Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features-Reference-Cited by-同舟云学术

Int22h1/Int22h2 ‐mediated Xq28 duplication syndrome: de novo duplications, prenatal diagnoses, and additional phenotypic features

Published:2020-03-12 Issue:7 Volume:41 Page:1238-1249
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Human Mutation

Author:

Ballout Rami A.¹²^ORCID,Dickerson Cheryl³,Wick Myra J.⁴,Al‐Sweel Najla⁵⁶,Openshaw Amanda S.⁶,Srivastava Siddharth⁷,Swanson Lindsay C.⁷,Bramswig Nuria C.⁸,Kuechler Alma⁸,Hong Bo⁵⁶,Fleming Leah R.⁹,Curry Kathryn⁹,Robertson Stephen P.¹⁰,Andersen Erica F.⁵⁶,El‐Hattab Ayman W.¹¹^ORCID

Affiliation:

1. Lipoprotein Metabolism Section, Translational Vascular Medicine Branch, National Heart, Lung, and Blood InstituteNational Institutes of Health Bethesda Maryland

2. Faculty of MedicineAmerican University of Beirut Beirut Lebanon

3. WakeMed Physician PracticesMaternal–Fetal Medicine Raleigh North Carolina

4. Departments of Obstetrics and Gynecology and Clinical GenomicsMayo Clinic Rochester Minnesota

5. Department of PathologyUniversity of Utah Salt Lake City Utah

6. ARUP LaboratoriesCytogenetics and Genomic Microarray Salt Lake City Utah

7. Department of NeurologyBoston Children's Hospital Boston Massachusetts

8. Institut für Humangenetik, Universitätsklinikum EssenUniversität Duisburg‐Essen Essen Germany

9. St. Luke's Children's Genetics and Metabolic Clinic Boise Idaho

10. Department of Women's and Children's Health, Dunedin School of MedicineUniversity of Otago Dunedin New Zealand

11. Department of Clinical Sciences, College of MedicineUniversity of Sharjah Sharjah UAE

Funder

National Heart, Lung, and Blood Institute