GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss. (Record no. 11869735)

MARC details
000 -LEADER
fixed length control field 01429 a2200421 4500
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250514031518.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 200206s 0 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1098-1004
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1002/humu.9033
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 Najmabadi, Hossein
264 #0 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Date of production, publication, distribution, manufacture, or copyright notice 20020627
245 00 - TITLE STATEMENT
Title GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.
Medium [electronic resource]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Name of publisher, distributor, etc. Human mutation
Date of publication, distribution, etc. May 2002
300 ## - PHYSICAL DESCRIPTION
Extent 572 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 Connexin 26
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Connexins
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Genes, Recessive
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Genetic Carrier Screening
General subdivision methods
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Genetic Testing
General subdivision methods
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Hearing Disorders
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 Iran
General subdivision epidemiology
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Mutation
General subdivision genetics
650 04 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Syndrome
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Cucci, Robert A
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Sahebjam, Solmaz
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kouchakian, Nafiseh
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Farhadi, Mohammad
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Kahrizi, Kimia
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Arzhangi, Sanaz
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Daneshmandan, Naiimeh
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Javan, Khalil
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Smith, Richard J H
773 0# - HOST ITEM ENTRY
Title Human mutation
Related parts vol. 19
-- no. 5
-- p. 572
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://doi.org/10.1002/humu.9033">https://doi.org/10.1002/humu.9033</a>
Public note Available from publisher's website

No items available.