Literature DB >> 3568428

Fragile 19p13 in a family with mental illness.

B N Chodirker, A E Chudley, M Ray, D E Wickstrom, D L Riordan.   

Abstract

We describe a family where four brothers show the rare heritable folate sensitive autosomal fragile site (FSAFS) at 19p13 when cells were grown in TC199. Two of the brothers are schizophrenic while one brother is mentally retarded with autistic-like features. The clinical significance of this fragile site however is still unknown.

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Year:  1987        PMID： 3568428     DOI： 10.1111/j.1399-0004.1987.tb02759.x

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


  5 in total

1.  Peutz-Jeghers syndrome diagnosed in a schizophrenic patient with a large deletion in the STK11 gene.

Authors:  Michael Kam; Jorge Massare; Steven Gallinger; Joseph Kinzie; Donald Weaver; John D Dingell; Susmita Esufali; Bharati Bapat; Martin Tobi
Journal:  Dig Dis Sci       Date:  2006-08-22       Impact factor: 3.199

2.  Population cytogenetics of rare fragile sites in Japan.

Authors:  E Takahashi; T Hori; M Murata
Journal:  Hum Genet       Date:  1988-02       Impact factor: 4.132

3.  ICF syndrome with variable expression in sibs.

Authors:  G Gimelli; P Varone; A Pezzolo; M Lerone; V Pistoia
Journal:  J Med Genet       Date:  1993-05       Impact factor: 6.318

Review 4.  Chromosome abnormalities, mental retardation and the search for genes in bipolar disorder and schizophrenia.

Authors:  D H R Blackwood; T Thiagarajah; P Malloy; B S Pickard; W J Muir
Journal:  Neurotox Res       Date:  2008-10       Impact factor: 3.911

Review 5.  Chromosomal aberrations and schizophrenia. Autosomes.

Authors:  A S Bassett
Journal:  Br J Psychiatry       Date:  1992-09       Impact factor: 9.319
  5 in total

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