A Case of the 7p22.2 Microduplication: Refinement of the Critical Chromosome Region for 7p22 Duplication Syndrome. (Record no. 26408889)

MARC details
000 -LEADER
fixed length control field 00798 a2200205 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250517114259.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201609s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 2146-4596
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1055/s-0035-1554980
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 Cox, Devin M
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20160912
245 00 - TITLE STATEMENT
Title A Case of the 7p22.2 Microduplication: Refinement of the Critical Chromosome Region for 7p22 Duplication Syndrome.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Journal of pediatric genetics
Date of publication, distribution, etc. Mar 2015
300 ## - PHYSICAL DESCRIPTION
Extent 34-7 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Case Reports; Journal Article
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Butler, Merlin G
773 0# - HOST ITEM ENTRY
Title Journal of pediatric genetics
Related parts vol. 4
-- no. 1
-- p. 34-7
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1055/s-0035-1554980">https://doi.org/10.1055/s-0035-1554980</a>
Public note Available from publisher's website

No items available.