A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH. (Record no. 17453422)

MARC details
000 -LEADER
fixed length control field 01548 a2200433 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250515091534.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200901s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0340-6199
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1007/s00431-007-0616-7
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 Klopocki, Eva
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20090106
245 00 - TITLE STATEMENT
Title A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. European journal of pediatrics
Date of publication, distribution, etc. Aug 2008
300 ## - PHYSICAL DESCRIPTION
Extent 903-8 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 Child
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, Artificial, Bacterial
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chromosomes, Human, Pair 15
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Comparative Genomic Hybridization
General subdivision methods
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 Developmental Disabilities
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Fingers
General subdivision abnormalities
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Gene Dosage
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 In Situ Hybridization, Fluorescence
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 Penis
General subdivision abnormalities
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Graul-Neumann, Luitgard M
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Grieben, Ulrike
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Tönnies, Holger
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Ropers, Hans-Hilger
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Horn, Denise
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Mundlos, Stefan
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Ullmann, Reinhard
773 0# - HOST ITEM ENTRY
Title European journal of pediatrics
Related parts vol. 167
-- no. 8
-- p. 903-8
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1007/s00431-007-0616-7">https://doi.org/10.1007/s00431-007-0616-7</a>
Public note Available from publisher's website

No items available.