Literature DB >> 18325041

Mapping of a new autosomal recessive non-syndromic hearing impairment locus (DFNB45) to chromosome 1q43-q44.

A Bhatti, K Lee, M-L McDonald, M J Hassan, R Gutala, M Ansar, W Ahmad, S M Leal.   

Abstract

Entities:  

Mesh：

Year:  2008        PMID： 18325041      PMCID： PMC2747313          DOI： 10.1111/j.1399-0004.2008.00976.x

Source DB:  PubMed          Journal:  Clin Genet        ISSN： 0009-9163            Impact factor:   4.438


× No keyword cloud information.
  21 in total

1.  Allegro, a new computer program for multipoint linkage analysis.

Authors:  D F Gudbjartsson; K Jonasson; M L Frigge; A Kong
Journal:  Nat Genet       Date:  2000-05       Impact factor: 38.330

2.  Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.

Authors:  Gonçalo R Abecasis; Stacey S Cherny; William O Cookson; Lon R Cardon
Journal:  Nat Genet       Date:  2001-12-03       Impact factor: 38.330

3.  The human genome browser at UCSC.

Authors:  W James Kent; Charles W Sugnet; Terrence S Furey; Krishna M Roskin; Tom H Pringle; Alan M Zahler; David Haussler
Journal:  Genome Res       Date:  2002-06       Impact factor: 9.043

4.  A combined linkage-physical map of the human genome.

Authors:  X Kong; K Murphy; T Raj; C He; P S White; T C Matise
Journal:  Am J Hum Genet       Date:  2004-10-14       Impact factor: 11.025

5.  Analysis and functional evaluation of the hair-cell transcriptome.

Authors:  Brian M McDermott; Jessica M Baucom; A J Hudspeth
Journal:  Proc Natl Acad Sci U S A       Date:  2007-07-02       Impact factor: 11.205

Review 6.  Genetic epidemiology of hearing impairment.

Authors:  N E Morton
Journal:  Ann N Y Acad Sci       Date:  1991       Impact factor: 5.691

7.  Characterization of a novel human opsin gene with wide tissue expression and identification of embedded and flanking genes on chromosome 1q43.

Authors:  S Halford; M S Freedman; J Bellingham; S L Inglis; S Poopalasundaram; B G Soni; R G Foster; D M Hunt
Journal:  Genomics       Date:  2001-03-01       Impact factor: 5.736

8.  Incorrect specification of marker allele frequencies: effects on linkage analysis.

Authors:  N B Freimer; L A Sandkuijl; S M Blower
Journal:  Am J Hum Genet       Date:  1993-06       Impact factor: 11.025

9.  Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.

Authors:  Kiyoto Kurima; Linda M Peters; Yandan Yang; Saima Riazuddin; Zubair M Ahmed; Sadaf Naz; Deidre Arnaud; Stacy Drury; Jianhong Mo; Tomoko Makishima; Manju Ghosh; P S N Menon; Dilip Deshmukh; Carole Oddoux; Harry Ostrer; Shaheen Khan; Sheikh Riazuddin; Prescott L Deininger; Lori L Hampton; Susan L Sullivan; James F Battey; Bronya J B Keats; Edward R Wilcox; Thomas B Friedman; Andrew J Griffith
Journal:  Nat Genet       Date:  2002-02-19       Impact factor: 38.330

10.  Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.

Authors:  Saber Masmoudi; Abdelaziz Tlili; Marja Majava; Abdel Monem Ghorbel; Sébastien Chardenoux; Arnaud Lemainque; Zeineb Ben Zina; Jihene Moala; Minna Männikkö; Dominique Weil; Mark Lathrop; Leena Ala-Kokko; Mohamed Drira; Christine Petit; Hammadi Ayadi
Journal:  Eur J Hum Genet       Date:  2003-02       Impact factor: 4.246
View more
  1 in total

1.  Maternal interchromosomal insertional translocation leading to 1q43-q44 deletion and duplication in two siblings.

Authors:  Aixiang Luo; Dehua Cheng; Shimin Yuan; Haiyu Li; Juan Du; Yang Zhang; Chuanchun Yang; Ge Lin; Wenyong Zhang; Yue-Qiu Tan
Journal:  Mol Cytogenet       Date:  2018-04-04       Impact factor: 2.009
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.