Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief review. (Record no. 9197524)

MARC details
000 -LEADER
fixed length control field 01465 a2200397 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250513122241.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 199709s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0148-7299
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1002/(sici)1096-8628(19970808)71:2<189::aid-ajmg13>3.0.co;2-a
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 Stockton, D W
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 19970903
245 00 - TITLE STATEMENT
Title Severe clinical phenotype due to an interstitial deletion of the short arm of chromosome 1: a brief review.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. American journal of medical genetics
Date of publication, distribution, etc. Aug 1997
300 ## - PHYSICAL DESCRIPTION
Extent 189-93 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 Abnormalities, Multiple
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 Chromosomes, Human, Pair 1
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Craniofacial Abnormalities
General subdivision genetics
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 Hand Deformities, Congenital
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Heart Defects, Congenital
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 Infant, Newborn
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Karyotyping
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Phenotype
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Ross, H L
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Bacino, C A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Altman, C A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Shaffer, L G
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Lupski, J R
773 0# - HOST ITEM ENTRY
Title American journal of medical genetics
Related parts vol. 71
-- no. 2
-- p. 189-93
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1002/(sici)1096-8628(19970808)71:2<189::aid-ajmg13>3.0.co;2-a">https://doi.org/10.1002/(sici)1096-8628(19970808)71:2<189::aid-ajmg13>3.0.co;2-a</a>
Public note Available from publisher's website

No items available.