Literature DB >> 34337849

Prenatal genetic screening and the evolving quest for "perfect babies": at what cost for genetic diversity?

Shina Caroline Lynn Kamerlin1.   

Abstract

Commercial screening services for inheritable diseases raise concerns about pressure on parents to terminate "imperfect babies".
© 2021 The Author.

Entities:  

Mesh:

Year:  2021        PMID: 34337849      PMCID: PMC8419682          DOI: 10.15252/embr.202153620

Source DB:  PubMed          Journal:  EMBO Rep        ISSN: 1469-221X            Impact factor:   9.071


  2 in total

Review 1.  GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing.

Authors:  Luigi Maione; Andrew A Dwyer; Bruno Francou; Anne Guiochon-Mantel; Nadine Binart; Jérôme Bouligand; Jacques Young
Journal:  Eur J Endocrinol       Date:  2018-01-12       Impact factor: 6.664

2.  Prenatal genetic screening and the evolving quest for "perfect babies": at what cost for genetic diversity?

Authors:  Shina Caroline Lynn Kamerlin
Journal:  EMBO Rep       Date:  2021-08-02       Impact factor: 9.071

  2 in total
  1 in total

1.  Prenatal genetic screening and the evolving quest for "perfect babies": at what cost for genetic diversity?

Authors:  Shina Caroline Lynn Kamerlin
Journal:  EMBO Rep       Date:  2021-08-02       Impact factor: 9.071

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.