Severe poikilocytosis associated with a de novo alpha 28 Arg-->Cys mutation in spectrin. (Record no. 8434593)

MARC details
000 -LEADER
fixed length control field 01370 a2200421 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250513080336.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 199303s 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.1365-2141.1993.tb04646.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 Lorenzo, F
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 19930324
245 00 - TITLE STATEMENT
Title Severe poikilocytosis associated with a de novo alpha 28 Arg-->Cys mutation in spectrin.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. British journal of haematology
Date of publication, distribution, etc. Jan 1993
300 ## - PHYSICAL DESCRIPTION
Extent 152-7 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Arginine
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 Cysteine
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Erythrocytes, Abnormal
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Genotype
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Hematologic Diseases
General subdivision genetics
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 Mutation
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Polymorphism, Genetic
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Spectrin
General subdivision genetics
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Miraglia del Giudice, E
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Alloisio, N
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Morle, L
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Forissier, A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Perrotta, S
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Sciarratta, G
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Iolascon, A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Delaunay, J
773 0# - HOST ITEM ENTRY
Title British journal of haematology
Related parts vol. 83
-- no. 1
-- p. 152-7
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1111/j.1365-2141.1993.tb04646.x">https://doi.org/10.1111/j.1365-2141.1993.tb04646.x</a>
Public note Available from publisher's website

No items available.