Literature DB >> 6467665

Fragile 22q13 segregating in a family.

T Webb, A Thake.   

Abstract

During the course of a population study of non-specific mental retardation in school-age males, a 13-year-old boy was ascertained. Cytogenetic studies revealed the presence of a fragile site at chromosome 22. The site was found to be both folate-dependent and heritable. The possibility that the presence of this fragile site is linked to mental retardation is discussed.

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Mesh：

Year:  1984        PMID： 6467665     DOI： 10.1111/j.1399-0004.1984.tb00801.x

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


  3 in total

1.  Studies on three rare fragile sites. 2q13, 12q13, and 17p12 segregating in one family.

Authors:  D R Romain; L M Columbano-Green; R H Smythe; R G Parfitt; O B Gebbie; C J Chapman
Journal:  Hum Genet       Date:  1986-06       Impact factor: 4.132

2.  A heritable fragile 12q24.13 segregating in a family with the fragile X chromosome.

Authors:  A P Amarose; P R Huttenlocher; R M Sprudzs; T J Laitsch; M J Pettenati
Journal:  Hum Genet       Date:  1987-01       Impact factor: 4.132

Review 3.  Fragility Extraordinaire: Unsolved Mysteries of Chromosome Fragile Sites.

Authors:  Wenyi Feng; Arijita Chakraborty
Journal:  Adv Exp Med Biol       Date:  2017       Impact factor: 2.622
  3 in total

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