Literature DB >> 35958070

Craniofrontonasal dysplasia.

Nisha Toteja1, Daisy Khera1, Rohit Sasidharan2.   

Abstract

Entities:  

Year:  2022        PMID： 35958070      PMCID： PMC9361484          DOI： 10.24911/SJP.106-1594635995

Source DB:  PubMed          Journal:  Sudan J Paediatr        ISSN： 0256-4408


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  4 in total

1.  Craniofrontonasal dysplasia associated with Chiari malformation.

Authors:  Amit Mahore; Abhidha Shah; Trimurti Nadkarni; Atul Goel
Journal:  J Neurosurg Pediatr       Date:  2010-04       Impact factor: 2.375

2.  Four novel mutations in EFNB1 in Indian patients with craniofrontonasal syndrome.

Authors:  Antonia Howaldt; Sheela Nampoothiri; Dhanya Yesodharan; Suhas Udayakumaran; Pramod Subash; Uwe Kornak
Journal:  J Hum Genet       Date:  2019-07-08       Impact factor: 3.172

Review 3.  Diverse clinical and genetic aspects of craniofrontonasal syndrome.

Authors:  Dimitrios I Zafeiriou; Efterpi L Pavlidou; Euthymia Vargìami
Journal:  Pediatr Neurol       Date:  2011-02       Impact factor: 3.372

4.  Craniofrontonasal Syndrome: Atrial Septal Defect With a Novel EFNB1 Gene Mutation.

Authors:  Manisha Goyal; Gaurav Pradhan; Ilse Wieland; Seema Kapoor
Journal:  Cleft Palate Craniofac J       Date:  2014-06-11
  4 in total

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