Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndrome-Reference-Cited by-同舟云学术

Sprengel anomaly in deletion 22q11.2 (DiGeorge/Velo-Cardio-Facial) syndrome

Published:2015-12-21 Issue:3 Volume:170 Page:661-664
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Radio Francesca Clementina¹,Digilio Maria Cristina¹,Capolino Rossella¹,Dentici Maria Lisa¹,Unolt Marta²,Alesi Viola¹,Novelli Antonio¹,Marino Bruno²,Dallapiccola Bruno¹

Affiliation:

1. Medical Genetic Unit and Laboratory of Medical Genetics; Bambino Gesù Pediatric Hospital, IRCCS; Rome Italy

2. Department of Pediatrics; Sapienza University; Rome Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.37503/fullpdf

Reference29 articles.

1. Generalized skeletal dysplasia in mother and daughter with 22q11 deletion syndrome;Adachi;Am J Med Genet Part A,2003

2. Orthopaedic manifestations of Goldenhar syndrome;Avon;J Pediatr Orthop,1988

3. Subclavian artery supply disruption sequence: Hypothesis of a vascular etiology for Poland, Klippel-Feil, and Möbius anomalies;Bavinck;Am J Med Genet,1986

4. Congenital elevation of the scapula;Cavendish;J Bone Joint Surg Br,1972

5. Upper limb malformations in DiGeorge syndrome;Cormier-Daire;Am J Med Genet,1995

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1. Sprengel Deformity;Congenital and Acquired Deformities of the Pediatric Shoulder Girdle;2022

2. Skeletal anomalies associated with 22q11.2 deletion syndrome;The Chromosome 22q11.2 Deletion Syndrome;2022

3. Functional improvement in patients with Sprengel’s deformity following Modified Green’s procedure and simplified clavicle osteotomy—a study of forty cases;International Orthopaedics;2020-10-23