All individuals with variants in gene KCNQ1OT1

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

AscendingIndividual ID     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Disease     

Phenotype details     

Variants     

Panel size     

Owner     
00080096 23243085-Fet2 PubMed: Crescenzo 2013, for EUCID-SRS consortium family, 2 affected fetuses, fetus 1 affected similarly - - - - <00y00m - - - ?, SRS;RSS - 1 2 Zeynep Tümer
00290370 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00332518 patient PubMed: Eggermann 2021 2-generation family, 1 affected F no Germany - - - - - stature, short see paper; ..., 1 1 Johan den Dunnen
00443807 Pat511 PubMed: Imafidon 2021 prenatal indication abnormal ultrasound F - Netherlands - - - - - ? congenital omphalocele, dysmorphic features 1 1 Johan den Dunnen
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.