Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability | Journal of Medical Genetics

Subscribe
Log In More

Log in via Institution
Log in via OpenAthens
Log in via CCMG

Log in using your username and password
For personal accounts OR managers of institutional accounts

Username *

Password *

Forgot your log in details?Register a new account?
Forgot your user name or password?
Basket
Search More

Search for this keyword

Advanced search

Close More
Main menu

Latest content

Current issue

Archive

Authors

About

Topic collections
Subscribe
Log in More

Log in via Institution
Log in via OpenAthens
Log in via CCMG

Log in using your username and password
For personal accounts OR managers of institutional accounts

Username *

Password *

Forgot your log in details?Register a new account?
Forgot your user name or password?
BMJ Journals More

You are viewing from: Department GEZ-LTA Erasmushogeschool

Article metrics

PDF +
Supplementary
Material

Novel disease loci

Original research

Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability

Online download statistics by month:

Online download statistics by month: March 2024 to April 2025

	Abstract	Full	Pdf
Mar 2024	446	431	171
Apr 2024	330	323	110
May 2024	204	194	108
Jun 2024	416	408	117
Jul 2024	279	275	131
Aug 2024	168	153	85
Sep 2024	127	117	239
Oct 2024	121	110	379
Nov 2024	113	104	66
Dec 2024	131	124	95
Jan 2025	133	120	85
Feb 2025	157	155	66
Mar 2025	97	93	59
Apr 2025	123	109	63
Total	2845	2716	1774