Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases. (Record no. 1839140)

MARC details
000 -LEADER
fixed length control field 01312 a2200409 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250511205805.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 199111s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0007-1048
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1111/j.1365-2141.1991.tb04487.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 Iolascon, A
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 19911107
245 00 - TITLE STATEMENT
Title Ankyrin deficiency in dominant hereditary spherocytosis: report of three cases.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. British journal of haematology
Date of publication, distribution, etc. Aug 1991
300 ## - PHYSICAL DESCRIPTION
Extent 551-4 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Adolescent
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Adult
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Ankyrins
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Blood Proteins
General subdivision deficiency
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Electrophoresis, Polyacrylamide Gel
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 Membrane Proteins
General subdivision deficiency
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 Spectrin
General subdivision deficiency
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Spherocytosis, Hereditary
General subdivision blood
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Miraglia del Giudice, E
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Camaschella, C
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Pinto, L
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Nobili, B
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Perrotta, S
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Cutillo, S
773 0# - HOST ITEM ENTRY
Title British journal of haematology
Related parts vol. 78
-- no. 4
-- p. 551-4
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1111/j.1365-2141.1991.tb04487.x">https://doi.org/10.1111/j.1365-2141.1991.tb04487.x</a>
Public note Available from publisher's website

No items available.