Schrier, Jennifer Li, et al.
Pageof 8

Showing results (31-40 of 71) with videos related to

Sort By:
Pageof 8
The British Journal of Ophthalmology|May 1, 1996
Infectious keratitis with corneal perforation associated with corneal hydrops and contact lens wear in keratoconusE D Donnenfeld, A Schrier, H D Perry, et al.
American Journal of Medical Genetics. Part A|March 5, 2015
Mosaic trisomy 15 in a liveborn infantJacob McPadden, Benjamin M Helm, Brooke B Spangler, et al.
American Journal of Medical Genetics. Part A|July 7, 2022
Evidence for an association between Coffin-Siris syndrome and congenital diaphragmatic herniaYoel Gofin, Xiaonan Zhao, Amanda Gerard, et al.
American Journal of Medical Genetics. Part A|December 9, 2021
Further supporting SMARCC2-related neurodevelopmental disorder through exome analysis and reanalysis in two patientsDong Li, Helen Downes, Cuiping Hou, et al.
American Journal of Medical Genetics. Part A|September 5, 2015
Beyond Ohdo syndrome: A familial missense mutation broadens the MED12 spectrumKatherine G Langley, Jordan Brown, Richard J Gerber, et al.
Pharmaceutical Research|July 1, 1993
Degradation pathways for recombinant human macrophage colony-stimulating factor in aqueous solutionJ A Schrier, R A Kenley, R Williams, et al.
American Journal of Medical Genetics. Part A|March 7, 2022
Exome and RNA-Seq analyses of an incomplete penetrance variant in USP9X in female-specific syndromic intellectual disabilityDong Li, Michael E March, Tiancheng Wang, et al.
Discovery Medicine|February 29, 2012
Mitochondrial tRNA-serine (AGY) m.C12264T mutation causes severe multisystem disease with cataractsSamantha A Schrier, Lee-Jun Wong, Emily Place, et al.
Pharmaceutical Research|January 12, 2002
Enhancement of bone growth by sustained delivery of recombinant human bone morphogenetic protein-2 in a polymeric matrixB H Woo, B F Fink, R Page, et al.
American Journal of Medical Genetics. Part A|September 12, 2012
Congenital heart disease in Cornelia de Lange syndrome: phenotype and genotype analysisKathryn C Chatfield, Samantha A Schrier, Jennifer Li, et al.
Pageof 8