Genetic Analysis of 1p36 Deletions for Six Aborted Fetuses
Source: Alternative Therapies in Health and Medicine
First-trimester application of expanded non-invasive prenatal testing in the genetic investigation of fetal 1p36 deletion syndrome associated with a familial unbalanced reciprocal translocation of 46,XX,der(1)t(1;2) (p36.2;q37.3)dmat
Source: Taiwanese Journal of Obstetrics and Gynecology
Estimating prevalence of rare genetic disease diagnoses using electronic health records in a children's hospital
Source: Human Genetics and Genomics Advances
Genetic Analysis of 1p36 Deletions for Six Aborted Fetuses
Source: Alternative therapies in health and medicine
Prenatal diagnosis of a fetus with 1p36 deletion syndrome and 3p26.3p25.2 duplication
Source: Chinese Journal of Medical Genetics
For Patient Families
To support patients and caregivers, Elsevier Health is making the latest research on these rare disorders available upon request at no cost.
Learn More
Note:
User acknowledges that these materials are provided for use at no charge as part of Elsevier’s efforts to support healthcare providers and patients. The information contained within the website is intended as a supplement to, and not a substitute for, the knowledge, expertise, skill and judgment of healthcare professionals involved in patient care. The content within this page may not be re-used, modified or re-distributed without prior written permission.
Cookies are used by this site. To decline or learn more, visit our cookie notice.
Copyright © 2024 Elsevier, its licensors, and contributors. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
