Chromosome 15 in Prader-Willi syndrome. (Record no. 4024108)

MARC details
000 -LEADER
fixed length control field 01270 a2200397 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250512083755.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 198508s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0012-1622
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1111/j.1469-8749.1985.tb04540.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 Fear, C N
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 19850828
245 00 - TITLE STATEMENT
Title Chromosome 15 in Prader-Willi syndrome.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Developmental medicine and child neurology
Date of publication, distribution, etc. Jun 1985
300 ## - PHYSICAL DESCRIPTION
Extent 305-11 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 Child
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 Chromosome Aberrations
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chromosome Banding
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chromosome Deletion
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chromosome Disorders
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chromosomes, Human, 16-18
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 Infant
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 Prader-Willi Syndrome
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Translocation, Genetic
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Mutton, D E
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Berry, A C
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Heckmatt, J Z
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Dubowitz, V
773 0# - HOST ITEM ENTRY
Title Developmental medicine and child neurology
Related parts vol. 27
-- no. 3
-- p. 305-11
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1111/j.1469-8749.1985.tb04540.x">https://doi.org/10.1111/j.1469-8749.1985.tb04540.x</a>
Public note Available from publisher's website

No items available.