Exclusion of familial dysautonomia from more than 60% of the genome.-Reference-Cited by-同舟云学术

Exclusion of familial dysautonomia from more than 60% of the genome.

Published:1993-01-01 Issue:1 Volume:30 Page:47-52
ISSN:1468-6244
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Blumenfeld A,Axelrod F B,Trofatter J A,Maayan C,Lucente D E,Slaugenhaupt S A,Liebert C B,Ozelius L J,Haines J L,Breakefield X O

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference26 articles.

1. Central autonomic dysfunction with defective lacrimation;Riley, C.M.; Day, R.L.; DMcL, Greely; Langford, W.S.;Pediatrics,1949

2. Congenital sensory neuropathies. Diagnostic distinction from familial dysautonomia;Axelrod, F.B.; Pearson, J.;Am Jf Dis Child,1984

3. Familial dysautonomia and other congenital sensory and autonomic neuropathies;Axelrod, F.B.,1984

4. Structural gene for n-nerve growth factor not defective;Breakefield, X.O.; Orloff, G.; Castiglione, C.; Coussens, L.; Axelrod, F.B.; Ullrich, A.,1984

5. DNA polymorphisms for the nerve growth factor receptor gene exclude its role in familial dysautonomia;Breakefield, X.O.; Ozelius, L.; Bothwell, M.A.;Mol Biol Med,1986

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1. Hereditary dysautonomias: current knowledge and collaborations for the future;Clinical Autonomic Research;2003-06

2. Lexikalischer Teil;Lexikon der Syndrome und Fehlbildungen;2003

3. Precise Genetic Mapping and Haplotype Analysis of the Familial Dysautonomia Gene on Human Chromosome 9q31;The American Journal of Human Genetics;1999-04

4. Lexikon der Syndrome und Fehlbildungen;Lexikon der Syndrome und Fehlbildungen;1999

5. Decreased incorporation ofd-glucosamine into glycosphingolipids of intact familial dysautonomia lymphoblasts;Journal of Molecular Neuroscience;1995-06