Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Meagan Giles Choates"'
Autor:
Meagan Giles Choates, Maureen E. Mork, Sarah Noblin, Danielle Williams, S. Shakrukh Hashmi, Eduardo Vilar
Publikováno v:
Journal of Genetic Counseling. 29:728-736
Lynch syndrome (LS) is a hereditary cancer predisposition syndrome primarily defined by increased risk for colorectal and uterine cancers. Individuals with germline pathogenic variants in the mismatch repair (MMR) genes (MLH1, MSH2/EPCAM, MSH6, and P
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0242802cbed1bd7d297b55e630732fc4
https://doi.org/10.1002/jgc4.1198
https://doi.org/10.1002/jgc4.1198
Autor:
Claire N. Singletary, A. Theresa Wittman, Lauren Murphy, Blair K. Stevens, Meagan Giles Choates, Chelsea Wagner
Publikováno v:
Prenatal Diagnosis. 40:311-316
OBJECTIVE To describe uptake of carrier screening by male reproductive partners of prenatal and preconception patients. METHODS A retrospective database review of all prenatal and preconception patients seen for genetic counseling in Maternal Fetal M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::261bfc978ac28fb4bea85b69e69d6b6e
https://doi.org/10.1002/pd.5588
https://doi.org/10.1002/pd.5588
Autor:
Lauren Murphy, Chelsea Wagner, Meagan Giles Choates, Blair Stevens, Theresa Wittman, Aarti Ramdaney, Malorie Jones, Peyton B. Nunley
Publikováno v:
Prenatal diagnosisREFERENCES. 42(1)
OBJECTIVE Explore the utility of expanded carrier screening in evaluating heritable causes of congenital anomalies detected by prenatal ultrasound. METHOD A retrospective chart review was conducted to collect structural abnormality and genetic testin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::869870e63ee53963459224feb1c496ff
https://pubmed.ncbi.nlm.nih.gov/34792213
https://pubmed.ncbi.nlm.nih.gov/34792213
Autor:
Jennifer Czerwinski, Claire N. Singletary, Meagan Giles Choates, Chelsea Wagner, Nevena Krstić
Publikováno v:
Prenatal Diagnosis. 38:748-754
OBJECTIVE Characterize the uptake of chromosomal microarray analysis (CMA) among women undergoing invasive prenatal diagnosis at a large academic institution over a 4-year time period. METHODS Retrospective database review of women who underwent inva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dac9cf5d3e5d9b0128a46d855ed9632c
https://doi.org/10.1002/pd.5324
https://doi.org/10.1002/pd.5324