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Journal of Genetic Counseling
|
April 27, 2023
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities
Chelsea Stevens, Hannah Llorin, Camila Gabriel, et al.
Orphanet Journal of Rare Diseases
|
May 11, 2021
Rare disease patient matchmaking: development and outcomes of an internet case-finding strategy in the Undiagnosed Diseases Network
Kimberly LeBlanc, Emily Glanton, Anna Nagy, et al.
Prenatal Diagnosis
|
April 10, 2023
Postnatal genetic testing on cord blood for prenatally identified high-probability cases
Sophie Adams, Hannah Llorin, Lori J Dobson, et al.
Prenatal Diagnosis
|
September 30, 2022
Chromosomal microarray analysis in pregnancy loss: Is it time for a consensus approach?
Samantha L P Schilit, Courtney Studwell, Pamela Flatley, et al.
American Journal of Medical Genetics. Part A
|
March 18, 2026
Experiences With Detection of Higher-Copy Sex Chromosome Aneuploidy by cfDNA Screening: The Critical Role of Diagnostic Testing
Lauren A Choate, Courtney Studwell, David T Miller, et al.
Experimental and Molecular Pathology
|
March 20, 2018
Rural distribution of human papilloma virus in low- and middle-income countries
Aaron Atkinson, Courtney Studwell, Suyapa Bejarano, et al.
Clinical Chemistry
|
January 3, 2025
Routine Prenatal cfDNA Screening for Autosomal Dominant Single-Gene Conditions
Sophie Adams, Olivia Maher Trocki, Christina Miller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 30, 2021
Utility of noninvasive genome-wide screening: a prospective cohort of obstetric patients undergoing diagnostic testing
Stephanie Guseh, Louise Wilkins-Haug, Anjali Kaimal, et al.
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of 1
Search research articles
Search
Showing results (1-10 of 8) with videos related to
Sort By:
Page
of 1
Journal of Genetic Counseling
|
April 27, 2023
Genetic counseling for fetal sex prediction by NIPT: Challenges and opportunities
Chelsea Stevens, Hannah Llorin, Camila Gabriel, et al.
Orphanet Journal of Rare Diseases
|
May 11, 2021
Rare disease patient matchmaking: development and outcomes of an internet case-finding strategy in the Undiagnosed Diseases Network
Kimberly LeBlanc, Emily Glanton, Anna Nagy, et al.
Prenatal Diagnosis
|
April 10, 2023
Postnatal genetic testing on cord blood for prenatally identified high-probability cases
Sophie Adams, Hannah Llorin, Lori J Dobson, et al.
Prenatal Diagnosis
|
September 30, 2022
Chromosomal microarray analysis in pregnancy loss: Is it time for a consensus approach?
Samantha L P Schilit, Courtney Studwell, Pamela Flatley, et al.
American Journal of Medical Genetics. Part A
|
March 18, 2026
Experiences With Detection of Higher-Copy Sex Chromosome Aneuploidy by cfDNA Screening: The Critical Role of Diagnostic Testing
Lauren A Choate, Courtney Studwell, David T Miller, et al.
Experimental and Molecular Pathology
|
March 20, 2018
Rural distribution of human papilloma virus in low- and middle-income countries
Aaron Atkinson, Courtney Studwell, Suyapa Bejarano, et al.
Clinical Chemistry
|
January 3, 2025
Routine Prenatal cfDNA Screening for Autosomal Dominant Single-Gene Conditions
Sophie Adams, Olivia Maher Trocki, Christina Miller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 30, 2021
Utility of noninvasive genome-wide screening: a prospective cohort of obstetric patients undergoing diagnostic testing
Stephanie Guseh, Louise Wilkins-Haug, Anjali Kaimal, et al.
Page
of 1