An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS. (Record no. 8741054)

MARC details
000 -LEADER
fixed length control field 01486 a2200445 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250513094518.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 199611s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1018-4813
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1159/000472177
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 Van de Vosse, E
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 19961112
245 00 - TITLE STATEMENT
Title An Xp22.1-p22.2 YAC contig encompassing the disease loci for RS, KFSD, CLS, HYP and RP15: refined localization of RS.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. European journal of human genetics : EJHG
Date of publication, distribution, etc. 1996
300 ## - PHYSICAL DESCRIPTION
Extent 101-4 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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 Mapping
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Chromosomes, Artificial, Yeast
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Darier Disease
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 Humans
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Hypophosphatemia, Familial
General subdivision genetics
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 Pedigree
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Retinal Degeneration
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Syndrome
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element X Chromosome
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Bergen, A A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Meershoek, E J
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Oosterwijk, J C
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Gregory, S
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Bakker, B
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Weissenbach, J
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Coffey, A J
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name van Ommen, G J
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Den Dunnen, J T
773 0# - HOST ITEM ENTRY
Title European journal of human genetics : EJHG
Related parts vol. 4
-- no. 2
-- p. 101-4
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1159/000472177">https://doi.org/10.1159/000472177</a>
Public note Available from publisher's website

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