Literature DB >> 457128

Fragile site long arm chromosome 16.

K Sørensen, J Nielsen, V Holm, J Haahr.   

Abstract

A fragile site at the long arms (q21) of chromosome 16 was found in two persons, each of whom became the parent of a child with a de novo structural chromosome abnormality--a balanced autosomal translocation and an autosomal deletion. The question of an increased risk of structural chromosome abnormalities in the offspring of persons with fragile site long arm 16 is discussed.

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Year:  1979        PMID: 457128     DOI: 10.1007/bf00273287

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


  9 in total

1.  [Interstitial deletion of the long arm of one 11 chromosome].

Authors:  J L Taillemite; B G Morlier; C Roux
Journal:  Ann Genet       Date:  1975-03

2.  The 11q-- syndrome: another case report.

Authors:  M T Mulcahy; J Jenkyn
Journal:  Hum Genet       Date:  1977-04-15       Impact factor: 4.132

Review 3.  Induced chromosomal aberrations: biological and clinical significance.

Authors:  A D Bloom
Journal:  J Pediatr       Date:  1972-07       Impact factor: 4.406

4.  An (11;21) translocation in four generations with chromosome 11 abnormalities in the offspring. A clinical, cytogenetical, and gene marker study.

Authors:  P Jacobsen; M Hauge; K Henningsen; N Hobolth; M Mikkelsen; J Philip
Journal:  Hum Hered       Date:  1973       Impact factor: 0.444

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.  Spontaneous chromosomal breakage and high incidence of leukemia in inherited disease.

Authors:  T M Schroeder; R Kurth
Journal:  Blood       Date:  1971-01       Impact factor: 22.113

7.  The interaction of various drugs with human chromosomes.

Authors:  M M Cohen
Journal:  Can J Genet Cytol       Date:  1969-03

8.  Apparently spontaneous chromosome damage in human leukocytes and the nature of chromatid gaps.

Authors:  A Brogger
Journal:  Humangenetik       Date:  1971

9.  Apparently balanced de novo translocations in patients with abnormal phenotypes: report of 6 cases.

Authors:  A T Tharapel; R L Summitt; R S Wilroy; P Martens
Journal:  Clin Genet       Date:  1977-04       Impact factor: 4.438

  9 in total
  8 in total

1.  The fragile site (16) (q22). I. Induction by AT-specific DNA-ligands and population frequency.

Authors:  M Schmid; W Feichtinger; A Jessberger; J Köhler; R Lange
Journal:  Hum Genet       Date:  1986-09       Impact factor: 4.132

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

Authors:  J M García-Sagredo; C San Román; M E Gallego Gómez; G Lledo
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

3.  Familial fragility on chromosome 16 (fra 16q22) enhanced by both interferon and Distamycin A.

Authors:  F Shabtai; D Klar; S Bichacho; J Hart; I Halbrecht
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

4.  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

5.  Disease associated balanced chromosome rearrangements: a resource for large scale genotype-phenotype delineation in man.

Authors:  M Bugge; G Bruun-Petersen; K Brøndum-Nielsen; U Friedrich; J Hansen; G Jensen; P K Jensen; U Kristoffersson; C Lundsteen; E Niebuhr; K R Rasmussen; K Rasmussen; N Tommerup
Journal:  J Med Genet       Date:  2000-11       Impact factor: 6.318

6.  The use of distamycin A in human lymphocyte cultures.

Authors:  M Schmid; D A Hungerford; A Poppen; W Engel
Journal:  Hum Genet       Date:  1984       Impact factor: 4.132

7.  Interstitial deletion of the long arm of chromosome 11.

Authors:  J M Klep-de Pater; H F de France; J B Bijlsma
Journal:  J Med Genet       Date:  1985-06       Impact factor: 6.318

Review 8.  Partial trisomy 16q21➔qter due to an unbalanced segregation of a maternally inherited balanced translocation 46,XX,t(15;16)(p13;q21): a case report and review of literature.

Authors:  R Mishra; C S Paththinige; N D Sirisena; S Nanayakkara; U G I U Kariyawasam; V H W Dissanayake
Journal:  BMC Pediatr       Date:  2018-01-08       Impact factor: 2.125

  8 in total

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