Prenatal diagnosis of Greig Cephalopolysyndactyly Syndrome. When to suspect it.-Reference-Cited by-同舟云学术

Prenatal diagnosis of Greig Cephalopolysyndactyly Syndrome. When to suspect it.

Published:2020-06-04 Issue: Volume: Page:1-4
ISSN:1476-7058
Container-title:The Journal of Maternal-Fetal & Neonatal Medicine
language:en
Short-container-title:The Journal of Maternal-Fetal & Neonatal Medicine

Author:

Garcia-Rodriguez Raquel¹,Rodriguez-Rodriguez Raul¹,Garcia-Delgado Raquel¹,Romero-Requejo Azahar¹,Medina-Castellano Margarita¹,Garcia Cruz Loida²,Santana Rodriguez Alfredo²,Garcia-Hernandez Jose Angel¹

Affiliation:

1. Fetal Medicine Unit, Department of Obstetrics and Gynecology, Complejo Hospitalario Universitario Insular Materno Infantil, Las Palmas de Gran Canaria, Spain;

2. Clinical Genetics Unit, Complejo Hospitalario Universitario Insular Materno Infantil, Las Palmas de Gran Canaria, Spain

Publisher

Informa UK Limited

Subject

Obstetrics and Gynaecology,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/14767058.2020.1774541

Reference11 articles.

1. GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

2. Fetal biometry at 14-40 weeks' gestation

3. The Greig cephalopolysyndactyly syndrome

4. Greig Cephalopolysyndactyly Syndrome

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1. A Rare Prenatal Case: Greig Cephalopolysyndactyly Syndrome;Gazi Medical Journal;2024-04-01

2. Polyhydramnios associated with rare genetic syndromes: two case reports;Journal of Medical Case Reports;2024-02-19

3. Fetal Nasal Bone Hypoplasia in the Second Trimester as a Marker of Multiple Genetic Syndromes;Journal of Clinical Medicine;2022-03-10