Literature DB >> 222549

Assignment of alpha-galactosidase (alpha GAL) to the q22 leads to qter region of the X chromosome in man.

T B Shows, J A Brown, L L Haley, A P Goggin, R L Eddy, M G Byers.   

Abstract

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Year:  1978        PMID： 222549     DOI： 10.1159/000131020

Source DB:  PubMed          Journal:  Cytogenet Cell Genet        ISSN： 0301-0171


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  5 in total

Review 1.  Anderson-Fabry disease.

Authors:  S H Morgan; M A Crawfurd
Journal:  BMJ       Date:  1988-10-08

2.  X-autosome translocations: cytogenetic characteristics and their consequences.

Authors:  M G Mattei; J F Mattei; S Ayme; F Giraud
Journal:  Hum Genet       Date:  1982       Impact factor: 4.132

3.  Anderson Fabry disease, a close linkage with highly polymorphic DNA markers DXS17, DXS87 and DXS88.

Authors:  K D MacDermot; S H Morgan; J K Cheshire; T M Wilson
Journal:  Hum Genet       Date:  1987-11       Impact factor: 4.132

4.  Genetic screening of Fabry patients with EcoTILLING and HRM technology.

Authors:  Caterina Bono; Domenico Nuzzo; Giuseppe Albeggiani; Carmela Zizzo; Daniele Francofonte; Francesco Iemolo; Enzo Sanzaro; Giovanni Duro
Journal:  BMC Res Notes       Date:  2011-09-06

5.  Genotype: A Crucial but Not Unique Factor Affecting the Clinical Phenotypes in Fabry Disease.

Authors:  Xiaoxia Pan; Yan Ouyang; Zhaohui Wang; Hong Ren; Pingyan Shen; Weiming Wang; Yaowen Xu; Liyan Ni; Xialian Yu; Xiaonong Chen; Wen Zhang; Li Yang; Xiao Li; Jing Xu; Nan Chen
Journal:  PLoS One       Date:  2016-08-25       Impact factor: 3.240
  5 in total

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