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Case Reports in Genetics
|
October 18, 2012
Clinical findings associated with a de novo partial trisomy 10p11.22p15.3 and monosomy 7p22.3 detected by chromosomal microarray analysis
Omid Kohannim, Jane Peredo, Katrina M Dipple, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
March 28, 2012
Cleft Lip and Palate in a Patient with 5q35.2-q35.3 Microdeletion: The Importance of Chromosomal Microarray Testing in the Craniofacial Clinic
Jane Peredo, Fabiola Quintero-Rivera, James P Bradley, et al.
Federal Practitioner : for the Health Care Professionals of the VA, Dod, and PHS
|
September 10, 2020
Integrating Germline Genetics Into Precision Oncology Practice in the Veterans Health Administration: Challenges and Opportunities
Maren T Scheuner, Kenute Myrie, Jane Peredo, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2014
Duodenal atresia in 17q12 microdeletion including HNF1B: a new associated malformation in this syndrome
Fabiola Quintero-Rivera, Jennifer S Woo, Eric M Bomberg, et al.
Molecular Genetics and Metabolism
|
September 7, 2010
An exon 1 deletion in OTC identified using chromosomal microarray analysis in a mother and her two affected deceased newborns: implications for the prenatal diagnosis of ornithine transcarbamylase deficiency
Fabiola Quintero-Rivera, Joshua L Deignan, Jane Peredo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 14, 2014
Reporting genomic secondary findings: ACMG members weigh in
Maren T Scheuner, Jane Peredo, Judith Benkendorf, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 25, 2018
A logic model for precision medicine implementation informed by stakeholder views and implementation science
Catherine Chanfreau-Coffinier, Jane Peredo, Marcia M Russell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 1, 2018
Stakeholders' views on the value of outcomes from clinical genetic and genomic interventions
Maren T Scheuner, Marcia M Russell, Catherine Chanfreau-Coffinier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 1, 2016
Electronic health record interventions at the point of care improve documentation of care processes and decrease orders for genetic tests commonly ordered by nongeneticists
Maren T Scheuner, Jane Peredo, Kelly Tangney, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 15, 2013
A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians
Maren T Scheuner, Alison B Hamilton, Jane Peredo, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 10) with videos related to
Sort By:
Page
of 1
Case Reports in Genetics
|
October 18, 2012
Clinical findings associated with a de novo partial trisomy 10p11.22p15.3 and monosomy 7p22.3 detected by chromosomal microarray analysis
Omid Kohannim, Jane Peredo, Katrina M Dipple, et al.
The Cleft Palate-Craniofacial Journal : Official Publication of the American Cleft Palate-Craniofacial Association
|
March 28, 2012
Cleft Lip and Palate in a Patient with 5q35.2-q35.3 Microdeletion: The Importance of Chromosomal Microarray Testing in the Craniofacial Clinic
Jane Peredo, Fabiola Quintero-Rivera, James P Bradley, et al.
Federal Practitioner : for the Health Care Professionals of the VA, Dod, and PHS
|
September 10, 2020
Integrating Germline Genetics Into Precision Oncology Practice in the Veterans Health Administration: Challenges and Opportunities
Maren T Scheuner, Kenute Myrie, Jane Peredo, et al.
American Journal of Medical Genetics. Part A
|
September 27, 2014
Duodenal atresia in 17q12 microdeletion including HNF1B: a new associated malformation in this syndrome
Fabiola Quintero-Rivera, Jennifer S Woo, Eric M Bomberg, et al.
Molecular Genetics and Metabolism
|
September 7, 2010
An exon 1 deletion in OTC identified using chromosomal microarray analysis in a mother and her two affected deceased newborns: implications for the prenatal diagnosis of ornithine transcarbamylase deficiency
Fabiola Quintero-Rivera, Joshua L Deignan, Jane Peredo, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 14, 2014
Reporting genomic secondary findings: ACMG members weigh in
Maren T Scheuner, Jane Peredo, Judith Benkendorf, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 25, 2018
A logic model for precision medicine implementation informed by stakeholder views and implementation science
Catherine Chanfreau-Coffinier, Jane Peredo, Marcia M Russell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
November 1, 2018
Stakeholders' views on the value of outcomes from clinical genetic and genomic interventions
Maren T Scheuner, Marcia M Russell, Catherine Chanfreau-Coffinier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 1, 2016
Electronic health record interventions at the point of care improve documentation of care processes and decrease orders for genetic tests commonly ordered by nongeneticists
Maren T Scheuner, Jane Peredo, Kelly Tangney, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 15, 2013
A cancer genetics toolkit improves access to genetic services through documentation and use of the family history by primary-care clinicians
Maren T Scheuner, Alison B Hamilton, Jane Peredo, et al.
Page
of 1