Literature DB >> 32681669

De novo HRAS gene mutation associated with Costello syndrome identified by non-invasive cell-free fetal DNA screening.

Chidinma Nwakalor1, Sara Said-Delgado2, Shifra Krinshpun3, Milen Velinov4,5.   

Abstract

Entities:  

Year:  2020        PMID: 32681669     DOI: 10.1002/pd.5798

Source DB:  PubMed          Journal:  Prenat Diagn        ISSN: 0197-3851            Impact factor:   3.050


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  1 in total

1.  Clinical experience with non-invasive prenatal screening for single-gene disorders.

Authors:  P Mohan; J Lemoine; C Trotter; I Rakova; P Billings; S Peacock; C-Y Kao; Y Wang; F Xia; C M Eng; P Benn
Journal:  Ultrasound Obstet Gynecol       Date:  2022-01       Impact factor: 8.678

  1 in total

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