Occurrence of c.976 G>T (p.Val326Leu) and c.452 G>A (p.Trp151Ter) variants in DHCR7 gene in population of polish women with recurrent miscarriage-Reference-Cited by-同舟云学术

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Occurrence of c.976 G>T (p.Val326Leu) and c.452 G>A (p.Trp151Ter) variants in DHCR7 gene in population of polish women with recurrent miscarriage

Published:2020-09 Issue: Volume:252 Page:252-255
ISSN:0301-2115
Container-title:European Journal of Obstetrics & Gynecology and Reproductive Biology
language:en
Short-container-title:European Journal of Obstetrics & Gynecology and Reproductive Biology

Author:

Chrzanowska - Steglińska Marta^ORCID,Moczulska Hanna,Skoczylas Beata,Pietrusiński Michał,Antosik Karolina,Jakiel Paulina,Kacprzak Marta,Borowiec Maciej,Sieroszewski Piotr

Funder

Medical University of Lodz

Publisher

Elsevier BV

Subject

Obstetrics and Gynaecology,Reproductive Medicine

Reference20 articles.

1. Genetic causes of recurrent miscarriages;Kacprzak;Ginekol Pol,2016

2. Prenatal death in Smith-Lemli-Opitz/RSH syndrome;Putnam;Am J Med Genet A,2005

3. SLOS carrier frequency in Poland as determined by screening for Trp151X and Val326Leu DHCR7 mutations;Ciara;Eur J Med Genet,2006

4. Phenotypic spectrum of fetal Smith-Lemli-Opitz syndrome;Quélin;Eur J Med Genet,2012

5. Prenatal diagnostic of Smith-Lemli-Opitz syndrome;Moczulska;Prenat Cardio,2012

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