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Genomic Alterations Are Enhanced in Placentas from Pregnancies with Fetal Growth Restriction and Preeclampsia: Preliminary Results.
Mol Syndromol. 2016 Feb;6(6):276-80. doi: 10.1159/000444064. Epub 2016 Jan 27.
Mol Syndromol. 2016.
PMID: 27022328
Free PMC article.
Prenatal course of metaphyseal anadysplasia associated with homozygous mutation in MMP9 identified by exome sequencing.
Sharony R, Borochowitz Z, Cohen L, Shtorch-Asor A, Rosenfeld R, Modai S, Reinstein E.
Sharony R, et al. Among authors: shtorch asor a.
Clin Genet. 2017 Dec;92(6):645-648. doi: 10.1111/cge.13020. Epub 2017 Aug 3.
Clin Genet. 2017.
PMID: 28342220
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Large scale population screening for Duchenne muscular dystrophy-Predictable and unpredictable challenges.
Cohen G, Shtorch-Asor A, Ben-Shachar S, Goldfarb-Yaacobi R, Kaiser M, Rosenfeld R, Vinovezky M, Irge D, Furman Y, Reiss D, Litz-Philipsborn S, Sukenik-Halevy R.
Cohen G, et al. Among authors: shtorch asor a.
Prenat Diagn. 2022 Aug;42(9):1162-1172. doi: 10.1002/pd.6201. Epub 2022 Jul 5.
Prenat Diagn. 2022.
PMID: 35751502
Free PMC article.
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A founder mutation in TCTN2 causes Meckel-Gruber syndrome type 8 among Jews of Ethiopian and Yemenite origin.
Litz Philipsborn S, Hartmajer S, Shtorch Asor A, Vinovezky M, Regev M, Singer A, Reinstein E.
Litz Philipsborn S, et al. Among authors: shtorch asor a.
Am J Med Genet A. 2021 May;185(5):1610-1613. doi: 10.1002/ajmg.a.62119. Epub 2021 Feb 15.
Am J Med Genet A. 2021.
PMID: 33590725
No abstract available.
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Hyper IgE Syndrome in an Isolated Population in Israel.
Lachover-Roth I, Lagovsky I, Shtorch-Asor A, Confino-Cohen R, Reinstein E, Garty BZ.
Lachover-Roth I, et al. Among authors: shtorch asor a.
Front Immunol. 2022 Feb 4;13:829239. doi: 10.3389/fimmu.2022.829239. eCollection 2022.
Front Immunol. 2022.
PMID: 35185921
Free PMC article.
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