It takes two: uptake of carrier screening among male reproductive partners-Reference-Cited by-同舟云学术

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It takes two: uptake of carrier screening among male reproductive partners

Published:2019-12-02 Issue:3 Volume:40 Page:311-316
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenatal Diagnosis

Author:

Giles Choates Meagan¹²^ORCID,Stevens Blair K.¹²,Wagner Chelsea¹²,Murphy Lauren¹²,Singletary Claire N.¹²³^ORCID,Wittman A. Theresa¹²

Affiliation:

1. Department of Obstetrics, Gynecology, and Reproductive SciencesMcGovern Medical School at UTHealth Houston TX USA

2. UT MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences Houston TX USA

3. Department of PediatricsMcGovern Medical School at UTHealth Houston TX USA

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.5588

Reference21 articles.

1. Committee Opinion No. 691: Carrier Screening for Genetic Conditions

2. An empirical estimate of carrier frequencies for 400+ causal Mendelian variants: results from an ethnically diverse clinical sample of 23,453 individuals

3. Perceived relevance of genetic carrier screening: observations of the role of health-related life experiences and stage of life in decision making

4. “I'm Healthy, It's Not Going To Be Me”: Exploring experiences of carriers identified through a population reproductive genetic carrier screening panel in Australia

5. Reasons for Declining Preconception Expanded Carrier Screening Using Genome Sequencing

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1. Cell-Free DNA Analysis for the Determination of Fetal Red Blood Cell Antigen Genotype in Individuals With Alloimmunized Pregnancies;Obstetrics & Gynecology;2024-07-25

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3. Response to the correspondence on “Performance of single‐gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting”;Prenatal Diagnosis;2024-01-09

4. A comprehensive view of pregnancy in patients with sickle cell disease in high-income countries: the need for robust data and further decline in morbidity and mortality;The Lancet Haematology;2024-01

5. Current controversy in prenatal diagnosis: The use of cfDNA to screen for monogenic conditions in low risk populations is ready for clinical use;Prenatal Diagnosis;2023-11-22

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