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Dana Brabbing-Goldstein

Tel Aviv Sourasky Medical Center

5

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19

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Ethnicity has a multiplex impact upon the risk of a full mutation expansion among female heterozygotes for FMR1 premutation.

2021 Genetics in Medicine
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Familial Beckwith-Wiedemann syndrome: Prenatal manifestation and a possible expansion of the phenotype.

2021 European Journal of Medical Genetics
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The genetic and clinical outcome of isolated fetal muscular ventricular septal defect (VSD)

2018 Journal of Maternal-fetal & Neonatal Medicine
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Association of aberrant right subclavian artery with abnormal karyotype and microarray results

2017 Prenatal Diagnosis
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160: Chromosomal microarray for patient choice disadvantage may outweigh benefit

2017 American Journal of Obstetrics and Gynecology
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