Imerslund-Gräsbeck syndrome: new mutation in amnionless. (Record no. 21811785)

MARC details
000 -LEADER
fixed length control field 01550 a2200433 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250516093559.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201210s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1442-200X
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1111/j.1442-200X.2011.03482.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 Densupsoontorn, Narumon
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20121001
245 00 - TITLE STATEMENT
Title Imerslund-Gräsbeck syndrome: new mutation in amnionless.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Pediatrics international : official journal of the Japan Pediatric Society
Date of publication, distribution, etc. Jun 2012
300 ## - PHYSICAL DESCRIPTION
Extent e19-21 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Case Reports; Journal Article
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Anemia, Megaloblastic
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Child, Preschool
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 Malabsorption Syndromes
General subdivision genetics
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 Membrane Proteins
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Mutation
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Proteins
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Proteinuria
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Vitamin B 12 Deficiency
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Sanpakit, Kleebsabai
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Vijarnsorn, Chodchanok
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pattaragarn, Aniruth
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kangwanpornsiri, Channagarn
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Jatutipsompol, Charnnarong
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Tirapongporn, Hathaichanok
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Jirapinyo, Pipop
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Shah, Nidhi P
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Sturm, Amy C
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Tanner, Stephan M
773 0# - HOST ITEM ENTRY
Title Pediatrics international : official journal of the Japan Pediatric Society
Related parts vol. 54
-- no. 3
-- p. e19-21
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1111/j.1442-200X.2011.03482.x">https://doi.org/10.1111/j.1442-200X.2011.03482.x</a>
Public note Available from publisher's website

No items available.