Concepedia

Rebecca Sahraoui

RS

Statistics

Publications

3

Citations

292

H-Index

3

Active since

2014

Affiliations

Alfred I. duPont Hospital for Children(Current)

University of Delaware

University of Washington

Rebecca Sahraoui is an author at Alfred I. duPont Hospital for Children specializing in genetic disorders, life sciences, and molecular genetics.

Publications per year

2014–2018

3

Publications

3

Diamond–Blackfan anemia with mandibulofacial dystostosis is heterogeneous, including the novel DBA genes <i>TSR2</i> and <i>RPS28</i>

Karen W. Gripp, Cynthia J. Curry, Ann Haskins Olney et al. · American Journal of Medical Genetics Part A · 2014 · 148 citations · Full text

, , +17

GGC Repeat Expansion and Exon 1 Methylation of XYLT1 Is a Common Pathogenic Variant in Baratela-Scott Syndrome

Amy Lacroix, Deborah L. Stabley, Rebecca Sahraoui et al. · The American Journal of Human Genetics · 2018 · 115 citations · Full text

, , +12

Paternal uniparental disomy with segmental loss of heterozygosity of chromosome 11 are hallmark characteristics of syndromic and sporadic embryonal rhabdomyosarcoma

Katherine Robbins, Deborah L. Stabley, Jennifer Holbrook et al. · American Journal of Medical Genetics Part A · 2016 · 29 citations

, , +17

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