Preimplantation genetic diagnosis as a strategy to prevent having a child born with an heritable eye disease-Reference-Cited by-同舟云学术

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Preimplantation genetic diagnosis as a strategy to prevent having a child born with an heritable eye disease

Published:2018-05-21 Issue:4 Volume:39 Page:450-456
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Yahalom Claudia¹,Macarov Michal¹,Lazer-Derbeko Galit²,Altarescu Gheona²,Imbar Tal³,Hyman Jordana H.³,Eldar-Geva Talia⁴,Blumenfeld Anat¹

Affiliation:

1. Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel

2. Medical Genetics Institute, Shaare Zedek Medical Center, Jerusalem, Israel

3. Department of Obstetrics & Gynecology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel

4. Department of Obstetrics and Gynecology, Shaare Zedek Medical Center, Jerusalem, Israel

Publisher

Informa UK Limited

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2018.1474368

Reference45 articles.

1. An update on progress and the changing epidemiology of causes of childhood blindness worldwide

2. Changing trends over the last decade in the aetiology of childhood blindness: a study from a tertiary referral centre

3. Visual impairment in children born at full term from 1972 through 1989 in Finland

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1. Genetics of bilateral pediatric cataract in the Israeli and Palestinian populations;Graefe's Archive for Clinical and Experimental Ophthalmology;2024-06-14

2. Genetic counseling for pre-implantation genetic testing of monogenic disorders (PGT-M);Frontiers in Reproductive Health;2023-12-15

3. Preimplantation genetic testing for hereditary hearing loss in Chinese population;Journal of Assisted Reproduction and Genetics;2023-04-05

4. Comparing Gene Panels for Non-Retinal Indications: A Systematic Review;Genes;2023-03-17

5. Day 5 versus day 3 embryo biopsy for preimplantation genetic testing for monogenic/single gene defects;Cochrane Database of Systematic Reviews;2022-11-24

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