Literature DB >> 3346887

Craniofrontonasal dysplasia.

J Hurst, M Baraitser.   

Abstract

Entities:  

Mesh:

Year:  1988        PMID: 3346887      PMCID: PMC1015457          DOI: 10.1136/jmg.25.2.133

Source DB:  PubMed          Journal:  J Med Genet        ISSN: 0022-2593            Impact factor:   6.318


× No keyword cloud information.
  1 in total

1.  Craniofrontonasal dysplasia.

Authors:  I D Young
Journal:  J Med Genet       Date:  1987-04       Impact factor: 6.318

  1 in total
  3 in total

1.  Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1.

Authors:  M E P van den Elzen; S R F Twigg; J A C Goos; A J M Hoogeboom; A M W van den Ouweland; A O M Wilkie; I M J Mathijssen
Journal:  Eur J Hum Genet       Date:  2013-11-27       Impact factor: 4.246

2.  Craniofrontonasal dysplasia.

Authors:  L Kapusta; H G Brunner; B C Hamel
Journal:  Eur J Pediatr       Date:  1992-11       Impact factor: 3.183

3.  Case Report and Review of the Literature: Congenital Diaphragmatic Hernia and Craniosynostosis, a Coincidence or Common Cause?

Authors:  Linda Gaillard; Anne Goverde; Quincy C C van den Bosch; Fernanda S Jehee; Erwin Brosens; Danielle Veenma; Frank Magielsen; Annelies de Klein; Irene M J Mathijssen; Marieke F van Dooren
Journal:  Front Pediatr       Date:  2021-11-26       Impact factor: 3.418

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.