Further observations on a previously reported case of 4p--syndrome. (Record no. 4638264)
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000 -LEADER | |
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fixed length control field | 01002 a2200313 4500 |
005 - DATE AND TIME OF LATEST TRANSACTION | |
control field | 20250512120102.0 |
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION | |
fixed length control field | 197301s 0 0 eng d |
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER | |
International Standard Serial Number | 0018-7348 |
024 7# - OTHER STANDARD IDENTIFIER | |
Standard number or code | 10.1007/BF00281740 |
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 | Subrt, I |
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE | |
Date of production, publication, distribution, manufacture, or copyright notice | 19730129 |
245 00 - TITLE STATEMENT | |
Title | Further observations on a previously reported case of 4p--syndrome. |
Medium | [electronic resource] |
260 ## - PUBLICATION, DISTRIBUTION, ETC. | |
Name of publisher, distributor, etc. | Humangenetik |
Date of publication, distribution, etc. | 1972 |
300 ## - PHYSICAL DESCRIPTION | |
Extent | 361-3 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 | Abnormalities, Multiple |
General subdivision | genetics |
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 |
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, 4-5 |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Cri-du-Chat Syndrome |
General subdivision | genetics |
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM | |
Topical term or geographic name entry element | Fluorescence |
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 |
700 1# - ADDED ENTRY--PERSONAL NAME | |
Personal name | Blehová, B |
773 0# - HOST ITEM ENTRY | |
Title | Humangenetik |
Related parts | vol. 15 |
-- | no. 4 |
-- | p. 361-3 |
856 40 - ELECTRONIC LOCATION AND ACCESS | |
Uniform Resource Identifier | <a href="https://doi.org/10.1007/BF00281740">https://doi.org/10.1007/BF00281740</a> |
Public note | Available from publisher's website |
No items available.