Complex 4q35 and 10q26 Rearrangements-Reference-Cited by-同舟云学术

Complex 4q35 and 10q26 Rearrangements

Published:2023-06 Issue:3 Volume:9 Page:
ISSN:2376-7839
Container-title:Neurology Genetics
language:en
Short-container-title:Neurol Genet

Author:

Delourme Megane¹,Charlene Chaix¹,Gerard Laurene¹,Ganne Benjamin¹,Perrin Pierre¹,Vovan Catherine¹,Bertaux Karine¹,Nguyen Karine¹,Bernard Rafaëlle¹,Magdinier Frederique¹^ORCID

Affiliation:

1. From the Aix Marseille University (M.D., B.G., P.P., K.N., R.B., F.M.), INSERM; Département de Génétique Médicale (C.C., L.G., C.V., K.B., K.N., R.B.), and Centre de Ressources Biologiques (K.B.), AP-HM, Hôpital d'enfants de la Timone, Marseille, France.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Genetics (clinical),Neurology (clinical)

Link

https://www.neurology.org/doi/pdfdirect/10.1212/NXG.0000000000200076

Reference44 articles.

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3. Facioscapulohumeral muscular dystrophy

4. Pulsed-Field Gel Electrophoresis of the D4F104S1 Locus Reveals the Size and the Parental Origin of the Facioscapulohumeral Muscular Dystrophy (FSHD)-Associated Deletions

5. Regional mapping of facioscapulohumeral muscular dystrophy gene on 4q35: combined analysis of an international consortium;Sarfarazi M;Am J Hum Genet.,1992

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