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Jan M Friedman

Showing results (111-120 of 165) with videos related to

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Journal of Medical Genetics|June 5, 2007
Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three childrenFarah Zahir, Helen V Firth, Agnes Baross, et al.
Pharmacoepidemiology and Drug Safety|July 30, 2013
Medications in the first trimester of pregnancy: most common exposures and critical gaps in understanding fetal riskPhoebe G Thorpe, Suzanne M Gilboa, Sonia Hernandez-Diaz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
The cost and diagnostic yield of exome sequencing for children with suspected genetic disorders: a benchmarking studyNick Dragojlovic, Alison M Elliott, Shelin Adam, et al.
Pharmacoepidemiology and Drug Safety|January 30, 2013
Safe lists for medications in pregnancy: inadequate evidence base and inconsistent guidance from Web-based information, 2011Stacey L Peters, Jennifer N Lind, Jasmine R Humphrey, et al.
American Journal of Medical Genetics. Part A|October 18, 2016
Intragenic CNVs for epigenetic regulatory genes in intellectual disability: Survey identifies pathogenic and benign single exon changesFarah R Zahir, Tracy Tucker, Sonia Mayo, et al.
American Journal of Medical Genetics. Part A|December 12, 2025
Identification of Compound Heterozygous CYP11A1 Variants via Reanalysis of Clinical Sequencing DataAna Acosta Bedón, Vahid Akbari, Ralph Rothstein, et al.
Journal of Genetic Counseling|July 24, 2018
Assessing an Interactive Online Tool to Support Parents' Genomic Testing DecisionsShelin Adam, Patricia H Birch, Rachel R Coe, et al.
JAMA Network Open|July 10, 2024
Health Care Costs After Genome-Wide Sequencing for Children With Rare Diseases in England and CanadaDeirdre Weymann, John Buckell, Patrick Fahr, et al.
JAMA Pediatrics|March 20, 2018
Key Implications of Data Sharing in Pediatric GenomicsVasiliki Rahimzadeh, Christoph Schickhardt, Bartha M Knoppers, et al.
Orphanet Journal of Rare Diseases|January 29, 2014
A novel recurrent mutation in ATP1A3 causes CAPOS syndromeMichelle K Demos, Clara Dm van Karnebeek, Colin Jd Ross, et al.
Pageof 17

Showing results (111-120 of 165) with videos related to

Sort By:
Pageof 17
Journal of Medical Genetics|June 5, 2007
Novel deletions of 14q11.2 associated with developmental delay, cognitive impairment and similar minor anomalies in three childrenFarah Zahir, Helen V Firth, Agnes Baross, et al.
Pharmacoepidemiology and Drug Safety|July 30, 2013
Medications in the first trimester of pregnancy: most common exposures and critical gaps in understanding fetal riskPhoebe G Thorpe, Suzanne M Gilboa, Sonia Hernandez-Diaz, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 5, 2018
The cost and diagnostic yield of exome sequencing for children with suspected genetic disorders: a benchmarking studyNick Dragojlovic, Alison M Elliott, Shelin Adam, et al.
Pharmacoepidemiology and Drug Safety|January 30, 2013
Safe lists for medications in pregnancy: inadequate evidence base and inconsistent guidance from Web-based information, 2011Stacey L Peters, Jennifer N Lind, Jasmine R Humphrey, et al.
American Journal of Medical Genetics. Part A|October 18, 2016
Intragenic CNVs for epigenetic regulatory genes in intellectual disability: Survey identifies pathogenic and benign single exon changesFarah R Zahir, Tracy Tucker, Sonia Mayo, et al.
American Journal of Medical Genetics. Part A|December 12, 2025
Identification of Compound Heterozygous CYP11A1 Variants via Reanalysis of Clinical Sequencing DataAna Acosta Bedón, Vahid Akbari, Ralph Rothstein, et al.
Journal of Genetic Counseling|July 24, 2018
Assessing an Interactive Online Tool to Support Parents' Genomic Testing DecisionsShelin Adam, Patricia H Birch, Rachel R Coe, et al.
JAMA Network Open|July 10, 2024
Health Care Costs After Genome-Wide Sequencing for Children With Rare Diseases in England and CanadaDeirdre Weymann, John Buckell, Patrick Fahr, et al.
JAMA Pediatrics|March 20, 2018
Key Implications of Data Sharing in Pediatric GenomicsVasiliki Rahimzadeh, Christoph Schickhardt, Bartha M Knoppers, et al.
Orphanet Journal of Rare Diseases|January 29, 2014
A novel recurrent mutation in ATP1A3 causes CAPOS syndromeMichelle K Demos, Clara Dm van Karnebeek, Colin Jd Ross, et al.
Pageof 17