Literature DB >> 6654336

Fragile chromosome 16(q22) cause a balanced translocation at the same point.

J M García-Sagredo, C San Román, M E Gallego Gómez, G Lledo.   

Abstract

A father with a fragile 16(q22) has a son with a de novo balanced translocation 1;16. Both the fragile site and the break point at chromosome 16 are similar (q22). The question of whether the fragile site can cause a structural chromosome abnormality at the same point is discussed.

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Year:  1983        PMID： 6654336     DOI： 10.1007/BF00286668

Source DB:  PubMed          Journal:  Hum Genet        ISSN： 0340-6717            Impact factor:   4.132


  11 in total

1.  Cytogenetic investigation in 413 couples with spontaneous abortions.

Authors:  C Turleau; F Chavin-Colin; J de Grouchy
Journal:  Eur J Obstet Gynecol Reprod Biol       Date:  1979-04       Impact factor: 2.435

2.  A cascade of chromosomal aberrations in three generations: a fragile 16q, an extra fragment and a rearranged 20.

Authors:  G B Côté; S Papadakou-Lagoyanni; S Pantelakis
Journal:  Ann Genet       Date:  1978-12

3.  Deleted chromosome 18 with paternal mosaicism.

Authors:  E J Day; R Marshall; P A MacDonald; W M Davidson
Journal:  Lancet       Date:  1967-12-16       Impact factor: 79.321

4.  Double heteroploidy, 46, XY, t(13q14q), +18, in a spontaneous abortus.

Authors:  S Avirachan; T Kajii
Journal:  Clin Genet       Date:  1973       Impact factor: 4.438

5.  Heritable fragile site on chromosome 16: probable localization of haptoglobin locus in man.

Authors:  R E Magenis; F Hecht; E W Lovrien
Journal:  Science       Date:  1970-10-02       Impact factor: 47.728

6.  Constitutional chromosomal breakage.

Authors:  F Giraud; S Ayme; J F Mattei; M G Mattei
Journal:  Hum Genet       Date:  1976-10-28       Impact factor: 4.132

7.  The fragile site on chromosome 16 (q21q22). Data on four new families.

Authors:  F Shabtai; S Bichacho; I Halbrecht
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

8.  Fragile site long arm chromosome 16.

Authors:  K Sørensen; J Nielsen; V Holm; J Haahr
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

9.  Abnormal childhood phenotypes associated with the same balanced chromosome rearrangements as in the parents.

Authors:  S Ayme; M G Mattei; J F Mattei; F Giraud
Journal:  Hum Genet       Date:  1979-04-17       Impact factor: 4.132

10.  Systematic analysis of 95 reciprocal translocations of autosomes.

Authors:  A Aurias; M Prieur; B Dutrillaux; J Lejeune
Journal:  Hum Genet       Date:  1978-12-29       Impact factor: 4.132
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  6 in total

Review 1.  Balanced translocations in mental retardation.

Authors:  Geert Vandeweyer; R Frank Kooy
Journal:  Hum Genet       Date:  2009-04-05       Impact factor: 4.132

2.  Chromosome deletion at 11q23 in an abnormal child from a family with inherited fragility at 11q23.

Authors:  L E Voullaire; G C Webb; M A Leversha
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

3.  Autosomal fragile sites not a current indication for prenatal diagnosis.

Authors:  F Hecht; B K Hecht
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

4.  Expression of fragile sites in human sperm and lymphocyte chromosomes.

Authors:  J Benet; C Fuster; A Genescà; J Navarro; R Miró; J Egozcue; C Templado
Journal:  Hum Genet       Date:  1989-02       Impact factor: 4.132

5.  Familial fragile site found at the cancer breakpoint (1)(q32). Inducibility by distamycin A, concomitance with fragile (16)(q22).

Authors:  F Shabtai; J Hart; D Klar; I Halbrecht
Journal:  Hum Genet       Date:  1986-07       Impact factor: 4.132

6.  De novo c.2455C>T mutation of NPR2 gene in a fetus with shortened long bones and a ventricular septal defect conceived by a mother with a fragile site at 16q22.1 and a father with a rare heterochromatic variant of chromosome 4 from Vietnam.

Authors:  Thi Minh Thi Ha; Tran Thao Nguyen Nguyen; Thi Mai Ngan Nguyen; Huu Nguyen Nguyen
Journal:  Mol Genet Genomic Med       Date:  2021-03-13       Impact factor: 2.183
  6 in total

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