Literature DB >> 7717411

Deletion mapping of X-linked mixed deafness (DFN3) identifies a 265-525-kb region centromeric of DXS26.

N Dahl, J Laporte, L Hu, V Biancalana, D Le Palier, D Cohen, C Piussan, J L Mandel.   

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Year:  1995        PMID： 7717411      PMCID： PMC1801217     

Source DB:  PubMed          Journal:  Am J Hum Genet        ISSN： 0002-9297            Impact factor:   11.025


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  15 in total

1.  Continuum of overlapping clones spanning the entire human chromosome 21q.

Authors:  I Chumakov; P Rigault; S Guillou; P Ougen; A Billaut; G Guasconi; P Gervy; I LeGall; P Soularue; L Grinas
Journal:  Nature       Date:  1992-10-01       Impact factor: 49.962

2.  Phenotypic evidence for a common pathogenesis in X-linked deafness pedigrees and in Xq13-q21 deletion related deafness.

Authors:  W Reardon; S Roberts; P D Phelps; N S Thomas; L Beck; R Issac; H E Hughes
Journal:  Am J Med Genet       Date:  1992-11-01

3.  Physical fine mapping of genes underlying X-linked deafness and non fra (X)-X-linked mental retardation at Xq21.

Authors:  I Bach; D Robinson; N Thomas; H H Ropers; F P Cremers
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

4.  Alu-primed polymerase chain reaction for regional assignment of 110 yeast artificial chromosome clones from the human X chromosome: identification of clones associated with a disease locus.

Authors:  D L Nelson; A Ballabio; M F Victoria; M Pieretti; R D Bies; R A Gibbs; J A Maley; A C Chinault; T D Webster; C T Caskey
Journal:  Proc Natl Acad Sci U S A       Date:  1991-07-15       Impact factor: 11.205

5.  Choroideremia, obesity, and congenital deafness.

Authors:  S Ayazi
Journal:  Am J Ophthalmol       Date:  1981-07       Impact factor: 5.258

6.  Sex linked deafness: Wilde revisited.

Authors:  W Reardon
Journal:  J Med Genet       Date:  1990-06       Impact factor: 6.318

7.  A multipedigree linkage study of X-linked deafness: linkage to Xq13-q21 and evidence for genetic heterogeneity.

Authors:  W Reardon; H R Middleton-Price; L Sandkuijl; P Phelps; S Bellman; L Luxon; M E Pembrey; S Malcolm
Journal:  Genomics       Date:  1991-12       Impact factor: 5.736

8.  Isolation of anonymous DNA sequences from within a submicroscopic X chromosomal deletion in a patient with choroideremia, deafness, and mental retardation.

Authors:  R L Nussbaum; J G Lesko; R A Lewis; S A Ledbetter; D H Ledbetter
Journal:  Proc Natl Acad Sci U S A       Date:  1987-09       Impact factor: 11.205

9.  Choroideremia, congenital deafness and mental retardation in a family with an X chromosomal deletion.

Authors:  T Rosenberg; E Niebuhr; H M Yang; A Parving; M Schwartz
Journal:  Ophthalmic Paediatr Genet       Date:  1987-11

10.  X-linked mixed deafness (DFN3): cloning and characterization of the critical region allows the identification of novel microdeletions.

Authors:  I Huber; M Bitner-Glindzicz; Y J de Kok; S M van der Maarel; Y Ishikawa-Brush; A P Monaco; D Robinson; S Malcolm; M E Pembrey; H G Brunner
Journal:  Hum Mol Genet       Date:  1994-07       Impact factor: 6.150
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  2 in total

1.  Characterisation and genetic mapping of a new X linked deafness syndrome.

Authors:  D M Martin; F J Probst; S A Camper; E M Petty
Journal:  J Med Genet       Date:  2000-11       Impact factor: 6.318

2.  Refinement of the locus for non-syndromic sensorineural deafness (DFN2).

Authors:  Bin Cui; Haibing Zhang; Yongzhong Lu; Wei Zhong; Gang Pei; Xiangyin Kong; Landian Hu
Journal:  J Genet       Date:  2004-04       Impact factor: 1.166
  2 in total

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