RUNX2 mutations in cleidocranial dysplasia patients. (Record no. 19142566)

MARC details
000 -LEADER
fixed length control field 01245 a2200385 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250515184954.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201006s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1601-0825
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1111/j.1601-0825.2009.01623.x
Source of number or code doi
040 ## - CATALOGING SOURCE
Original cataloging agency NLM
Language of cataloging eng
Transcribing agency NLM
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Ryoo, H-M
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20100618
245 00 - TITLE STATEMENT
Title RUNX2 mutations in cleidocranial dysplasia patients.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Oral diseases
Date of publication, distribution, etc. Jan 2010
300 ## - PHYSICAL DESCRIPTION
Extent 55-60 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article; Research Support, Non-U.S. Gov't
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Child
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Cleidocranial Dysplasia
General subdivision complications
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Codon, Nonsense
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Core Binding Factor Alpha 1 Subunit
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element DNA Mutational Analysis
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Female
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Humans
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Male
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Mutation, Missense
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Pedigree
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Polymorphism, Single Nucleotide
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Tooth, Supernumerary
General subdivision etiology
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kang, H-Y
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Lee, S-K
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Lee, K-E
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kim, J-W
773 0# - HOST ITEM ENTRY
Title Oral diseases
Related parts vol. 16
-- no. 1
-- p. 55-60
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1111/j.1601-0825.2009.01623.x">https://doi.org/10.1111/j.1601-0825.2009.01623.x</a>
Public note Available from publisher's website

No items available.