Yaron Y - Search Results

1

Novel causative mutations in patients with Nance-Horan syndrome and altered localization of the mutant NHS-A protein isoform.

Sharma S, Burdon KP, Dave A, Jamieson RV, Yaron Y, Billson F, Van Maldergem L, Lorenz B, Gécz J, Craig JE. Sharma S, et al. Among authors: yaron y. Mol Vis. 2008;14:1856-64. Epub 2008 Oct 20. Mol Vis. 2008. PMID: 18949062 Free PMC article.

2

Prenatal detection of congenital bilateral cataract leading to the diagnosis of Nance-Horan syndrome in the extended family.

Reches A, Yaron Y, Burdon K, Crystal-Shalit O, Kidron D, Malcov M, Tepper R. Reches A, et al. Among authors: yaron y. Prenat Diagn. 2007 Jul;27(7):662-4. doi: 10.1002/pd.1734. Prenat Diagn. 2007. PMID: 17451191

3

Novel mutations in the emerin gene in Israeli families.

Nevo Y, Ahituv S, Yaron Y, Kedmi M, Shomrat R, Legum C, Orr-Urtreger A. Nevo Y, et al. Among authors: yaron y. Hum Mutat. 2001 Jun;17(6):522. doi: 10.1002/humu.1139. Hum Mutat. 2001. PMID: 11385714

4

Preimplantation genetic diagnosis for fragile X syndrome: is there increased transmission of abnormal FMR1 alleles among female heterozygotes?

Reches A, Malcov M, Ben-Yosef D, Azem F, Amit A, Yaron Y. Reches A, et al. Among authors: yaron y. Prenat Diagn. 2009 Jan;29(1):57-61. doi: 10.1002/pd.2179. Prenat Diagn. 2009. PMID: 19097038

5

Resolving a genetic paradox throughout preimplantation genetic diagnosis for autosomal dominant severe congenital neutropenia.

Malcov M, Reches A, Ben-Yosef D, Cohen T, Amit A, Dgany O, Tamary H, Yaron Y. Malcov M, et al. Among authors: yaron y. Prenat Diagn. 2010 Mar;30(3):207-11. doi: 10.1002/pd.2437. Prenat Diagn. 2010. PMID: 20049848

6

Microscopic chromosome Xp distal deletions--a challenging issue in prenatal genetic counseling.

Sukenik-Halevy R, Reches A, Bar-Shira A, Simchoni S, Goldstein M, Orr-Ortreger A, Yaron Y, Ben-Shachar S. Sukenik-Halevy R, et al. Among authors: yaron y. Prenat Diagn. 2014 Jun;34(6):592-7. doi: 10.1002/pd.4354. Epub 2014 Mar 25. Prenat Diagn. 2014. PMID: 24609917

7

Preimplantation genetic diagnosis of Canavan disease.

Yaron Y, Schwartz T, Mey-Raz N, Amit A, Lessing JB, Malcov M. Yaron Y, et al. Fetal Diagn Ther. 2005 Sep-Oct;20(5):465-8. doi: 10.1159/000086834. Fetal Diagn Ther. 2005. PMID: 16113575

8

Preimplantation genetic diagnosis (PGD) for Duchenne muscular dystrophy (DMD) by triplex-nested PCR.

Malcov M, Ben-Yosef D, Schwartz T, Mey-Raz N, Azem F, Lessing JB, Amit A, Yaron Y. Malcov M, et al. Among authors: yaron y. Prenat Diagn. 2005 Dec;25(13):1200-5. doi: 10.1002/pd.1317. Prenat Diagn. 2005. PMID: 16353285

9

Association of aberrant right subclavian artery with abnormal karyotype and microarray results.

Svirsky R, Reches A, Brabbing-Goldstein D, Bar-Shira A, Yaron Y. Svirsky R, et al. Among authors: yaron y. Prenat Diagn. 2017 Aug;37(8):808-811. doi: 10.1002/pd.5092. Epub 2017 Jul 12. Prenat Diagn. 2017. PMID: 28618053

10

Familial Beckwith-Wiedemann syndrome: Prenatal manifestation and a possible expansion of the phenotype.

Brabbing-Goldstein D, Yaron Y, Reches A. Brabbing-Goldstein D, et al. Among authors: yaron y. Eur J Med Genet. 2021 Feb;64(2):104137. doi: 10.1016/j.ejmg.2021.104137. Epub 2021 Jan 6. Eur J Med Genet. 2021. PMID: 33421606

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

218 results

Search Page

Filters