Floating-Harbor syndrome: SRCAP mutations are not restricted to exon 34. (Record no. 22832923)

MARC details
000 -LEADER
fixed length control field 01210 a2200385 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250516154145.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 201411s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1399-0004
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1111/cge.12199
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 Kehrer, M
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20141121
245 00 - TITLE STATEMENT
Title Floating-Harbor syndrome: SRCAP mutations are not restricted to exon 34.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Clinical genetics
Date of publication, distribution, etc. May 2014
300 ## - PHYSICAL DESCRIPTION
Extent 498-9 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Case Reports; Letter
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 Adenosine Triphosphatases
General subdivision genetics
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 Craniofacial Abnormalities
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Exons
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Growth Disorders
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Heart Septal Defects, Ventricular
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
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Beckmann, A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Wyduba, J
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Finckh, U
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Dufke, A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Gaiser, U
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Tzschach, A
773 0# - HOST ITEM ENTRY
Title Clinical genetics
Related parts vol. 85
-- no. 5
-- p. 498-9
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1111/cge.12199">https://doi.org/10.1111/cge.12199</a>
Public note Available from publisher's website

No items available.