A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndrome. (Record no. 1669140)

MARC details
000 -LEADER
fixed length control field 01423 a2200421 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250511195934.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 199202s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 0888-7543
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1016/0888-7543(91)90105-n
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 Gemmill, R M
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 19920214
245 00 - TITLE STATEMENT
Title A 2.5-Mb physical map within 3p21.1 spans the breakpoint associated with Greig cephalopolysyndactyly syndrome.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Genomics
Date of publication, distribution, etc. Sep 1991
300 ## - PHYSICAL DESCRIPTION
Extent 93-102 p.
Other physical details digital
500 ## - GENERAL NOTE
General note Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Cell Line
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 Chromosomes, Human, Pair 3
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Electrophoresis, Gel, Pulsed-Field
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Facial Bones
General subdivision abnormalities
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Genetic Linkage
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 Skull
General subdivision abnormalities
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Syndactyly
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 Translocation, Genetic
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Varella-Garcia, M
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Smith, D I
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Erickson, P
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Golembieski, W
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Miller, Y
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Coyle-Morris, J
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Tommerup, N
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Drabkin, H A
773 0# - HOST ITEM ENTRY
Title Genomics
Related parts vol. 11
-- no. 1
-- p. 93-102
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1016/0888-7543(91)90105-n">https://doi.org/10.1016/0888-7543(91)90105-n</a>
Public note Available from publisher's website

No items available.