Apert's syndrome: Study by whole exome sequencing. (Record no. 28878092)

MARC details
000 -LEADER
fixed length control field 00844 a2200253 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250518001139.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field ####s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 2352-3042
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1016/j.gendis.2017.07.008
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 Munshi, Anjana
245 00 - TITLE STATEMENT
Title Apert's syndrome: Study by whole exome sequencing.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Genes & diseases
Date of publication, distribution, etc. Jun 2018
300 ## - PHYSICAL DESCRIPTION
Extent 119-122 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Khetarpal, Preeti
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Das, Satrupa
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Rao, Venkateshwar
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Valecha, Monica
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Bansal, Manita
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kumar, Roshan
773 0# - HOST ITEM ENTRY
Title Genes & diseases
Related parts vol. 5
-- no. 2
-- p. 119-122
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1016/j.gendis.2017.07.008">https://doi.org/10.1016/j.gendis.2017.07.008</a>
Public note Available from publisher's website

No items available.