Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations-Reference-Cited by-同舟云学术

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Phenotypic Overlap of Roberts and Baller-Gerold Syndromes in Two Patients With Craniosynostosis, Limb Reductions, and ESCO2 Mutations

Published:2019-05-28 Issue: Volume:7 Page:
ISSN:2296-2360
Container-title:Frontiers in Pediatrics
language:
Short-container-title:Front. Pediatr.

Author:

Colombo Elisa Adele,Mutlu-Albayrak Hatice,Shafeghati Yousef,Balasar Mine,Piard Juliette,Gentilini Davide,Di Blasio Anna Maria,Gervasini Cristina,Van Maldergem Lionel,Larizza Lidia

Funder

Ministero della Salute

Publisher

Frontiers Media SA

Subject

Pediatrics, Perinatology, and Child Health

Reference43 articles.

1. Baller-Gerold Syndrome;Van Maldergem,1993

2. Roberts Syndrome;Gordillo,1993

3. Osteosarcoma in a 16-year-old boy with Baller-Gerold syndrome;Preis;Clin Dysmorphol.,1995

4. A patient with Baller-Gerold syndrome and midline NK/T lymphoma;Debeljak;Am J Med Genet A.,2009

5. Fanconi anemia in a child previously diagnosed as Baller-Gerold syndrome;Farrell;Am J Med Genet.,1994

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. CLINICAL AND MOLECULAR RESULTS OF SIX CASES WITH ROBERTS SYNDROME: REVIEW OF CASES FROM TURKIYE;Journal of Istanbul Faculty of Medicine / İstanbul Tıp Fakültesi Dergisi;2022-10-17

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