Trio Clinical Exome Sequencing in a Patient With Multicentric Carpotarsal Osteolysis Syndrome: First Case Report in the Balkans. (Record no. 28306622)

MARC details
000 -LEADER
fixed length control field 01045 a2200289 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250517212348.0
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 1664-8021
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.3389/fgene.2018.00113
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 Stajkovska, Aleksandra
245 00 - TITLE STATEMENT
Title Trio Clinical Exome Sequencing in a Patient With Multicentric Carpotarsal Osteolysis Syndrome: First Case Report in the Balkans.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Frontiers in genetics
Date of publication, distribution, etc. 2018
300 ## - PHYSICAL DESCRIPTION
Extent 113 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Case Reports; Journal Article
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Mehandziska, Sanja
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Stavrevska, Margarita
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Jakovleva, Kristina
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Nikchevska, Natasha
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Mitrev, Zan
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kungulovski, Ivan
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Zafiroski, Gjorgje
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Tasic, Velibor
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kungulovski, Goran
773 0# - HOST ITEM ENTRY
Title Frontiers in genetics
Related parts vol. 9
-- p. 113
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.3389/fgene.2018.00113">https://doi.org/10.3389/fgene.2018.00113</a>
Public note Available from publisher's website

No items available.