Early prenatal detection of short‐rib polydactyly syndrome in a monochorionic diamniotic twin pregnancy-Reference-Cited by-同舟云学术

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Early prenatal detection of short‐rib polydactyly syndrome in a monochorionic diamniotic twin pregnancy

Published:2018-11-15 Issue:5 Volume:59 Page:181-182
ISSN:0914-3505
Container-title:Congenital Anomalies
language:en
Short-container-title:Congenit Anom

Author:

Zhen Li¹,Huang Lv‐Yin¹,Li Dong‐Zhi¹^ORCID

Affiliation:

1. Guangzhou Women and Children's Medical Center, Guangzhou Medical College Guangdong China

Funder

Science and Technology Department of Guangdong Province

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cga.12317

Reference5 articles.

1. Ciliary disorder of the skeleton

2. Targeted gene panel sequencing prenatally detects two novel mutations of DYNC2H1 in a fetus with increased biparietal diameter and polyhydramnios

3. Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus

4. Prenatal diagnosis of skeletal dysplasias using a targeted skeletal gene panel

5. Polydactyly: phenotypes, genetics and classification

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