Skip to main content
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
Latest content
Current issue
Archive
Authors
About
Topic collections
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
You are here
Home
Archive
Volume 61, Issue 4
Heterozygous COL17A1 variants are a frequent cause of amelogenesis imperfecta
Email alerts
Article metrics
Article menu
Article
Text
Article
info
Citation
Tools
Share
Rapid Responses
Article
metrics
Alerts
PDF
PDF +
Supplementary
Material
Genotype-phenotype correlations
Original research
Heterozygous
COL17A1
variants are a frequent cause of amelogenesis imperfecta
Online download statistics by month:
Online download statistics by month: November 2023 to October 2024
Abstract
Full
Pdf
Nov 2023
283
284
96
Dec 2023
189
178
87
Jan 2024
167
137
53
Feb 2024
91
88
40
Mar 2024
342
326
98
Apr 2024
217
202
72
May 2024
111
99
52
Jun 2024
101
75
35
Jul 2024
111
101
33
Aug 2024
103
95
38
Sep 2024
91
71
31
Oct 2024
140
126
49
Total
1946
1782
684
Read the full text or download the PDF:
Subscribe
Log in
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?
PDF